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<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Front matter</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J296800FP001</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>P001</fpage>
<lpage>P002</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J296800FP001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J296800FP001">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Front matter</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J296800FP003</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>P003</fpage>
<lpage>P004</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J296800FP003">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J296800FP003">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The fragmentation of some 2-pyridones, 2-pyridthiones, and 2-alkylthiopyridines induced by electron impact</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000001</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lawrence</surname>
<given-names>R.</given-names></name>
<name><surname>Waight</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1</fpage>
<lpage>6</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000001">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitramines and nitramides. Part XIII. Nuclear magnetic resonance spectra</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000006</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lamberton</surname>
<given-names>Alex. H.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>I. O.</given-names></name>
<name><surname>Thorpe</surname>
<given-names>J. E.</given-names></name>
<name><surname>Yusuf</surname>
<given-names>H. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>6</fpage>
<lpage>8</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000006">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000006">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular conformations. Part IV. &lt;i&gt;X&lt;/i&gt;-Ray analysis of 3β,6β-dimethoxy-5β,19-cycloandrostan-17-one &lt;i&gt;N&lt;/i&gt;-acetyl-&lt;i&gt;p&lt;/i&gt;-bromobenzenesulphonylhydrazone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000008</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tamura</surname>
<given-names>Chihiro</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>8</fpage>
<lpage>15</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000008">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000008">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron-impact studies. Part XXI. The mass spectra of sulphonamides and sulphonyl chlorides: the formation of C–O and C–N bonds upon electron impact</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000015</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dynesen</surname>
<given-names>E.</given-names></name>
<name><surname>Lawesson</surname>
<given-names>S.-O.</given-names></name>
<name><surname>Schroll</surname>
<given-names>G.</given-names></name>
<name><surname>Bowie</surname>
<given-names>J. H.</given-names></name>
<name><surname>Cooks</surname>
<given-names>R. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>15</fpage>
<lpage>21</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000015">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000015">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular photoelectron spectroscopy. Part VII. The vertical ionisation potentials of benzene and some of its monosubstituted and 1,4-disubstituted derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000022</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baker</surname>
<given-names>A. D.</given-names></name>
<name><surname>May</surname>
<given-names>D. P.</given-names></name>
<name><surname>Turner</surname>
<given-names>D. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>22</fpage>
<lpage>34</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000022">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000022">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Fragmentation of organic molecules under electron impact. Part 1. Ureas</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000034</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baldwin</surname>
<given-names>M. A.</given-names></name>
<name><surname>Kirkien-Konasiewicz</surname>
<given-names>(Mrs.) Alicja M.</given-names></name>
<name><surname>Loudon</surname>
<given-names>A. G.</given-names></name>
<name><surname>Maccoll</surname>
<given-names>Allan</given-names></name>
<name><surname>Smith</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>34</fpage>
<lpage>40</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000034">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000034">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thermal rearrangement of diphenyl carbonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000040</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davis</surname>
<given-names>A.</given-names></name>
<name><surname>Golden</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>40</fpage>
<lpage>45</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000040">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000040">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thermal degradation of polycarbonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000045</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davis</surname>
<given-names>A.</given-names></name>
<name><surname>Golden</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>45</fpage>
<lpage>47</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000045">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000045">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance studies. Part XIV. Hydroxylation. Part III. Reactions of anisole, acetanilide, fluorobenzene, and some phenols with the titanium(III)–hydrogen peroxide system</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000048</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jefcoate</surname>
<given-names>C. R. E.</given-names></name>
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>48</fpage>
<lpage>53</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000048">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000048">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation. Part XXIII. Cyclic transition states in acylation by ketens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000054</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lillford</surname>
<given-names>P. J.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>54</fpage>
<lpage>57</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000054">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000054">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cycloadditions of the 2-methylallyl cation to conjugated dienes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000057</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hoffmann</surname>
<given-names>H. M. R.</given-names></name>
<name><surname>Joy</surname>
<given-names>D. R.</given-names></name>
<name><surname>Suter</surname>
<given-names>A. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>57</fpage>
<lpage>59</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000057">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000057">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electrochemical reactions. Part III. The reduction of benzyl bromides at a mercury cathode</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000060</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grimshaw</surname>
<given-names>J.</given-names></name>
<name><surname>Ramsey</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>60</fpage>
<lpage>62</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000060">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000060">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electrochemical reactions. Part IV. The polarography of substituted benzyltriphenylphosphonium salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000063</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grimshaw</surname>
<given-names>J.</given-names></name>
<name><surname>Ramsey</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>63</fpage>
<lpage>64</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000063">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000063">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism of benzidine and semidine rearrangements. Part XVI. Transitional kinetics in the acid rearrangement of 2-methoxyhydrazobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000064</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banthorpe</surname>
<given-names>D. V.</given-names></name>
<name><surname>Ingold</surname>
<given-names>Sir Christopher</given-names></name>
<name><surname>Roy</surname>
<given-names>Jyotibhushan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>64</fpage>
<lpage>66</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000064">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000064">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intramolecular reactions. Part VI. Rates of ring formation in reactions of ω-halogenoalkylmalonic esters with bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000067</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Knipe</surname>
<given-names>A. C.</given-names></name>
<name><surname>Stirling</surname>
<given-names>C. J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>67</fpage>
<lpage>71</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000067">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000067">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acyl trifluoroacetates. Part III. Trifluoroacetylation of hydroxy-groups with acetyl trifluoroacetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000072</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bonner</surname>
<given-names>T. G.</given-names></name>
<name><surname>Gabb</surname>
<given-names>E. G.</given-names></name>
<name><surname>McNamara</surname>
<given-names>P. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>72</fpage>
<lpage>75</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000072">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000072">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reduction of tetraphenylallene and related compounds in aprotic solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000075</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dietz</surname>
<given-names>R.</given-names></name>
<name><surname>Peover</surname>
<given-names>M. E.</given-names></name>
<name><surname>Wilson</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>75</fpage>
<lpage>80</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000075">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000075">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The study of conformational changes in 4,5-disubstituted phenanthrenes by nuclear magnetic resonance spectroscopy</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000080</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Munday</surname>
<given-names>R.</given-names></name>
<name><surname>Sutherland</surname>
<given-names>I. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>80</fpage>
<lpage>84</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000080">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000080">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance study of radicals photolytically generated from aromatic carbonyl compounds. The diphenylhydroxymethyl and α-hydroxybenzyl radicals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000084</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wilson</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>84</fpage>
<lpage>90</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000084">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000084">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The mechanism of oxidation of α-glycols by periodic acid. Part VIII. Oxidation of phenylethane-1,2-diol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000090</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buist</surname>
<given-names>G. J.</given-names></name>
<name><surname>Lewis</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>90</fpage>
<lpage>92</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000090">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000090">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics and mechanism of the formation of diaryliodonium salts by sulphuric acid catalysed reaction of substituted phenyl iodosoacetates with aromatic hydrocarbons in acetic acid solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000093</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Briody</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>93</fpage>
<lpage>98</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000093">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000093">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The kinetics and mechanism of the acid-catalysed hydrolysis of nitroalkanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000098</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cundall</surname>
<given-names>R. B.</given-names></name>
<name><surname>Locke</surname>
<given-names>A. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>98</fpage>
<lpage>103</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000098">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000098">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The mass spectra of tricarbonylcyclohexa-1,3-dieneiron derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000104</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Haas</surname>
<given-names>M. A.</given-names></name>
<name><surname>Wilson</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>104</fpage>
<lpage>107</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000104">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000104">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of radical anions. Part VI. The transfer of an electron to the tolan radical anion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000107</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dadley</surname>
<given-names>D. A.</given-names></name>
<name><surname>Evans</surname>
<given-names>Alwyn G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>107</fpage>
<lpage>111</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000107">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000107">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intramolecular reactions. Part VII. Cyclisation of aryl 3-chloropropyl sulphones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000111</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bird</surname>
<given-names>R.</given-names></name>
<name><surname>Stirling</surname>
<given-names>C. J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>111</fpage>
<lpage>114</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000111">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000111">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acyl trifluoroacetates. Part IV. Trifluoroacetylation of hydroxy-compounds with trifluoroacetic anhydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000114</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bonner</surname>
<given-names>T. G.</given-names></name>
<name><surname>McNamara</surname>
<given-names>P. M.</given-names></name>
<name><surname>Smethurst</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>114</fpage>
<lpage>118</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000114">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000114">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The infrared spectra and vibrational assignments of the acetyl halides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000118</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ramsey</surname>
<given-names>J. A.</given-names></name>
<name><surname>Ladd</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>118</fpage>
<lpage>122</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000118">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000118">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance studies. Part XV. Iminoxy-radicals from acetophenone oxime and related oximes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000123</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gilbert</surname>
<given-names>B. C.</given-names></name>
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>123</fpage>
<lpage>130</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000123">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000123">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photosensitised reactions of α-pinene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000130</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Frank</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>130</fpage>
<lpage>132</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000130">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000130">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nuclear magnetic resonance spectra of acetylacetaldehyde and malondialdehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000132</article-id><contrib-group><contrib contrib-type="author">
<name><surname>George</surname>
<given-names>W. O.</given-names></name>
<name><surname>Mansell</surname>
<given-names>V. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>132</fpage>
<lpage>134</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000132">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000132">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactivity of phosphate esters: reactions of monoesters with nucleophiles. Nucleophilicity independent of basicity in a bimolecular substitution reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000135</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kirby</surname>
<given-names>A. J.</given-names></name>
<name><surname>Varvoglis</surname>
<given-names>A. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>135</fpage>
<lpage>141</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000135">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000135">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Halide exchange at a saturated carbon atom in dimethylformamide solvent. Comparison of experimental rates and Arrhenius parameters with values calculated by Ingold</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000142</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cook</surname>
<given-names>D.</given-names></name>
<name><surname>Parker</surname>
<given-names>A. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>142</fpage>
<lpage>148</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000142">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000142">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The configurations of some weak complexes of benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000148</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Radford</surname>
<given-names>D. V.</given-names></name>
<name><surname>Ritchie</surname>
<given-names>G. L. D.</given-names></name>
<name><surname>Stiles</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>148</fpage>
<lpage>156</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000148">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000148">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The separation of polar and steric effects. Part VI. The kinetics of the acid-catalysed esterification of substituted benzoic acids by methanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000157</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Rodgers</surname>
<given-names>M. G.</given-names></name>
<name><surname>Shorter</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>157</fpage>
<lpage>164</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000157">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000157">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The separation of polar and steric effects. Part VII. The kinetics of the acid-catalysed esterification of substituted phenylacetic acids by methanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000164</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Rodgers</surname>
<given-names>M. G.</given-names></name>
<name><surname>Shorter</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>164</fpage>
<lpage>167</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000164">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000164">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stability of &lt;i&gt;N&lt;/i&gt;-heterocyclic oxime derivatives. Part III. The kinetics of the hydrolysis of formyl- and acetyl-pyridine &lt;i&gt;O&lt;/i&gt;-acetyloximes in aqueous solution in the pH range 6·0–10·8 at 25, 35, and 40°</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000167</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blanch</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>167</fpage>
<lpage>169</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000167">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000167">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stability of &lt;i&gt;N&lt;/i&gt;-heterocyclic oxime derivatives. Part IV. The kinetics of the sodium hydroxide-catalysed hydrolysis of phosphonylated ketoximes in water at 15, 20, 25, and 30°</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000169</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blanch</surname>
<given-names>J. H.</given-names></name>
<name><surname>Andersen</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>169</fpage>
<lpage>173</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000169">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000169">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The proton magnetic resonance spectrum of propiolactone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000173</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abraham</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>173</fpage>
<lpage>174</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000173">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000173">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of carbonyl compounds in basic solutions. Part I. The alkaline ring fission of coumarins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000174</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>K.</given-names></name>
<name><surname>Hanson</surname>
<given-names>M. J.</given-names></name>
<name><surname>Taylor</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>174</fpage>
<lpage>177</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000174">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000174">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Conformation and reactivity. Part VII. Kinetics of the alkaline hydrolysis of the methyl and ethyl &lt;i&gt;trans&lt;/i&gt;-decalincarboxylates, and 4-t-butylcyclohexanecarboxylates, certain &lt;i&gt;trans&lt;/i&gt;-4-substituted cyclohexanecarboxylates, and methyl and ethyl cyclohexanecarboxylate in alcohol–water and dioxan–water mixtures</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000178</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Ehsan</surname>
<given-names>A.</given-names></name>
<name><surname>Shorter</surname>
<given-names>J.</given-names></name>
<name><surname>Toyne</surname>
<given-names>K. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>178</fpage>
<lpage>184</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000178">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000178">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of lead tetra-acetate. Part XII. The oxidation of triphenyl-methanol and &lt;i&gt;p&lt;/i&gt;-anisyldiphenylmethanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000184</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Watson</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>184</fpage>
<lpage>190</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000184">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000184">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The mechanism of reduction of nitrosobenzene by alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000191</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hutton</surname>
<given-names>J.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>191</fpage>
<lpage>195</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000191">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000191">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Substituent effects in the electrophilic substitution of deactivated systems. Part I. The nitration of 4-alkylphenyltrimethylammonium ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000196</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Utley</surname>
<given-names>J. H. P.</given-names></name>
<name><surname>Vaughan</surname>
<given-names>T. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>196</fpage>
<lpage>198</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000196">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000196">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A stopped-flow investigation of the rate of formation and disappearance of the 4,4′,4″-trimethoxytriphenylcarbonium ion in dioxan–water mixtures</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000198</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nicholson</surname>
<given-names>H.</given-names></name>
<name><surname>Wyatt</surname>
<given-names>P. A. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>198</fpage>
<lpage>202</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000198">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000198">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electrophilic substitutions in metallocenes. Part I. The protodesilylation of trimethylsilylferrocene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000202</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marr</surname>
<given-names>G.</given-names></name>
<name><surname>Webster</surname>
<given-names>D. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>202</fpage>
<lpage>204</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000202">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000202">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reactions of &lt;i&gt;o&lt;/i&gt;-nitrobenzaldehydes with bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000205</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forbes</surname>
<given-names>E. J.</given-names></name>
<name><surname>Gregory</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>205</fpage>
<lpage>207</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000205">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000205">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The action of alkali on 2,4-dinitrobenzaldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000207</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forbes</surname>
<given-names>E. J.</given-names></name>
<name><surname>Gregory</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>207</fpage>
<lpage>209</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000207">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000207">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The &lt;i&gt;H&lt;/i&gt;&lt;sub&gt;0&lt;/sub&gt; acidity function in aqueous 2-butoxyethanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000209</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tillett</surname>
<given-names>J. G.</given-names></name>
<name><surname>Young</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>209</fpage>
<lpage>211</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000209">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000209">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Spectroscopic studies of some 1-phenylpyrazole derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000211</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Finar</surname>
<given-names>I. L.</given-names></name>
<name><surname>Rackham</surname>
<given-names>D. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>211</fpage>
<lpage>214</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000211">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000211">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetic studies of the fluorene series. Part VI. The reaction of 3-substituted fluorenones with sodium borohydride and the acidcatalysed solvolysis of 3-substituted 9-diazofluorenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000214</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harget</surname>
<given-names>A. J.</given-names></name>
<name><surname>Warren</surname>
<given-names>Keith D.</given-names></name>
<name><surname>Yandle</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>214</fpage>
<lpage>218</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000214">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000214">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The effect of halide ions on the decomposition of ethyl diazoacetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000219</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Albery</surname>
<given-names>W. J.</given-names></name>
<name><surname>Hutchins</surname>
<given-names>J. E. C.</given-names></name>
<name><surname>Hyde</surname>
<given-names>R. M.</given-names></name>
<name><surname>Johnson</surname>
<given-names>R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>219</fpage>
<lpage>224</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000219">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000219">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nuclear magnetic resonance studies of donor–acceptor interaction in boron halide complexes. Part VI. The relative donor strengths of nitrobenzene and pentafluoronitrobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000224</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mooney</surname>
<given-names>E. F.</given-names></name>
<name><surname>Qaseem</surname>
<given-names>M. A.</given-names></name>
<name><surname>Winson</surname>
<given-names>P. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>224</fpage>
<lpage>226</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000224">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000224">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance studies. Part XVI. Photochemical reactions of biacetyl with some benzenoid compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000227</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baum</surname>
<given-names>E. J.</given-names></name>
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>227</fpage>
<lpage>232</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000227">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000227">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The interaction of poly-2-vinylpyridine 1-oxide and poly-4-vinylpyridine 1-oxide with monosilicic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000233</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Holt</surname>
<given-names>P. F.</given-names></name>
<name><surname>Nasrallah</surname>
<given-names>E. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>233</fpage>
<lpage>237</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000233">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000233">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aromatic nucleophilic replacement. Part XIV. The mode of transmission of the inductive effect in the benzene ring and the relative activating power of the &lt;sup&gt;+&lt;/sup&gt;NMe&lt;sub&gt;2&lt;/sub&gt;O&lt;sup&gt;–&lt;/sup&gt;, &lt;sup&gt;+&lt;/sup&gt;NMe&lt;sub&gt;3&lt;/sub&gt;, and NO&lt;sub&gt;2&lt;/sub&gt; groups in aromatic nucleophilic replacement reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000238</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bevan</surname>
<given-names>C. W. L.</given-names></name>
<name><surname>Emokpae</surname>
<given-names>T. A.</given-names></name>
<name><surname>Hirst</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>238</fpage>
<lpage>241</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000238">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000238">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular conformations. Part V. The tricyclo[5,3,1,1&lt;sup&gt;2,6&lt;/sup&gt;]dodecane system: &lt;i&gt;X&lt;/i&gt;-ray analysis of 12-hydroxy-6-methyltricyclo[5,3,1,1&lt;sup&gt;2,6&lt;/sup&gt;]dodec-3-yl &lt;i&gt;p&lt;/i&gt;-iodobenzoate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000242</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Macrosson</surname>
<given-names>W. D. K.</given-names></name>
<name><surname>Ferguson</surname>
<given-names>George</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>242</fpage>
<lpage>250</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000242">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000242">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance of aliphatic nitroxides. Part II. The cyclic radicals from pyrrolidine, piperidine, morpholine, and hexamethyleneimine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000251</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hudson</surname>
<given-names>A.</given-names></name>
<name><surname>Hussain</surname>
<given-names>H. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>251</fpage>
<lpage>253</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000251">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000251">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron impact-induced eliminations of acetaldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000254</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rix</surname>
<given-names>M. J.</given-names></name>
<name><surname>Webster</surname>
<given-names>B. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>254</fpage>
<lpage>258</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000254">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000254">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The mass spectra of benzocycloalkenones and their enol acetates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000258</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Boocock</surname>
<given-names>D. G. B.</given-names></name>
<name><surname>Waight</surname>
<given-names>E. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>258</fpage>
<lpage>261</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000258">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000258">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Benzene-induced solvent shifts in nuclear magnetic resonance spectroscopy</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000261</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baker</surname>
<given-names>K. M.</given-names></name>
<name><surname>Davis</surname>
<given-names>B. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>261</fpage>
<lpage>263</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000261">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000261">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photolysis of biacetyl in the presence of triethylborine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000264</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Grotewold</surname>
<given-names>J.</given-names></name>
<name><surname>Lissi</surname>
<given-names>E. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>264</fpage>
<lpage>267</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000264">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000264">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The hydrolysis of some norbornyl sulphites and related compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000267</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Manser</surname>
<given-names>G. E.</given-names></name>
<name><surname>Mesure</surname>
<given-names>A. D.</given-names></name>
<name><surname>Tillett</surname>
<given-names>J. G.</given-names></name>
<name><surname>Young</surname>
<given-names>R. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>267</fpage>
<lpage>269</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000267">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000267">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amine oxidation. Part I. The oxidation of &lt;i&gt;NN&lt;/i&gt;-dimethylaniline to crystal violet and methyl violet</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000269</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Smith</surname>
<given-names>J. R. Lindsay</given-names></name>
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Walker</surname>
<given-names>W. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>269</fpage>
<lpage>274</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000269">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000269">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Protonation equilibria of amides and related compounds. Part II. Butyramide, &lt;i&gt;N&lt;/i&gt;-butyrylglycine, and some carbamic acid esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000275</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armstrong</surname>
<given-names>V. C.</given-names></name>
<name><surname>Moodie</surname>
<given-names>R. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>275</fpage>
<lpage>277</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000275">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000275">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The ultraviolet spectra of nitrophenylhydrazones in neutral solution; substituent and solvent effects</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000277</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rappoport</surname>
<given-names>Zvi</given-names></name>
<name><surname>Sheradsky</surname>
<given-names>Tuvia</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>277</fpage>
<lpage>291</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000277">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000277">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Separation of diastereoisomers by gas–liquid chromatography : esters of butane-2,3-diol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000291</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nurok</surname>
<given-names>D.</given-names></name>
<name><surname>Taylor</surname>
<given-names>G. L.</given-names></name>
<name><surname>Stephen</surname>
<given-names>A. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>291</fpage>
<lpage>294</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000291">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000291">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron capture by chlorinated biphenyls</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000295</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gregory</surname>
<given-names>N. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>295</fpage>
<lpage>300</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000295">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000295">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unusual pyridone salts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000300</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thyagarajan</surname>
<given-names>B. S.</given-names></name>
<name><surname>Rajagopalan</surname>
<given-names>K.</given-names></name>
<name><surname>Gopalakrishnan</surname>
<given-names>P. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>300</fpage>
<lpage>303</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000300">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000300">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mass spectra of isomers. Part I. Cyclobutanes and cyclohexenes of molecular formula C&lt;sub&gt;10&lt;/sub&gt;H&lt;sub&gt;16&lt;/sub&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000304</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brittain</surname>
<given-names>E. F. H.</given-names></name>
<name><surname>Wells</surname>
<given-names>C. H. J.</given-names></name>
<name><surname>Paisley</surname>
<given-names>H. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>304</fpage>
<lpage>307</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000304">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000304">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Fluorine nuclear magnetic resonance spectra of some polyfluoroaromatic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000308</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fields</surname>
<given-names>R.</given-names></name>
<name><surname>Lee</surname>
<given-names>J.</given-names></name>
<name><surname>Mowthorpe</surname>
<given-names>D. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>308</fpage>
<lpage>312</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000308">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000308">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heteroaromatic reactivity. Part III. The kinetics of nitration of cinnoline and 2-methylcinnolinium perchlorate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000312</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Moodie</surname>
<given-names>R. B.</given-names></name>
<name><surname>Qureshi</surname>
<given-names>E. A.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
<name><surname>Gleghorn</surname>
<given-names>J. T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>312</fpage>
<lpage>315</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000312">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000312">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Heteroaromatic reactivity. Part IV. The kinetics of nitration of cinnoline 2-oxide and quinoline 1-oxide in sulphuric acid. The mechanism of nitration of &lt;i&gt;N&lt;/i&gt;-heteroaromatic oxides, with special reference to 2,6-lutidine 1-oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000316</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gleghorn</surname>
<given-names>J. T.</given-names></name>
<name><surname>Moodie</surname>
<given-names>R. B.</given-names></name>
<name><surname>Qureshi</surname>
<given-names>E. A.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>316</fpage>
<lpage>323</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000316">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000316">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polar and steric effects in hydrogen abstraction by dialkylamine cation radicals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000324</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bernardi</surname>
<given-names>R.</given-names></name>
<name><surname>Galli</surname>
<given-names>R.</given-names></name>
<name><surname>Minisci</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>324</fpage>
<lpage>325</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000324">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000324">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Spectroscopic studies. Part III. Proton magnetic resonance spectra and solvent shifts of some αβ-unsaturated ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000326</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cottee</surname>
<given-names>F. H.</given-names></name>
<name><surname>Timmons</surname>
<given-names>C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>326</fpage>
<lpage>330</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000326">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000326">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quantitative aspects of Lewis acidity. Part XII. Equilibria between aluminium chloride and substituted anilines in ether solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000331</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mohammad</surname>
<given-names>Ali</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>331</fpage>
<lpage>331</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000331">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000331">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The thermal decomposition of alkyl vinyl ethers. Part II. The inhibited decompositions of t-butyl, isopropyl, and 2-chloroethyl vinyl ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000332</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bamkole</surname>
<given-names>T. O.</given-names></name>
<name><surname>Emovon</surname>
<given-names>E. U.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>332</fpage>
<lpage>333</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000332">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000332">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Preparation and study of some 5- and 7-substituted 4-nitrobenzofurazans and their &lt;i&gt;N&lt;/i&gt;-oxides; a retro-Boulton–Katritzky rearrangement</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000334</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ghosh</surname>
<given-names>P. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>334</fpage>
<lpage>338</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000334">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000334">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An infrared study of competitive intramolecular hydrogen bonding in a series of benzyl alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000338</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>I. D.</given-names></name>
<name><surname>Eglinton</surname>
<given-names>G.</given-names></name>
<name><surname>Raphael</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>338</fpage>
<lpage>343</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000338">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000338">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics and mechanism of the reaction between nitrous acid and hydroxylamine. Part II. The alkyl hydroxylamines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000344</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Morgan</surname>
<given-names>T. D. B.</given-names></name>
<name><surname>Stedman</surname>
<given-names>G.</given-names></name>
<name><surname>Hughes</surname>
<given-names>M. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>344</fpage>
<lpage>349</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000344">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000344">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The analysis of mixtures of the n-octenes, octalins, t-butylcyclohexenes, octanols, decalols, and t-butylcyclohexanols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000349</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>N. C. G.</given-names></name>
<name><surname>Clarke</surname>
<given-names>J. R. P.</given-names></name>
<name><surname>Hill</surname>
<given-names>R. R.</given-names></name>
<name><surname>Oberhänsli</surname>
<given-names>P.</given-names></name>
<name><surname>Parish</surname>
<given-names>J. H.</given-names></name>
<name><surname>Southam</surname>
<given-names>R. M.</given-names></name>
<name><surname>Whiting</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>349</fpage>
<lpage>354</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000349">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000349">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Classical carbonium ions. Part I. The solvolysis of some typical secondary arenesulphonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000355</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Campbell</surname>
<given-names>N. C. G.</given-names></name>
<name><surname>Muir</surname>
<given-names>D. M.</given-names></name>
<name><surname>Hill</surname>
<given-names>R. R.</given-names></name>
<name><surname>Parish</surname>
<given-names>J. H.</given-names></name>
<name><surname>Southam</surname>
<given-names>R. M.</given-names></name>
<name><surname>Whiting</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>355</fpage>
<lpage>364</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000355">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000355">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereochemical studies. Part XLVI. The 2-alkylcyclohexyl tosylate solvolysis problem: the solvolysis of the 2-methyl-4-t-butylcyclohexyl tosylates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000365</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pánková</surname>
<given-names>M.</given-names></name>
<name><surname>Sicher</surname>
<given-names>J.</given-names></name>
<name><surname>Tichý</surname>
<given-names>M.</given-names></name>
<name><surname>Whiting</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>365</fpage>
<lpage>370</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000365">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000365">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aromatic reactivity. Part XXXVI. Detritiation of some 5-substituted 2-tritiothiophens</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000370</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Butler</surname>
<given-names>A. R.</given-names></name>
<name><surname>Eaborn</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>370</fpage>
<lpage>372</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000370">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000370">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Topochemistry. Part XXVIII. The system: 4-chloro-&lt;i&gt;N&lt;/i&gt;-salicylideneaniline—4-bromo-&lt;i&gt;N&lt;/i&gt;-salicylideneaniline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000373</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cohen</surname>
<given-names>M. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>373</fpage>
<lpage>376</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000373">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000373">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The crystal and molecular structure of saccharin (&lt;i&gt;o&lt;/i&gt;-sulphobenzoic imide)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000376</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bart</surname>
<given-names>J. C. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>376</fpage>
<lpage>382</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000376">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000376">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nuclear magnetic resonance spectra of 2,7-dioxabicyclo[2,2,1]heptanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000382</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gaoni</surname>
<given-names>Y.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>382</fpage>
<lpage>386</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000382">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000382">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Symmetry of carboxylate ions. Infrared spectra of &lt;sup&gt;18&lt;/sup&gt;O labelled sodium deuterioformate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000389</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Junge</surname>
<given-names>H.</given-names></name>
<name><surname>Musso</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>389</fpage>
<lpage>391</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000389">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000389">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electrophilic substitution in five-membered heterocyclic systems. Part VI. Kinetics of the bromination of the 2-methoxycarbonyl derivatives of furan, thiophen, and pyrrole in acetic acid solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000392</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Linda</surname>
<given-names>Paolo</given-names></name>
<name><surname>Marino</surname>
<given-names>Gianlorenzo</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>392</fpage>
<lpage>394</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000392">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000392">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nuclear magnetic resonance evidence for micelle formation in solutions of sodium 4,4-dimethyl-4-silapentane-1-sulphonate containing paramagnetic ions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000395</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Donaldson</surname>
<given-names>B. R.</given-names></name>
<name><surname>Schwarz</surname>
<given-names>J. C. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>395</fpage>
<lpage>397</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000395">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000395">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Products, kinetics, and mechanism of the chlorination of 2,3-dimethylbenzothiophen in acetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000397</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baciocchi</surname>
<given-names>Enrico</given-names></name>
<name><surname>Mandolini</surname>
<given-names>Luigi</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>397</fpage>
<lpage>400</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000397">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000397">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Side-chain reactivity of indole derivatives. The reaction of 3-indolylmethyltrimethylammonium methyl sulphate with sodium toluene-&lt;i&gt;p&lt;/i&gt;-thiolate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000401</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baciocchi</surname>
<given-names>Enrico</given-names></name>
<name><surname>Schiroli</surname>
<given-names>Alberto</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>401</fpage>
<lpage>403</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000401">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000401">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of the uncatalysed transesterification of malonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000404</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rowland</surname>
<given-names>S. P.</given-names></name>
<name><surname>Pearcy</surname>
<given-names>L. Z.</given-names></name>
<name><surname>Mack</surname>
<given-names>C. H.</given-names></name>
<name><surname>Janssen</surname>
<given-names>H. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>404</fpage>
<lpage>406</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000404">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000404">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Quinazolines. Part XI. Kinetics of methoxy-dehalogenation in 5-, 6-, 7-, and 8-substituted quinazolines in methanol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000407</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armarego</surname>
<given-names>W. L. F.</given-names></name>
<name><surname>Smith</surname>
<given-names>J. I. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>407</fpage>
<lpage>407</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000407">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000407">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The electron spin resonance spectra of some hydroxylamine free radicals. Part IV. Radicals from alkylhydroximic acids and amidoximes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000408</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Millen</surname>
<given-names>(Miss) M. H.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>408</fpage>
<lpage>411</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000408">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000408">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Long range interactions. Part I. Enhanced kinetic acidity of bicyclo-[3,2,1]octa-2,6-diene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000411</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>J. M.</given-names></name>
<name><surname>Occolowitz</surname>
<given-names>J. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>411</fpage>
<lpage>418</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000411">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000411">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A kinetic study of the gas-phase thermal decomposition of 1,1-dimethyl-1-silacyclobutane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000419</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flowers</surname>
<given-names>M. C.</given-names></name>
<name><surname>Gusel'nikov</surname>
<given-names>L. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>419</fpage>
<lpage>423</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000419">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000419">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hybridisation in norbornane and some derivatives by the method of maximum overlap</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000423</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Randić</surname>
<given-names>M.</given-names></name>
<name><surname>Stefanović</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>423</fpage>
<lpage>425</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000423">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000423">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Radiolysis and photolysis of diphenyl carbonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000425</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davis</surname>
<given-names>A.</given-names></name>
<name><surname>Golden</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>425</fpage>
<lpage>427</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000425">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000425">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unstable intermediates. Part LI. An electron spin resonance study of radicals and radical pairs formed by irradiation of organic carbonates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000428</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McRae</surname>
<given-names>J. A.</given-names></name>
<name><surname>Symons</surname>
<given-names>M. C. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>428</fpage>
<lpage>430</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000428">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000428">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Intermediates in the decomposition of aliphatic diazo-compounds. Part V. The effects of hydroxylic compounds on the decomposition of 4,4′-dichlorodiphenyldiazomethane catalysed by perchloric and toluene-&lt;i&gt;p&lt;/i&gt;-sulphonic acids in acetonitrile</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000430</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bethell</surname>
<given-names>D.</given-names></name>
<name><surname>Howard</surname>
<given-names>R. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>430</fpage>
<lpage>434</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000430">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000430">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;sup&gt;1&lt;/sup&gt;H nuclear magnetic resonance spectra of some squaramides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000435</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thorpe</surname>
<given-names>J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>435</fpage>
<lpage>436</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000435">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000435">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in decarboxylation. Part VI. A comparison of the transition states for the decarboxylation of β-keto- and βγ-unsaturated acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000436</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bigley</surname>
<given-names>D. B.</given-names></name>
<name><surname>Thurman</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>436</fpage>
<lpage>440</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000436">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000436">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereochemical studies. Part XLVII. Conformational analysis of many-membered ring compounds. The cyclododecenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000441</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sicher</surname>
<given-names>J.</given-names></name>
<name><surname>Svoboda</surname>
<given-names>M.</given-names></name>
<name><surname>Mallon</surname>
<given-names>Barbara J.</given-names></name>
<name><surname>Turner</surname>
<given-names>R. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>441</fpage>
<lpage>447</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000441">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000441">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photolysis of acetyl chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000447</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Capey</surname>
<given-names>W. D.</given-names></name>
<name><surname>Majer</surname>
<given-names>J. R.</given-names></name>
<name><surname>Robb</surname>
<given-names>J. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>447</fpage>
<lpage>449</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000447">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000447">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The solvolysis of 2-trimethylsilylpyridine by alcohols and by water</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000450</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>D. G.</given-names></name>
<name><surname>Bradney</surname>
<given-names>M. A. M.</given-names></name>
<name><surname>Webster</surname>
<given-names>D. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>450</fpage>
<lpage>452</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000450">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000450">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carbanions. Part III. Pyramidal structure of α-sulphonyl carbanions in the norbornene system. Comparison with α-methoxycarbonyl carbanions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000453</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Maccagnani</surname>
<given-names>G.</given-names></name>
<name><surname>Montanari</surname>
<given-names>F.</given-names></name>
<name><surname>Taddei</surname>
<given-names>F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>453</fpage>
<lpage>458</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000453">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000453">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Some observations relating to substituent effects in halogenation. Part III. The kinetics of the reaction of diphenylmethane with chlorine acetate in aqueous acetic acid at 25°</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000459</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hassan</surname>
<given-names>M.</given-names></name>
<name><surname>Yousif</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>459</fpage>
<lpage>462</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000459">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000459">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Generation of nitrenes from alkanamidates and alkanesulphonamidates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000463</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Robson</surname>
<given-names>P.</given-names></name>
<name><surname>Speakman</surname>
<given-names>P. R. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>463</fpage>
<lpage>467</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000463">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000463">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The crystal and molecular structure of phenanthrenechromium tricarbonyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000467</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Muir</surname>
<given-names>K. W.</given-names></name>
<name><surname>Ferguson</surname>
<given-names>G.</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>467</fpage>
<lpage>476</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000467">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000467">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The crystal and molecular structure of 9,10-dihydrophenanthrene-chromium tricarbonyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000476</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Muir</surname>
<given-names>K. W.</given-names></name>
<name><surname>Ferguson</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>476</fpage>
<lpage>485</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000476">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000476">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An electron spin resonance study of the free radicals induced in &lt;i&gt;O&lt;/i&gt;-methylisouronium chloride by &lt;i&gt;X&lt;/i&gt;-irradiation at 77°K</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000485</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cadena jun. </surname>
<given-names>D. G.</given-names></name>
<name><surname>Rowlands</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>485</fpage>
<lpage>488</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000485">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000485">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An electron spin resonance investigation of &lt;i&gt;X&lt;/i&gt;-irradiated DL-methionine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000488</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cadena jun. </surname>
<given-names>D. G.</given-names></name>
<name><surname>Rowlands</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>488</fpage>
<lpage>491</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000488">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000488">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aromatic substitution. Part XVIII. Kinetics of reactions between some halogeno-pyridines and -picolines and their &lt;i&gt;N&lt;/i&gt;-oxides with methoxide ion in methanol and in dimethyl sulphoxide. Effect of alkyl groups on rates on orientation in nucleophilic aromatic substitution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000492</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abramovitch</surname>
<given-names>R. A.</given-names></name>
<name><surname>Helmer</surname>
<given-names>F.</given-names></name>
<name><surname>Liveris</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>492</fpage>
<lpage>496</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000492">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000492">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aromatic substitution. Part XIX. Arylation of aromatic compounds with benzenediazonium tetrafluoroborate in homogeneous solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000497</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abramovitch</surname>
<given-names>R. A.</given-names></name>
<name><surname>Gadallah</surname>
<given-names>F. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>497</fpage>
<lpage>500</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000497">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000497">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of the reactions of olefins with halogens in aqueous solution. Part III. Reaction of bromine with acrylic acid, crotonic acid, and ethyl acrylate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000500</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bell</surname>
<given-names>R. P.</given-names></name>
<name><surname>Dolman</surname>
<given-names>Douglas</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>500</fpage>
<lpage>503</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000500">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000500">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular polarisability. The dipole moments and Molar Kerr constants of the dinitrobenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000503</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Calderbank</surname>
<given-names>K. E.</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Ritchie</surname>
<given-names>G. L. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>503</fpage>
<lpage>506</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000503">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000503">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular polarisability. The Molar Kerr constants of aniline and of three substituted anilines in a variety of non-polar media</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000507</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aroney</surname>
<given-names>M. J.</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Radom</surname>
<given-names>L.</given-names></name>
<name><surname>Ritchie</surname>
<given-names>G. L. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>507</fpage>
<lpage>512</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000507">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000507">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics and mechanism of the gas-phase reaction of the CIO radical with alkanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000513</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shaw</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>513</fpage>
<lpage>514</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000513">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000513">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The acetate-catalysed hydrolysis of aryl acetates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000515</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
<name><surname>Oakenfull</surname>
<given-names>D. G.</given-names></name>
<name><surname>Riley</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>515</fpage>
<lpage>519</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000515">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000515">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reduction of 9,10-anthraquinones. Part II. Polarography of 2-hydroxy-9,10-anthrahydroquinones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000519</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Broadbent</surname>
<given-names>A. D.</given-names></name>
<name><surname>Sommermann</surname>
<given-names>E. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>519</fpage>
<lpage>522</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000519">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000519">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in mass spectrometry. Part XXVIII. Hydrogen scrambling between phenyl rings of diphenylmethanol and diphenylmethyl chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000522</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
<name><surname>Ward</surname>
<given-names>Robert S.</given-names></name>
<name><surname>Cooks</surname>
<given-names>R. Graham</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>522</fpage>
<lpage>525</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000522">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000522">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aromatic detritiation. Part III. Deviations from additivity in detritiation of xylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000526</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ansell</surname>
<given-names>H. V.</given-names></name>
<name><surname>Taylor</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>526</fpage>
<lpage>528</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000526">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000526">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Substituent effects of positive poles in aromatic substitution. Part III. Nature of the deactivating effect of the trimethylammonio-group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000528</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Modro</surname>
<given-names>T. A.</given-names></name>
<name><surname>Ridd</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>528</fpage>
<lpage>534</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000528">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000528">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Substituent effects of positive poles in aromatic substitution. Part IV. The effects of the nitrogen, phosphorus, arsenic, and antimony poles on the orientation and rate of nitration</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000534</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gastaminza</surname>
<given-names>Alicia</given-names></name>
<name><surname>Modro</surname>
<given-names>T. A.</given-names></name>
<name><surname>Ridd</surname>
<given-names>J. H.</given-names></name>
<name><surname>Utley</surname>
<given-names>J. H. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>534</fpage>
<lpage>539</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000534">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000534">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Evidence for a planar intermediate in alkaline solvolysis of methyl &lt;i&gt;N&lt;/i&gt;-cyclohexylphosphoramidothioic chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000539</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gerrard</surname>
<given-names>A. F.</given-names></name>
<name><surname>Hamer</surname>
<given-names>N. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>539</fpage>
<lpage>543</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000539">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000539">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Conformational effects in the hydrolysis of cyclic acetals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000543</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Watts</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>543</fpage>
<lpage>545</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000543">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000543">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Arrhenius parameters for the alkaline hydrolysis of esters in aqueous solution. Part II. Acetylcholine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000545</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wright</surname>
<given-names>(Mrs.) Margaret Robson</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>545</fpage>
<lpage>547</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000545">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000545">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Arrhenius parameters for the alkaline hydrolysis of esters in aqueous solution. Part III. Methyl betaine methyl ester</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000548</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wright</surname>
<given-names>(Mrs.) Margaret Robson</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>548</fpage>
<lpage>550</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000548">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000548">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Steric requirements of &lt;i&gt;sp&lt;/i&gt;&lt;sup&gt;2&lt;/sup&gt;-hybridised lone electron pairs. Part I. The conformations of 2-(pyridylmethylene)indan-1-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000550</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bobbitt</surname>
<given-names>J. M.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Kennewell</surname>
<given-names>P. D.</given-names></name>
<name><surname>Snarey</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>550</fpage>
<lpage>554</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000550">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000550">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Steric requirements of &lt;i&gt;sp&lt;/i&gt;&lt;sup&gt;2&lt;/sup&gt;-hybridised lone electron pairs. Part II. The conformations of 2-(pyridylmethylene)-benzofuran-3(2&lt;i&gt;H&lt;/i&gt;)-ones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000554</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Kennewell</surname>
<given-names>P. D.</given-names></name>
<name><surname>Snarey</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>554</fpage>
<lpage>556</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000554">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000554">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tautomeric pyridines. Part X. Effects of substituents on pyridone–hydroxypyridine equilibria and pyridone basicity</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000556</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gordon</surname>
<given-names>A.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Roy</surname>
<given-names>S. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>556</fpage>
<lpage>561</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000556">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000556">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular polarisability. The effect of &lt;i&gt;para&lt;/i&gt;-substituents in aniline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000561</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aroney</surname>
<given-names>M. J.</given-names></name>
<name><surname>Calderbank</surname>
<given-names>K. E.</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Pierens</surname>
<given-names>R. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>561</fpage>
<lpage>565</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000561">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000561">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation. Part XXIV. The cyanide catalysed hydrolysis of esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000565</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hibbert</surname>
<given-names>F.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>565</fpage>
<lpage>568</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000565">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000565">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation. Part XXV. Reactions of acyl cyanides. The spontaneous and catalysed benzoylation of butylamine in ether solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000568</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hibbert</surname>
<given-names>F.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>568</fpage>
<lpage>573</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000568">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000568">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Equilibria between carboxylic acids and n-butylamine in diethyl ether solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000573</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hibbert</surname>
<given-names>F.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. N. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>573</fpage>
<lpage>575</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000573">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000573">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on the successive anodic methoxylation of some ring-substituted phenylacetic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000576</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wladislaw</surname>
<given-names>B.</given-names></name>
<name><surname>Viertler</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>576</fpage>
<lpage>579</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000576">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000576">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of the hydrolysis in 1 : 3 water–acetone of aliphatic esters having substituents in the alkyl group, catalysed by an acid resin or an acidic solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000579</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Affrossman</surname>
<given-names>S.</given-names></name>
<name><surname>Murray</surname>
<given-names>J. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>579</fpage>
<lpage>582</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000579">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000579">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The Molar Kerr constants and anisotropic polarisabilities of certain sterically hindered aromatic nitro-compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000582</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Huang</surname>
<given-names>H. H.</given-names></name>
<name><surname>Ng</surname>
<given-names>S. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>582</fpage>
<lpage>587</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000582">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000582">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The acid dissociation constants of substituted (phenylthio)acetic and (phenylseleno)acetic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000588</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pettit</surname>
<given-names>L. D.</given-names></name>
<name><surname>Royston</surname>
<given-names>A.</given-names></name>
<name><surname>Sherrington</surname>
<given-names>C.</given-names></name>
<name><surname>Whewell</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>588</fpage>
<lpage>590</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000588">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000588">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance studies. Part XVII. Reactions of some free radicals with nitroalkanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000590</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McMillan</surname>
<given-names>Miss M.</given-names></name>
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>590</fpage>
<lpage>597</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000590">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000590">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics and mechanism of the reaction between nitrous acid and hydroxylamine. Part III. The formation of hyponitrous acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000597</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hussain</surname>
<given-names>M. A.</given-names></name>
<name><surname>Stedman</surname>
<given-names>G.</given-names></name>
<name><surname>Hughes</surname>
<given-names>M. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>597</fpage>
<lpage>603</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000597">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000597">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism of benzidine and semidine rearrangements. Part XVII. Kinetics and products of the acid rearrangements of 2,2′-dimethoxy- and 4-methoxy-hydrazobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000605</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banthorpe</surname>
<given-names>D. V.</given-names></name>
<name><surname>Cooper</surname>
<given-names>Anthony</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>605</fpage>
<lpage>609</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000605">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000605">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism of benzidine and semidine rearrangements. Part XVIII. Kinetics and products of the acid conversion of 4-acetamidohydrazobenzene, products from 4-aminohydrazobenzene, normality of &lt;i&gt;p&lt;/i&gt;-semidine formation, and crossed redox analogues of disproportionation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000609</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banthorpe</surname>
<given-names>D. V.</given-names></name>
<name><surname>Cooper</surname>
<given-names>Anthony</given-names></name>
<name><surname>Ingold</surname>
<given-names>C. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>609</fpage>
<lpage>614</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000609">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000609">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism of benzidine and semidine rearrangements. Part XIX. Kinetics and products of the acid conversion of 2,2′-difluorohydrazobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000615</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banthorpe</surname>
<given-names>D. V.</given-names></name>
<name><surname>O'Sullivan</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>615</fpage>
<lpage>617</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000615">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000615">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism of benzidine and semidine rearrangements. Part XX. Kinetics and products of the acid conversions of 2,2′-dichloro-,4-chloro-, and 4,4′-dichloro-hydrazobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000618</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banthorpe</surname>
<given-names>D. V.</given-names></name>
<name><surname>Cooper</surname>
<given-names>Anthony</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>618</fpage>
<lpage>623</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000618">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000618">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism of benzidine and semidine rearrangements. Part XXI. Kinetics and products of the acid conversion of 2,2′-dibromo- and of 4,4′-dibromo-hydrazobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000624</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banthorpe</surname>
<given-names>D. V.</given-names></name>
<name><surname>Ingold</surname>
<given-names>C. K.</given-names></name>
<name><surname>O'Sullivan</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>624</fpage>
<lpage>627</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000624">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000624">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism of benzidine and semidine rearrangements. Part XXII. Kinetics and products of the acid conversion of 2,2′-di-iodo- and 4,4′-di-iodo-hydrazobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000627</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banthorpe</surname>
<given-names>D. V.</given-names></name>
<name><surname>O'Sullivan</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>627</fpage>
<lpage>630</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000627">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000627">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The separation of polar and steric effects. Part VIII. The influence of the solvent on the kinetics of the reactions of benzoic acid and &lt;i&gt;meta&lt;/i&gt;- or &lt;i&gt;para&lt;/i&gt;-substituted benzoic acid with diazodiphenylmethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000631</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Buckley</surname>
<given-names>A.</given-names></name>
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Dack</surname>
<given-names>M. R. J.</given-names></name>
<name><surname>Shorter</surname>
<given-names>J.</given-names></name>
<name><surname>Wall</surname>
<given-names>H. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>631</fpage>
<lpage>638</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000631">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000631">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanistic studies in strongly basic media. Part VI. The kinetics of base-induced hydrogen-isotope exchange and autoxidation of fluorene in t-butyl alcohol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000638</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bethell</surname>
<given-names>D.</given-names></name>
<name><surname>Talbot</surname>
<given-names>R. J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>638</fpage>
<lpage>642</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000638">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000638">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies of kinetic acidity dependence in certain oxidation reactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000642</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mehrotra</surname>
<given-names>Raj Narain</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>642</fpage>
<lpage>644</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000642">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000642">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The electric dipole moments of chloro-anilines and of some chloro-, bromo-, and nitro-substituted amino-pyridines in benzene and 1,4-dioxan solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000645</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cumper</surname>
<given-names>C. W. N.</given-names></name>
<name><surname>Singleton</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>645</fpage>
<lpage>649</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000645">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000645">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The ultraviolet spectra of aniline, 2-, 3-, and 4-aminopyridines and of some of their derivatives in n-hexane, 1,4-dioxan, ethanol, and water solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000649</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cumper</surname>
<given-names>C. W. N.</given-names></name>
<name><surname>Singleton</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>649</fpage>
<lpage>651</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000649">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000649">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The &lt;i&gt;X&lt;/i&gt;-ray analyses of acutumine and its acetate; a trial of a short cut in the structure elucidation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000652</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Nishikawa</surname>
<given-names>Masao</given-names></name>
<name><surname>Kamiya</surname>
<given-names>Kazuhide</given-names></name>
<name><surname>Tomita</surname>
<given-names>Masao</given-names></name>
<name><surname>Okamoto</surname>
<given-names>Yasuko</given-names></name>
<name><surname>Kikuchi</surname>
<given-names>Tohru</given-names></name>
<name><surname>Osaki</surname>
<given-names>Kenji</given-names></name>
<name><surname>Tomiie</surname>
<given-names>(the late) Yujiro</given-names></name>
<name><surname>Nitta</surname>
<given-names>Isamu</given-names></name>
<name><surname>Goto</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>652</fpage>
<lpage>658</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000652">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000652">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The mass spectrometry of nitrate esters and related compounds. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000659</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fraser</surname>
<given-names>R. T. M.</given-names></name>
<name><surname>Paul</surname>
<given-names>N. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>659</fpage>
<lpage>663</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000659">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000659">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Factors in the formation of isomerically and optically pure alkyl halides. Part V. Conditions which determine the formation of 2-halogeno-2-methyl- and 2-halogeno-3-methyl-butanes in the preparation of 1-halogeno-2,2-dimethylpropanes from 2,2-dimethylpropan-1-ol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000664</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hudson</surname>
<given-names>H. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>664</fpage>
<lpage>667</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000664">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000664">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The structure of the 1 : 2 adduct of indene and dimethyl acetylenedicarboxylate: &lt;i&gt;X&lt;/i&gt;-ray analysis of a dibromo-derivative</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000667</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Muir</surname>
<given-names>K. W.</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>667</fpage>
<lpage>673</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000667">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000667">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitrogen-14 chemical shifts in ureas</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000673</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hampson</surname>
<given-names>P.</given-names></name>
<name><surname>Mathias</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>673</fpage>
<lpage>675</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000673">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000673">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The rate of reaction of some substituted anilines with phenyl isothiocyanate, and the correlation with amino-proton chemical shifts</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000676</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Akiyama</surname>
<given-names>H.</given-names></name>
<name><surname>Yoshida</surname>
<given-names>N.</given-names></name>
<name><surname>Araki</surname>
<given-names>Y.</given-names></name>
<name><surname>Ouchi</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>676</fpage>
<lpage>680</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000676">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000676">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reaction of some diazoamino-compounds with lead tetra-acetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000680</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Camaggi</surname>
<given-names>C. M.</given-names></name>
<name><surname>Tiecco</surname>
<given-names>M.</given-names></name>
<name><surname>Tundo</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>680</fpage>
<lpage>683</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000680">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000680">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nuclear magnetic resonance studies of six-membered rings. Part I. Rings inversion in heterocyclic compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000684</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Harris</surname>
<given-names>R. K.</given-names></name>
<name><surname>Spragg</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>684</fpage>
<lpage>691</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000684">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000684">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of lead tetra-acetate. Part XIII. Homolytic and heterolytic mechanisms in the oxidation of alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000692</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Watson</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>692</fpage>
<lpage>696</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000692">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000692">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conformation of hexamethylcyclohexane-1,3,5-trione as a solute in benzene or carbon tetrachloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000697</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>697</fpage>
<lpage>698</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000697">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000697">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The infrared &lt;sup&gt;1&lt;/sup&gt;H nuclear magnetic resonance, and ultraviolet spectra of some nuclear substituted styryl ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000698</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dimmock</surname>
<given-names>J. R.</given-names></name>
<name><surname>Carter</surname>
<given-names>P. L.</given-names></name>
<name><surname>Ralph</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>698</fpage>
<lpage>703</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000698">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000698">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of the addition of anilines to methyl vinyl ketone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000703</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ogata</surname>
<given-names>Y.</given-names></name>
<name><surname>Kawasaki</surname>
<given-names>A.</given-names></name>
<name><surname>Kishi</surname>
<given-names>I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>703</fpage>
<lpage>708</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000703">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000703">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic reactivity of organophosphorus compounds. Part I. The reaction of phosphonic and thiophosphonic acids with diethylmethyl-keten ketal</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000708</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hall</surname>
<given-names>C. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>708</fpage>
<lpage>711</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000708">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000708">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sulphuryl chloride as an electrophile. Part II. Substituted &lt;i&gt;m&lt;/i&gt;-di-methoxybenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000712</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bolton</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>712</fpage>
<lpage>713</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000712">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000712">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Sulphuryl chloride as an electrophile. Part III. Reactions with alkylbenzenes in nitromethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000714</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bolton</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>714</fpage>
<lpage>717</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000714">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000714">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Exchange of chlorine atoms during the reaction of hypochlorous acid with 2,3-dichloropropene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000718</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hopwood</surname>
<given-names>J. A.</given-names></name>
<name><surname>Williams</surname>
<given-names>D. L. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>718</fpage>
<lpage>721</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000718">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000718">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Proton chemical shifts of some halogenated steroids and t-butylcyclohexanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000721</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lack</surname>
<given-names>Ruth E.</given-names></name>
<name><surname>Ridley</surname>
<given-names>Anne B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>721</fpage>
<lpage>725</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000721">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000721">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular orbital calculations of pyrazoles. Part I. Alkyl- and arylpyrazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000725</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Finar</surname>
<given-names>I. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>725</fpage>
<lpage>732</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000725">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000725">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Fulvenes and thermochromic ethylenes. Part XLVIII. The mass spectra of some fulvenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000732</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lifshitz</surname>
<given-names>Chava</given-names></name>
<name><surname>Bergmann</surname>
<given-names>Ernst D.</given-names></name>
<name><surname>Rabinovitz</surname>
<given-names>Mordecai</given-names></name>
<name><surname>Agranat</surname>
<given-names>Israel</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>732</fpage>
<lpage>738</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000732">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000732">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Iodination and iodo-compounds. Part II. The kinetics of aromatic iodination by means of the tri-iodine cation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000739</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Arotsky</surname>
<given-names>J.</given-names></name>
<name><surname>Darby</surname>
<given-names>A. C.</given-names></name>
<name><surname>Hamilton</surname>
<given-names>J. B. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>739</fpage>
<lpage>742</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000739">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000739">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation and alkylation reactions. Part I. The cleavage of benzyl phenyl ethers by aluminium chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000742</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Palmer</surname>
<given-names>M. H.</given-names></name>
<name><surname>McVie</surname>
<given-names>G. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>742</fpage>
<lpage>744</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000742">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000742">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Alkylation and acylation reactions. Part II. The interaction of aryloxyacetyl chlorides with aluminium chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000745</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Palmer</surname>
<given-names>M. H.</given-names></name>
<name><surname>McVie</surname>
<given-names>G. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>745</fpage>
<lpage>751</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000745">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000745">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The &lt;i&gt;I&lt;/i&gt;&lt;sub&gt;&lt;i&gt;π&lt;/i&gt;&lt;/sub&gt; effect. Part II. Hammett relationships</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000751</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Godfrey</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>751</fpage>
<lpage>756</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000751">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000751">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Vapour spectrum of benzoxazole in the near ultraviolet</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000756</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lonardo</surname>
<given-names>G. Di</given-names></name>
<name><surname>Trombetti</surname>
<given-names>A.</given-names></name>
<name><surname>Zauli</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>756</fpage>
<lpage>759</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000756">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000756">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nuclear magnetic resonance study of tricrotonylidenetetramine (1,2,3,3a,4,5,6,6a,7,8,9,9a-dodecahydro-2,5,8-trimethyl-1,4,7,96-tetra-azaphenalene)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000760</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pachler</surname>
<given-names>K. G. R.</given-names></name>
<name><surname>Parrish</surname>
<given-names>J. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>760</fpage>
<lpage>762</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000760">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000760">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Perfluoro-1,1-dimethylcyclopentane from pyrolysis of perfluorobicyclohexyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000762</article-id><contrib-group><contrib contrib-type="author">
<name><surname>MacKenzie</surname>
<given-names>D. R.</given-names></name>
<name><surname>Wilson</surname>
<given-names>V. H.</given-names></name>
<name><surname>Anderson</surname>
<given-names>E. W.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>762</fpage>
<lpage>764</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000762">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000762">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The solvolysis of 2-pyridyltrimethyl-silane, -germane, and -stannane by alcohols and by water</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000765</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>D. G.</given-names></name>
<name><surname>Webster</surname>
<given-names>D. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>765</fpage>
<lpage>766</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000765">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000765">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Conformation in the cyclotriveratrylene series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000767</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cookson</surname>
<given-names>R. C.</given-names></name>
<name><surname>Halton</surname>
<given-names>B.</given-names></name>
<name><surname>Stevens</surname>
<given-names>I. D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>767</fpage>
<lpage>774</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000767">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000767">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular polarisability. The conformations of some 9-substituted anthracenes as solutes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000775</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Radom</surname>
<given-names>L.</given-names></name>
<name><surname>Ritchie</surname>
<given-names>G. L. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>775</fpage>
<lpage>778</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000775">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000775">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The rearrangement of phenylsulphamic acid to sulphanilic acid in the presence of [&lt;sup&gt;35&lt;/sup&gt;S]sulphuric acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000779</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spillane</surname>
<given-names>W. J.</given-names></name>
<name><surname>Scott</surname>
<given-names>F. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>779</fpage>
<lpage>781</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000779">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000779">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of lead tetra-acetate. Part XIV. The base-catalysed decomposition of lead tetra-acetate in acetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000781</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Poustie</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>781</fpage>
<lpage>784</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000781">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000781">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An electron spin resonance study of the asymmetric solvation of the &lt;i&gt;m&lt;/i&gt;-dinitrobenzene and 3,5-dinitrobenzoate radical anions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000785</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Griffiths</surname>
<given-names>W. E.</given-names></name>
<name><surname>Gutch</surname>
<given-names>C. J. W.</given-names></name>
<name><surname>Longster</surname>
<given-names>G. F.</given-names></name>
<name><surname>Myatt</surname>
<given-names>J.</given-names></name>
<name><surname>Todd</surname>
<given-names>P. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>785</fpage>
<lpage>789</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000785">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000785">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The secondary isotope effect of deuterium on the ionization constants of some compounds in the pyridine series</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000789</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Batts</surname>
<given-names>B. D.</given-names></name>
<name><surname>Spinner</surname>
<given-names>E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>789</fpage>
<lpage>795</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000789">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000789">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The pyridine-catalysed acetylation of phenols and alcohols by acetic anhydride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000795</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bonner</surname>
<given-names>T. G.</given-names></name>
<name><surname>McNamara</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>795</fpage>
<lpage>797</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000795">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000795">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>An electron spin resonance study of the radicals formed on photolysis of &lt;i&gt;m&lt;/i&gt;-dinitrobenzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000798</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gough</surname>
<given-names>T. E.</given-names></name>
<name><surname>Gross</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>798</fpage>
<lpage>800</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000798">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000798">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electrophilic aromatic substitution. Part I. The nitration of some reactive aromatic compounds in concentrated sulphuric and perchloric acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000800</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coombes</surname>
<given-names>R. G.</given-names></name>
<name><surname>Moodie</surname>
<given-names>R. B.</given-names></name>
<name><surname>Schofield</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>800</fpage>
<lpage>804</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000800">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000800">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Gas-phase eliminations. Part VII. The pyrolysis of substituted 1-phenylethyl chlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000805</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bridge</surname>
<given-names>M. R.</given-names></name>
<name><surname>Davies</surname>
<given-names>D. H.</given-names></name>
<name><surname>Maccoll</surname>
<given-names>Allan</given-names></name>
<name><surname>Ross</surname>
<given-names>R. A.</given-names></name>
<name><surname>Stephenson</surname>
<given-names>B.</given-names></name>
<name><surname>Banjoko</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>805</fpage>
<lpage>808</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000805">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000805">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The effects of structure and of ring-size upon some properties of mono- and di-alkoxybenzoic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000809</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Byrne</surname>
<given-names>(Miss) Monica M.</given-names></name>
<name><surname>Smith</surname>
<given-names>N. H. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>809</fpage>
<lpage>812</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000809">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000809">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Liquid-phase photolysis. Part XII. Evidence from nuclear magnetic resonance for stereospecific electronic ground-state interaction between benzene and maleic anhydride and some maleimides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000812</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bryce-Smith</surname>
<given-names>D.</given-names></name>
<name><surname>Hems</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>812</fpage>
<lpage>815</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000812">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000812">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Liquid-phase photolysis. Part XIII. Charge-transfer transitions in complexes of benzene and alkylbenzenes with tetracyanoethylene, &lt;i&gt;p&lt;/i&gt;-chloranil, and maleic anhydride: use of the aromatic donors as solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000816</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bryce-Smith</surname>
<given-names>D.</given-names></name>
<name><surname>Connett</surname>
<given-names>B. E.</given-names></name>
<name><surname>Gilbert</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>816</fpage>
<lpage>822</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000816">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000816">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The formation, under kinetic control, of a new monoacetal (2,3-&lt;i&gt;O&lt;/i&gt;-butylidene-D-glucitol) from D-glucitol and n-butyraldehyde</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000822</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bonner</surname>
<given-names>T. G.</given-names></name>
<name><surname>Bourne</surname>
<given-names>E. J.</given-names></name>
<name><surname>Cleare</surname>
<given-names>P. J. V.</given-names></name>
<name><surname>Lewis</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>822</fpage>
<lpage>827</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000822">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000822">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetic and thermodynamic control in the formation of monoacetals from aldehydes and D-glucitol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000827</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bonner</surname>
<given-names>T. G.</given-names></name>
<name><surname>Bourne</surname>
<given-names>E. J.</given-names></name>
<name><surname>Cleare</surname>
<given-names>P. J. V.</given-names></name>
<name><surname>Lewis</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>827</fpage>
<lpage>830</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000827">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000827">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;N&lt;/i&gt;-oxides and related compounds. Part XXXIII. The mechanism of the acetic anhydride rearrangement of 2-alkylpyridine 1-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000831</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bodalski</surname>
<given-names>R.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>831</fpage>
<lpage>838</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000831">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000831">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of keten acetals. Part I. The hydrolysis of cyanoketen dimethyl acetal; general acid catalysis and kinetic hydrogen isotope effects</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000839</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
<name><surname>Waterman</surname>
<given-names>D. C. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>839</fpage>
<lpage>849</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000839">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000839">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of keten acetals. Part II. The hydrolysis of 2-dichloromethylene-1,3-dioxolan: general acid catalysis and rate and product hydrogen isotope effects</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000849</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gold</surname>
<given-names>V.</given-names></name>
<name><surname>Waterman</surname>
<given-names>D. C. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>849</fpage>
<lpage>855</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000849">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000849">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation and alkylation reactions. Part III. The interaction of aryloxyacetyl chlorides with aluminium chloride in aromatic solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000856</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Palmer</surname>
<given-names>M. H.</given-names></name>
<name><surname>McVie</surname>
<given-names>G. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>856</fpage>
<lpage>859</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000856">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000856">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Charge-transfer complexes. Part V. Nature of the interaction of halogenomethanes and aromatic hydrocarbons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000859</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davis</surname>
<given-names>K. M. C.</given-names></name>
<name><surname>Farmer</surname>
<given-names>M. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>859</fpage>
<lpage>862</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000859">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000859">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The kinetics and mechanism of the electrophilic substitution of heteroaromatic compounds. Part XIII. The mononitration of 2-phenylpyridine and its &lt;i&gt;N&lt;/i&gt;-oxide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000862</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Kingsland</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>862</fpage>
<lpage>864</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000862">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000862">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The kinetics and mechanism of the electrophilic substitution of heteroaromatic compounds. Part XIV. Rates of acid-catalysed hydrogen exchange of &lt;i&gt;para&lt;/i&gt;-substituted anilines and heterocyclic analogues</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000864</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bean</surname>
<given-names>G. P.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>864</fpage>
<lpage>866</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000864">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000864">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The kinetics and mechanism of electrophilic substitution of heteroaromatic compounds. Part XV. Hydrogen exchange of 3,5-dimethylphenol and heterocyclic analogues</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000866</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bellingham</surname>
<given-names>P.</given-names></name>
<name><surname>Johnson</surname>
<given-names>C. D.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>866</fpage>
<lpage>873</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000866">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000866">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The kinetics and mechanism of electrophilic substitution of heteroaromatic compounds. Part XVI. Acid-catalysed hydrogen exchange of some pyridazine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000873</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Pojarlieff</surname>
<given-names>I.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>873</fpage>
<lpage>877</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000873">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000873">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The stereochemistry of the solvolysis of 2-silylpyridines by methanol and by water</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000878</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>D. G.</given-names></name>
<name><surname>Webster</surname>
<given-names>D. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>878</fpage>
<lpage>879</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000878">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000878">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The carbonyl group frequency. Part II. Aliphatic carboxylic esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000880</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Morgan</surname>
<given-names>K. J.</given-names></name>
<name><surname>Unwin</surname>
<given-names>N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>880</fpage>
<lpage>884</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000880">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000880">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation. Part XXVI. The kinetics and mechanism of the addition of carboxylic acids to ketens in diethyl ether and in dichlorobenzene solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000885</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Briody</surname>
<given-names>J. M.</given-names></name>
<name><surname>Lillford</surname>
<given-names>P. J.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>885</fpage>
<lpage>889</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000885">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000885">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation. Part XXVII. The kinetics and mechanism of the spontaneous and acid-catalysed reactions of dimethylketen with water and alcohols</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000889</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lillford</surname>
<given-names>P. J.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>889</fpage>
<lpage>897</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000889">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000889">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Acylation. Part XXVIII. The kinetics and mechanism of the addition of hydrogen halides to dimethylketen in ether solution. Relative reactivities of substrates towards ketens and a comparison with mechanism of acylation by other acylating agents in non-hydroxylic solvents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000897</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lillford</surname>
<given-names>P. J.</given-names></name>
<name><surname>Satchell</surname>
<given-names>D. P. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>897</fpage>
<lpage>901</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000897">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000897">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Homolytic aromatic substitution by heterocyclic free radicals. Part II. 3-Thienyl radicals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000901</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Martelli</surname>
<given-names>G.</given-names></name>
<name><surname>Spagnolo</surname>
<given-names>P.</given-names></name>
<name><surname>Tiecco</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>901</fpage>
<lpage>905</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000901">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000901">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of the catalytic dehydration of ethanol over alumina</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000905</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Butler</surname>
<given-names>J. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>905</fpage>
<lpage>908</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000905">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000905">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Spectroscopic studies. Part IX. Infrared spectra and structure of some cyclobutanecarboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000908</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thomas</surname>
<given-names>T. H.</given-names></name>
<name><surname>Williams</surname>
<given-names>A. J. S.</given-names></name>
<name><surname>Orville-Thomas</surname>
<given-names>W. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>908</fpage>
<lpage>913</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000908">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000908">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Iodine atom-catalysed isomerisation of symmetrically substituted &lt;i&gt;cis&lt;/i&gt;-stilbenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000913</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Muizebelt</surname>
<given-names>W. J.</given-names></name>
<name><surname>Nivard</surname>
<given-names>R. J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>913</fpage>
<lpage>920</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000913">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000913">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Iodine-catalysed isomerisation of &lt;i&gt;p&lt;/i&gt;-methoxy-&lt;i&gt;cis&lt;/i&gt;-stilbene at room temperature, an ionic reaction</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000921</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Muizebelt</surname>
<given-names>W. J.</given-names></name>
<name><surname>Nivard</surname>
<given-names>R. J. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>921</fpage>
<lpage>922</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000921">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000921">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The structure of camptothecin: &lt;i&gt;X&lt;/i&gt;-ray analysis of camptothecin iodoacetate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000923</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McPhail</surname>
<given-names>A. T.</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>923</fpage>
<lpage>928</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000923">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000923">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The stereochemistry of the reaction of phosphonous and phosphinous halides with 1,3-dienes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000929</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bond</surname>
<given-names>A.</given-names></name>
<name><surname>Green</surname>
<given-names>M.</given-names></name>
<name><surname>Pearson</surname>
<given-names>S. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>929</fpage>
<lpage>931</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000929">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000929">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Conformation and reactivity. Part VIII. Kinetics of the esterification with diazodiphenylmethane in toluene of the &lt;i&gt;trans&lt;/i&gt;-decalincarboxylic acids, of the 4-t-butylcyclohexanecarboxylic acids, of certain &lt;i&gt;trans&lt;/i&gt;-4-substituted cyclohexanecarboxylic acids, and of cyclohexanecarboxylic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000931</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chapman</surname>
<given-names>N. B.</given-names></name>
<name><surname>Ehsan</surname>
<given-names>A.</given-names></name>
<name><surname>Shorter</surname>
<given-names>J.</given-names></name>
<name><surname>Toyne</surname>
<given-names>K. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>931</fpage>
<lpage>933</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000931">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000931">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electronic absorption spectra of some α-cycloalkyl derivatives of Michler's Hydrol Blue</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000933</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hallas</surname>
<given-names>G.</given-names></name>
<name><surname>Schofield</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>933</fpage>
<lpage>935</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000933">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000933">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The crystal structure of &lt;i&gt;syn&lt;/i&gt;-9-benzonorbornenyl &lt;i&gt;p&lt;/i&gt;-bromobenzenesulphonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000935</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sato</surname>
<given-names>T.</given-names></name>
<name><surname>Shiro</surname>
<given-names>M.</given-names></name>
<name><surname>Koyama</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>935</fpage>
<lpage>944</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000935">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000935">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>γ-Radiolysis of ethylene glycol aqueous solutions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000945</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ahmad</surname>
<given-names>Mukhtar</given-names></name>
<name><surname>Awan</surname>
<given-names>Mohammad Hussain</given-names></name>
<name><surname>Mohammad</surname>
<given-names>Din</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>945</fpage>
<lpage>946</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000945">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000945">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Redox transfer. Part V. Elementary steps. The oxidation of ferrous and cuprous chloride by carbon tetrachloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000947</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Asscher</surname>
<given-names>M.</given-names></name>
<name><surname>Vofsi</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>947</fpage>
<lpage>952</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000947">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000947">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance studies of aliphatic nitroxides. Part III. A conformational study of radicals from 4-alkylpiperidines and piperazine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000953</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hudson</surname>
<given-names>A.</given-names></name>
<name><surname>Hussain</surname>
<given-names>H. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>953</fpage>
<lpage>955</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000953">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000953">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The effect of naphthacene on the photo-oxidation of chlorophyll &lt;i&gt;b&lt;/i&gt;</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000955</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sykes</surname>
<given-names>A.</given-names></name>
<name><surname>Truscott</surname>
<given-names>T. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>955</fpage>
<lpage>957</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000955">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000955">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic reactions in ethylenic derivatives. Part XI. Substitution and elimination in β-halogenostyrenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000958</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Marchese</surname>
<given-names>G.</given-names></name>
<name><surname>Naso</surname>
<given-names>F.</given-names></name>
<name><surname>Modena</surname>
<given-names>G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>958</fpage>
<lpage>962</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000958">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000958">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular conformations. Part VI. The structure of withaferin A: &lt;i&gt;X&lt;/i&gt;-ray analysis of withaferin A acetate &lt;i&gt;p&lt;/i&gt;-bromobenzoate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000962</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McPhail</surname>
<given-names>A. T.</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>962</fpage>
<lpage>972</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000962">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000962">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Anodic oxidation of amines. Part I. Cyclic voltammetry of aliphatic amines at a stationary glassy-carbon electrode</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000973</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Masui</surname>
<given-names>Masaichiro</given-names></name>
<name><surname>Sayo</surname>
<given-names>Hiroteru</given-names></name>
<name><surname>Tsuda</surname>
<given-names>Yoshiaki</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>973</fpage>
<lpage>976</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000973">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000973">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Neighbouring-group participation in pyrolysis of aryl azides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000976</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dyall</surname>
<given-names>L. K.</given-names></name>
<name><surname>Kemp</surname>
<given-names>J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>976</fpage>
<lpage>979</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000976">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000976">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;X&lt;/i&gt;-Ray investigation of several phorbol derivatives. The crystal and molecular structure of phorbol bromofuroate–chloroform solvate at –160°</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000980</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pettersen</surname>
<given-names>R. C.</given-names></name>
<name><surname>Birnbaum</surname>
<given-names>G. I.</given-names></name>
<name><surname>Ferguson</surname>
<given-names>G.</given-names></name>
<name><surname>Islam</surname>
<given-names>K. M. S.</given-names></name>
<name><surname>Sime</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>980</fpage>
<lpage>984</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000980">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000980">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The molecular structure of the oxidised condensation product of &lt;i&gt;o&lt;/i&gt;-benzoylbenzaldehyde and ethylenediamine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000984</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McKechnie</surname>
<given-names>James S.</given-names></name>
<name><surname>Paul</surname>
<given-names>Iain C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>984</fpage>
<lpage>988</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000984">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000984">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Metal complexes of thio-hydroxamic acids. Part I. Crystal structure of bis(thioacetohydroxamato)nickel(II)</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000989</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sato</surname>
<given-names>T.</given-names></name>
<name><surname>Shiro</surname>
<given-names>M.</given-names></name>
<name><surname>Koyama</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>989</fpage>
<lpage>994</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000989">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000989">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of lead tetra-acetate. Part XV. The oxidation of α- and &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-β-methylstyrene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680000994</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Norman</surname>
<given-names>R. O. C.</given-names></name>
<name><surname>Thomas</surname>
<given-names>C. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>994</fpage>
<lpage>1005</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680000994">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680000994">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reaction of O(2&lt;sup&gt;3&lt;/sup&gt;&lt;i&gt;P&lt;/i&gt;) atoms with 1,1-difluoro-olefins</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001005</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mitchell</surname>
<given-names>R. C.</given-names></name>
<name><surname>Simons</surname>
<given-names>J. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1005</fpage>
<lpage>1007</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001005">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001005">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The solvolysis of silicon substituted 2-silylpyridines by alcohols and by water</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001008</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Anderson</surname>
<given-names>D. G.</given-names></name>
<name><surname>Webster</surname>
<given-names>D. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1008</fpage>
<lpage>1009</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001008">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001008">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Charge-transfer complexes. Part VI. Solvent shifts of the charge-transfer bands of complexes involving organic ions as donors and acceptors</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001010</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Beaumont</surname>
<given-names>T. G.</given-names></name>
<name><surname>Davis</surname>
<given-names>K. M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1010</fpage>
<lpage>1014</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001010">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001010">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The pyrolysis of 2-methyl-2-nitrosopropane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001014</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Gowenlock</surname>
<given-names>B. G.</given-names></name>
<name><surname>Healey</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1014</fpage>
<lpage>1017</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001014">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001014">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chlorination of αβ-unsaturated carbonyl compounds. Part II. The mechanism of chlorination of &lt;i&gt;para&lt;/i&gt;-substituted methyl &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-cinnamates in acetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001018</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
<name><surname>Trachtenberg</surname>
<given-names>E. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1018</fpage>
<lpage>1022</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001018">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001018">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chlorination of αβ-unsaturated carbonyl compounds. Part III. Reaction of chlorine with &lt;i&gt;trans&lt;/i&gt;-cinnamic acid and the &lt;i&gt;trans&lt;/i&gt;-cinnamate ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001022</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cabaleiro</surname>
<given-names>Mercedes C.</given-names></name>
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
<name><surname>Swedlund</surname>
<given-names>B. E.</given-names></name>
<name><surname>Williams</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1022</fpage>
<lpage>1026</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001022">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001022">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Chlorination of αβ-unsaturated carbonyl compounds. Part IV. Kinetics and mechanism of the uncatalysed and hydrogen chloride catalysed chlorination of &lt;i&gt;trans&lt;/i&gt;-cinnamaldehyde in acetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001026</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cabaleiro</surname>
<given-names>Mercedes C.</given-names></name>
<name><surname>Cooksey</surname>
<given-names>C. J.</given-names></name>
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
<name><surname>Swedlund</surname>
<given-names>B. E.</given-names></name>
<name><surname>Williams</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1026</fpage>
<lpage>1030</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001026">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001026">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism and thermodynamics of chlorine transfer among organochlorinating agents. Part III. Autocatalytic pathway between &lt;i&gt;N&lt;/i&gt;-chloro-succinimide and chloramine-T</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001031</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Higuchi</surname>
<given-names>T.</given-names></name>
<name><surname>Ikeda</surname>
<given-names>K.</given-names></name>
<name><surname>Hussain</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1031</fpage>
<lpage>1036</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001031">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001031">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aspects of tautomerism. Part I. Environmental and substituent effects on the tautomerism of &lt;i&gt;o&lt;/i&gt;-benzoyl benzoic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001036</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bhatt</surname>
<given-names>M. V.</given-names></name>
<name><surname>Kamath</surname>
<given-names>K. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1036</fpage>
<lpage>1044</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001036">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001036">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Unimolecular decomposition of triethylborine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001044</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abuin</surname>
<given-names>E.</given-names></name>
<name><surname>Grotewold</surname>
<given-names>J.</given-names></name>
<name><surname>Lissi</surname>
<given-names>E. A.</given-names></name>
<name><surname>Vara</surname>
<given-names>M. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1044</fpage>
<lpage>1047</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001044">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001044">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;X&lt;/i&gt;-ray studies of terpenoid derivatives. Part I. The crystal and molecular structure of humulene bromohydrin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001047</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Allen</surname>
<given-names>F. H.</given-names></name>
<name><surname>Rogers</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1047</fpage>
<lpage>1063</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001047">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001047">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Substituent effects of positive poles in aromatic substitution. Part V. Variation in the substituent effect of the –NH&lt;sub&gt;3&lt;/sub&gt;&lt;sup&gt;+&lt;/sup&gt; group in aromatic nitration</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001063</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hartshorn</surname>
<given-names>S. R.</given-names></name>
<name><surname>Ridd</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1063</fpage>
<lpage>1067</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001063">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001063">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Substituent effects of positive poles in aromatic substitution. Part VI. The nitration of substituted anilinium ions through proton loss from the –NH&lt;sub&gt;3&lt;/sub&gt;&lt;sup&gt;+&lt;/sup&gt; group</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001068</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hartshorn</surname>
<given-names>S. R.</given-names></name>
<name><surname>Ridd</surname>
<given-names>J. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1068</fpage>
<lpage>1074</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001068">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001068">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Peroxides of elements other than carbon. Part XIV. The mechanism of the autoxidation of organic compounds of lithium, magnesium, zinc, cadmium, and aluminium</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001074</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alwyn G.</given-names></name>
<name><surname>Roberts</surname>
<given-names>B. P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1074</fpage>
<lpage>1078</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001074">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001074">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The unimolecular acid hydrolysis of acetylglycine in aqueous acetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001078</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Martin</surname>
<given-names>R. J. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1078</fpage>
<lpage>1082</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001078">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001078">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Thermal &lt;i&gt;cis&lt;/i&gt;&lt;b&gt;→&lt;/b&gt;&lt;i&gt;trans&lt;/i&gt; isomerization of two dimeric nitrosoalkanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001083</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chaudhry</surname>
<given-names>A. U.</given-names></name>
<name><surname>Gowenlock</surname>
<given-names>B. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1083</fpage>
<lpage>1084</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001083">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001083">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitrones. Part VIII. The ultraviolet absorption of the 1-pyrroline 1-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001085</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kaminsky</surname>
<given-names>L. S.</given-names></name>
<name><surname>Lamchen</surname>
<given-names>M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1085</fpage>
<lpage>1087</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001085">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001085">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;sup&gt;1&lt;/sup&gt;H nuclear magnetic resonance spectra of acetals and thioacetals of 4-piperidones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001087</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Branch</surname>
<given-names>R. F.</given-names></name>
<name><surname>Casy</surname>
<given-names>A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1087</fpage>
<lpage>1089</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001087">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001087">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The effect of pyrolytic carbon coatings on a gas-phase free-radical reaction, the pyrolysis of 1,2-dichloroethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001089</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Holbrook</surname>
<given-names>K. A.</given-names></name>
<name><surname>Walker</surname>
<given-names>R. W.</given-names></name>
<name><surname>Watson</surname>
<given-names>W. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1089</fpage>
<lpage>1094</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001089">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001089">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The nuclear magnetic resonance spectra of fluorobenzenes. Part III. &lt;i&gt;o&lt;/i&gt;-Difluorobenzene and some 1-substituted 2,3-difluorobenzenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001094</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abraham</surname>
<given-names>R. J.</given-names></name>
<name><surname>Cooper</surname>
<given-names>M. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1094</fpage>
<lpage>1098</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001094">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001094">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The hydrolysis of amides, esters, and related compounds in acid solution. Part I. Amides, carbamates, and ureas</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001099</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armstrong</surname>
<given-names>V. C.</given-names></name>
<name><surname>Farlow</surname>
<given-names>D. W.</given-names></name>
<name><surname>Moodie</surname>
<given-names>R. B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1099</fpage>
<lpage>1103</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001099">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001099">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Fungal metabolites. Part VIII. Sesquiterpenoids. Part VII. The structure of fomannosin: &lt;i&gt;X&lt;/i&gt;-ray analysis of dihydrofomannosin &lt;i&gt;p&lt;/i&gt;-bromobenzoylurethane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001104</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McPhail</surname>
<given-names>A. T.</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1104</fpage>
<lpage>1109</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001104">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001104">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The association of dimethylformamide molecules in carbon tetrachloride solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001110</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rabinovitz</surname>
<given-names>Mordecai</given-names></name>
<name><surname>Pines</surname>
<given-names>Alexander</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1110</fpage>
<lpage>1111</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001110">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001110">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aromatic reactivity. Part XXXVII. Detritiation of substituted 1- and 2-tritionaphthalenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001112</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Eaborn</surname>
<given-names>C.</given-names></name>
<name><surname>Golborn</surname>
<given-names>P.</given-names></name>
<name><surname>Spillett</surname>
<given-names>R. E.</given-names></name>
<name><surname>Taylor</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1112</fpage>
<lpage>1123</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001112">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001112">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetic acidity dependence in certain oxidation reactions. Part II. Oxidation of propane-1,3- and butane-1,4-diols by quinquevalent vanadium ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001123</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mehrotra</surname>
<given-names>Raj Narain</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1123</fpage>
<lpage>1127</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001123">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001123">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nuclear magnetic resonance studies of six-membered rings. Part II. Chemical shifts and coupling constants in morpholine and piperazine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001128</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Spragg</surname>
<given-names>R. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1128</fpage>
<lpage>1132</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001128">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001128">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Spiro-conjugation in organic sulphides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001132</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Williams</surname>
<given-names>D. R.</given-names></name>
<name><surname>Coffen</surname>
<given-names>D. L.</given-names></name>
<name><surname>Garrett</surname>
<given-names>P. E.</given-names></name>
<name><surname>Schwartz</surname>
<given-names>R. N.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1132</fpage>
<lpage>1135</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001132">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001132">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The chemistry of terpenes. Part VII. The stereochemistry of the &lt;i&gt;cis&lt;/i&gt;-caranols. Some evidence for their conformational preferences</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001136</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Carson</surname>
<given-names>M. S.</given-names></name>
<name><surname>Cocker</surname>
<given-names>W.</given-names></name>
<name><surname>Grayson</surname>
<given-names>D. H.</given-names></name>
<name><surname>Pratt</surname>
<given-names>A. C.</given-names></name>
<name><surname>Shannon</surname>
<given-names>P. V. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1136</fpage>
<lpage>1140</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001136">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001136">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mass spectrometry of quinones. Part I. Reactions of 1,2-naphthaquinones in the mass spectrometer</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001141</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Oliver</surname>
<given-names>R. W. A.</given-names></name>
<name><surname>Rashman</surname>
<given-names>R. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1141</fpage>
<lpage>1143</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001141">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001141">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The reduction of 9,10-anthraquinones. Part III. Tautomerism of 2-hydroxy-9,10-anthrahydroquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001144</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Broadbent</surname>
<given-names>A. D.</given-names></name>
<name><surname>Sommermann</surname>
<given-names>E. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1144</fpage>
<lpage>1147</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001144">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001144">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aspects of conformation in ring-substituted 2,4,6-trinitroanilines deduced from absorption spectra</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001147</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kamlet</surname>
<given-names>Mortimer J.</given-names></name>
<name><surname>Minesinger</surname>
<given-names>Richard R.</given-names></name>
<name><surname>Hoffsommer</surname>
<given-names>John C.</given-names></name>
<name><surname>Dacons</surname>
<given-names>Joseph C.</given-names></name>
<name><surname>Adolph</surname>
<given-names>Horst G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1147</fpage>
<lpage>1153</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001147">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001147">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The thermal decomposition of acetic acid</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001153</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blake</surname>
<given-names>P. G.</given-names></name>
<name><surname>Jackson</surname>
<given-names>G. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1153</fpage>
<lpage>1155</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001153">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001153">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The thermodynamic equilibrium between &lt;i&gt;cis&lt;/i&gt;- and &lt;i&gt;trans&lt;/i&gt;-isomers in stilbene and some derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001156</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fischer</surname>
<given-names>Gabriella</given-names></name>
<name><surname>Muszkat</surname>
<given-names>K. A.</given-names></name>
<name><surname>Fischer</surname>
<given-names>Ernst</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1156</fpage>
<lpage>1158</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001156">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001156">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;d&lt;/i&gt;-Orbital effects in silicon substituted π-electron systems. Part XII. Some spectroscopic properties of alkyl and silyl acetylenes and polyacetylenes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001158</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bock</surname>
<given-names>H.</given-names></name>
<name><surname>Seidl</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1158</fpage>
<lpage>1163</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001158">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001158">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Solvent effects in nuclear magnetic resonance spectroscopy. Part XVI. The influence of steric factors on specific solute–solvent association: a variable temperature study</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001163</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wilson</surname>
<given-names>Robert G.</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1163</fpage>
<lpage>1168</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001163">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001163">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polymerisation of vinyl monomers by transition-metal allyl compounds. Part I</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001168</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ballard</surname>
<given-names>D. G. H.</given-names></name>
<name><surname>Janes</surname>
<given-names>W. H.</given-names></name>
<name><surname>Medinger</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1168</fpage>
<lpage>1175</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001168">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001168">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Polymerisation of vinyl monomers by transition-metal allyl compounds. Part II. The polymerisation of methyl methacrylate initiated by allyl-chromium compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001176</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ballard</surname>
<given-names>D. G. H.</given-names></name>
<name><surname>Medinger</surname>
<given-names>T.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1176</fpage>
<lpage>1182</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001176">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001176">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Cycloadditions of allylic cations to conjugated dienes: stereochemistry</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001182</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hoffmann</surname>
<given-names>H. M. R.</given-names></name>
<name><surname>Joy</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1182</fpage>
<lpage>1186</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001182">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001182">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Rotational isomerism in epifluorohydrin</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001187</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thomas</surname>
<given-names>W. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1187</fpage>
<lpage>1190</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001187">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001187">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;N&lt;/i&gt;-substituted heterocyclic cations. Part VIII. Substituent effects and the acidity of quinolinium ions. Hydroxide addition &lt;i&gt;versus&lt;/i&gt; proton loss</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001191</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooksey</surname>
<given-names>C. J.</given-names></name>
<name><surname>Johnson</surname>
<given-names>M. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1191</fpage>
<lpage>1197</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001191">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001191">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The decomposition of gaseous chloroformates. Part IV. Allylic and benzyl chloroformates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001198</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Lewis</surname>
<given-names>E. S.</given-names></name>
<name><surname>Witte</surname>
<given-names>K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1198</fpage>
<lpage>1200</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001198">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001198">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of the reactions of fluoro- or chloro-2,4-dinitrobenzene with n-butyl-, s-butyl- or t-butyl-amine in benzene. Further evidence for an addition intermediate in nucleophilic aromatic substitution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001200</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pietra</surname>
<given-names>Francesco</given-names></name>
<name><surname>Vitali</surname>
<given-names>Dario</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1200</fpage>
<lpage>1203</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001200">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001200">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular polarisability. The molar Kerr constants of boron trihalides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001203</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Armstrong</surname>
<given-names>R. S.</given-names></name>
<name><surname>Aroney</surname>
<given-names>M. J.</given-names></name>
<name><surname>Hector</surname>
<given-names>(Miss) A.</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1203</fpage>
<lpage>1205</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001203">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001203">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular polarisability. The conformations as solutes of phenothiazine and of &lt;i&gt;N&lt;/i&gt;-methyl- and &lt;i&gt;N&lt;/i&gt;-phenyl-phenothiazine</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001206</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aroney</surname>
<given-names>M. J.</given-names></name>
<name><surname>Hoskins</surname>
<given-names>G. M.</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1206</fpage>
<lpage>1208</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001206">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001206">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A spectroscopic study of the reversible reactions of aromatic nitrocompounds with sulphur bases</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001208</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crampton</surname>
<given-names>M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1208</fpage>
<lpage>1213</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001208">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001208">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in mass spectrometry. Part XXXII. The kinetic approach to mass spectrometry</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001213</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Howe</surname>
<given-names>Ian</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1213</fpage>
<lpage>1217</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001213">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001213">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Elimination–addition. Part XV. Rates of reactions of ω-bromoalkyl &lt;i&gt;p&lt;/i&gt;-tolyl sulphides with alkoxides: the role of neighbouring group participation by sulphur and the involvement of ion-pair equilibria</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001218</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Knipe</surname>
<given-names>A. C.</given-names></name>
<name><surname>Stirling</surname>
<given-names>C. J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1218</fpage>
<lpage>1223</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001218">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001218">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The influence of the stereochemistry of the nitrogen centre on proton chemical shifts and on &lt;sup&gt;1&lt;/sup&gt;H–&lt;sup&gt;1&lt;/sup&gt;H and &lt;sup&gt;15&lt;/sup&gt;N–&lt;sup&gt;1&lt;/sup&gt;H spin–spin coupling in tetrahydro-1,3-oxazines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001224</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Riddell</surname>
<given-names>F. G.</given-names></name>
<name><surname>Lehn</surname>
<given-names>J. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1224</fpage>
<lpage>1228</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001224">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001224">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The crystal and molecular structure of 9α-bromo-17β-hydroxy-17α-methylandrost-4-ene-3,11-dione</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001228</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooper</surname>
<given-names>A.</given-names></name>
<name><surname>Lu</surname>
<given-names>C. T.</given-names></name>
<name><surname>Norton</surname>
<given-names>D. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1228</fpage>
<lpage>1237</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001228">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001228">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Spectroscopic studies of acid halides: fluoroacetyl chloride and fluoroacetyl bromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001237</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Jenkins</surname>
<given-names>J. E. F.</given-names></name>
<name><surname>Ladd</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1237</fpage>
<lpage>1240</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001237">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001237">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular conformations. Part VII. The bicyclo[3,3,1]nonane system: &lt;i&gt;X&lt;/i&gt;-ray analysis of 9-benzoyl-3α-bromo-2β-hydroxy-9-azabicyclo[3,3,1]-nonane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001241</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tamura</surname>
<given-names>Chihiro</given-names></name>
<name><surname>Sim</surname>
<given-names>G. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1241</fpage>
<lpage>1248</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001241">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001241">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular conformations. Part VIII. The bicyclo[2,2,2]octane system: &lt;i&gt;X&lt;/i&gt;-ray analysis of 1-&lt;i&gt;p&lt;/i&gt;-bromobenzenesulphonyloxymethylbicyclo[2,2,2]-octane</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001249</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cameron</surname>
<given-names>A. F.</given-names></name>
<name><surname>Ferguson</surname>
<given-names>G.</given-names></name>
<name><surname>Morris</surname>
<given-names>D. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1249</fpage>
<lpage>1255</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001249">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001249">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Caryophyllene rearrangement products. Part I. The crystal structure and absolute stereochemistry of caryophyllene ‘iodonitrosite’, a stable nitroxide radical</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001255</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hawley</surname>
<given-names>David M.</given-names></name>
<name><surname>Ferguson</surname>
<given-names>George</given-names></name>
<name><surname>Robertson</surname>
<given-names>J. Monteath</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1255</fpage>
<lpage>1261</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001255">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001255">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electrophilic additions to alkenes, part V. Substituent effects on the rates of reaction of arylsulphenyl chlorides with cyclohexene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001262</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>C.</given-names></name>
<name><surname>Hogg</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1262</fpage>
<lpage>1265</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001262">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001262">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Surface problems in kinetic studies of the gas-phase pyrolyses of alkyl halides. Part II. Pyrolyses of alkyl iodides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001265</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Choudhary</surname>
<given-names>G.</given-names></name>
<name><surname>Holmes</surname>
<given-names>J. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1265</fpage>
<lpage>1270</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001265">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001265">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Photochemistry of organic nitrogen compounds. Part IV. The photolysis of 4-alkylidene-1-pyrazolines: a possible route to trismethylenemethyl diradicals</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001271</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Andrews</surname>
<given-names>S. D.</given-names></name>
<name><surname>Day</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1271</fpage>
<lpage>1279</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001271">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001271">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies on benzimidazoles. Part IV. Nucleophilic displacement of &lt;i&gt;N&lt;/i&gt;-substituted 2-halogenobenzimidazoles by thiophenol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001280</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ricci</surname>
<given-names>A.</given-names></name>
<name><surname>Vivarelli</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1280</fpage>
<lpage>1284</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001280">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001280">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Studies in mass spectrometry. Part XXXIII. Hydrogen scrambling in methylpyridines and quinoline</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001284</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cole</surname>
<given-names>W. G.</given-names></name>
<name><surname>Williams</surname>
<given-names>Dudley H.</given-names></name>
<name><surname>Yeo</surname>
<given-names>Adrian N. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1284</fpage>
<lpage>1288</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001284">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001284">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hybridisation in benzene valence isomers by the method of maximum overlap</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001289</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Randić</surname>
<given-names>M.</given-names></name>
<name><surname>Majerski</surname>
<given-names>Z.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1289</fpage>
<lpage>1291</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001289">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001289">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aromatic substitution. Part XX. Homolytic arylation of aromatic compounds with benzenediazonium tetrafluoroborate and pyridine in homogeneous solution</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001292</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Abramovitch</surname>
<given-names>R. A.</given-names></name>
<name><surname>Koleoso</surname>
<given-names>O. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1292</fpage>
<lpage>1294</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001292">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001292">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of the neutral and alkaline hydrolysis of aromatic sulphonyl chlorides in water</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001294</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rogne</surname>
<given-names>O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1294</fpage>
<lpage>1296</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001294">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001294">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The degree of charge-transfer in the ground-states of molecular π-complexes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001297</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Radford</surname>
<given-names>D. V.</given-names></name>
<name><surname>Stiles</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1297</fpage>
<lpage>1302</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001297">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001297">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nucleophilic catalysis. Part II. The acid catalysed hydrolysis of diazo-ketones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001302</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Aziz</surname>
<given-names>Surraiya</given-names></name>
<name><surname>Tillett</surname>
<given-names>J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1302</fpage>
<lpage>1307</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001302">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001302">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Tautomerism in 1-phenylazo-2-naphthols by use of nitrogen-14 nuclear magnetic resonance data</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001308</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Berrie</surname>
<given-names>A. H.</given-names></name>
<name><surname>Hampson</surname>
<given-names>P.</given-names></name>
<name><surname>Longworth</surname>
<given-names>S. W.</given-names></name>
<name><surname>Mathias</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1308</fpage>
<lpage>1310</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001308">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001308">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nitroxide radicals. Part III. The formation of mononitroxides from binitrones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001311</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Forrester</surname>
<given-names>A. R.</given-names></name>
<name><surname>Thomson</surname>
<given-names>R. H.</given-names></name>
<name><surname>Luckhurst</surname>
<given-names>G. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1311</fpage>
<lpage>1315</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001311">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001311">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nuclear magnetic resonance spectra of some aromatic sulphur derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001315</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brown</surname>
<given-names>C.</given-names></name>
<name><surname>Hogg</surname>
<given-names>D. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1315</fpage>
<lpage>1317</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001315">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001315">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aromatic activated nucleophilic substitution. Catalysis by phenols and by salts of piperidinodefluorination in benzene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001318</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pietra</surname>
<given-names>Francesco</given-names></name>
<name><surname>Vitali</surname>
<given-names>Dario</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1318</fpage>
<lpage>1321</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001318">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001318">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Oxidations of organic compounds by cobalt salts. Part XI. Kinetic and product studies of oxidations of some ω-phenylalkanecarboxylic acids</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001322</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Sharan</surname>
<given-names>P. R.</given-names></name>
<name><surname>Smith</surname>
<given-names>P.</given-names></name>
<name><surname>Waters</surname>
<given-names>William A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1322</fpage>
<lpage>1327</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001322">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001322">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron impact-induced rearrangements in compounds having the PS bond</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001327</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cooks</surname>
<given-names>R. G.</given-names></name>
<name><surname>Gerrard</surname>
<given-names>A. F.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1327</fpage>
<lpage>1333</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001327">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001327">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Factors in the formation of isomerically and optically pure alkyl halides. Part VI. The preparation of optically pure 2-halogenobutanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001333</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Goodwin</surname>
<given-names>D. G.</given-names></name>
<name><surname>Hudson</surname>
<given-names>H. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1333</fpage>
<lpage>1336</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001333">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001333">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The nitration of indeno[1,2,3-&lt;i&gt;cd&lt;/i&gt;]fluoranthene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001337</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Davies</surname>
<given-names>Alun</given-names></name>
<name><surname>Warren</surname>
<given-names>Keith D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1337</fpage>
<lpage>1339</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001337">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001337">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Elimination reactions. Part II. Pyrolytic and base-promoted decompositions of thujyl compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001339</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banthorpe</surname>
<given-names>D. V.</given-names></name>
<name><surname>Davies</surname>
<given-names>H. ff. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1339</fpage>
<lpage>1346</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001339">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001339">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance studies of aliphatic nitroxides. Part IV. The observation of conformational effects in medium sized rings</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001346</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hudson</surname>
<given-names>A.</given-names></name>
<name><surname>Hussain</surname>
<given-names>H. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1346</fpage>
<lpage>1348</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001346">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001346">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions of tervalent phosphorus–nitrogen compounds. Part III. Reactions of isocyanates</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001349</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Hudson</surname>
<given-names>R. F.</given-names></name>
<name><surname>Searle</surname>
<given-names>R. J. G.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1349</fpage>
<lpage>1353</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001349">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001349">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydrogen bonding in bi- and tri-cyclic derivatives of salicyclic and 2-hydroxyisophthalic acids and their esters</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001353</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Palmer</surname>
<given-names>M. H.</given-names></name>
<name><surname>Scollick</surname>
<given-names>N. M.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1353</fpage>
<lpage>1355</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001353">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001353">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereochemistry of reduction of (–)-thujone and (—)-isothujone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001356</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Banthorpe</surname>
<given-names>D. V.</given-names></name>
<name><surname>Davies</surname>
<given-names>H. ff. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1356</fpage>
<lpage>1360</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001356">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001356">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The kinetics and mechanism of the alkaline hydrolysis of organic sulphites</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001360</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bristow</surname>
<given-names>P. A.</given-names></name>
<name><surname>Tillett</surname>
<given-names>J. G.</given-names></name>
<name><surname>Wiggins</surname>
<given-names>D. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1360</fpage>
<lpage>1363</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001360">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001360">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The methanolysis of nitrophenyl esters. Part III. The kinetics of the base-catalysed methanolysis and pyridinolysis of 2,4-dinitrophenyl toluene-&lt;i&gt;p&lt;/i&gt;-sulphonate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001364</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Kirkien-Konasiewicz</surname>
<given-names>(Mrs) Alicja</given-names></name>
<name><surname>Sammy</surname>
<given-names>G. M.</given-names></name>
<name><surname>Maccoll</surname>
<given-names>Allan</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1364</fpage>
<lpage>1369</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001364">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001364">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The molecular structure of chloralide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001369</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Chia</surname>
<given-names>L. H. L.</given-names></name>
<name><surname>Huang</surname>
<given-names>H. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1369</fpage>
<lpage>1373</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001369">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001369">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The thermodynamics of the acid dissociation of some alkylammonium ions in water</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001373</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cox</surname>
<given-names>M. C.</given-names></name>
<name><surname>Everett</surname>
<given-names>D. H.</given-names></name>
<name><surname>Landsman</surname>
<given-names>D. A.</given-names></name>
<name><surname>Munn</surname>
<given-names>R. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1373</fpage>
<lpage>1379</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001373">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001373">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The thermodynamics of the acid dissociation of some amino-alcohols in water</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001380</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Timimi</surname>
<given-names>B. A.</given-names></name>
<name><surname>Everett</surname>
<given-names>D. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1380</fpage>
<lpage>1386</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001380">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001380">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The crystal and molecular structure of oestradiol 3-&lt;i&gt;p&lt;/i&gt;-bromobenzoate</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001387</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Tsukuda</surname>
<given-names>Y.</given-names></name>
<name><surname>Sato</surname>
<given-names>T.</given-names></name>
<name><surname>Shiro</surname>
<given-names>M.</given-names></name>
<name><surname>Koyama</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1387</fpage>
<lpage>1393</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001387">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001387">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Proton magnetic resonance spectra of cinnolines. Part II. Alkylated derivatives of 4-substituted cinnolines</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001393</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Ellis</surname>
<given-names>A. W.</given-names></name>
<name><surname>Lovesey</surname>
<given-names>A. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1393</fpage>
<lpage>1396</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001393">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001393">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Correction to paper entitled ‘a kinetic study of the gas-phase thermal decomposition of 1, 1-dimethyl-1-silacyclobutane’</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001396</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flowers</surname>
<given-names>M. C.</given-names></name>
<name><surname>Gusel'nikov</surname>
<given-names>L. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1396</fpage>
<lpage>1396</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001396">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001396">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Measurement of electrophilic aromatic reactivities &lt;i&gt;via&lt;/i&gt; pyrolysis of 1-arylethyl acetates. Part II. The 2- and 3-positions of furan and thiophen</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001397</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1397</fpage>
<lpage>1401</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001397">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001397">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Measurement of electrophilic aromatic reactivities &lt;i&gt;via&lt;/i&gt; pyrolysis of 1-arylethyl acetates. Part III. The 2-position of biphenylene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001402</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Blatchly</surname>
<given-names>J.</given-names></name>
<name><surname>Taylor</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1402</fpage>
<lpage>1403</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001402">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001402">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Azo–hydrazo conversion. Kinetics of isomerization of 1-tosylazocyclohexene to cyclohex-2-enone tosylhydrazone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001404</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Dondoni</surname>
<given-names>A.</given-names></name>
<name><surname>Rossini</surname>
<given-names>G.</given-names></name>
<name><surname>Mossa</surname>
<given-names>G.</given-names></name>
<name><surname>Caglioti</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1404</fpage>
<lpage>1407</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001404">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001404">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The mass spectrometry of nitrate esters and related compounds. Part II</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001407</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Fraser</surname>
<given-names>R. T. M.</given-names></name>
<name><surname>Paul</surname>
<given-names>N. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1407</fpage>
<lpage>1410</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001407">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001407">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The polarography of cyclohexanone and cyclohex-2-en-1-one</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001410</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Denney</surname>
<given-names>E. J.</given-names></name>
<name><surname>Mooney</surname>
<given-names>B.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1410</fpage>
<lpage>1415</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001410">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001410">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism of biphosphine disulphide formation in reactions of thiophosphoryl and phosphonothioic halides with Grignard reagents</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001416</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Crofts</surname>
<given-names>P. C.</given-names></name>
<name><surname>Fox</surname>
<given-names>I. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1416</fpage>
<lpage>1420</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001416">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001416">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron-transfer oxidations of organic compounds. Part II. The oxidation of phenol and 2,6-dimethylphenol by the hexachloroiridate(IV) anion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001420</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cecil</surname>
<given-names>R.</given-names></name>
<name><surname>Littler</surname>
<given-names>J. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1420</fpage>
<lpage>1427</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001420">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001420">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism of the solvolysis of allylic diphenyl phosphates in phenol</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001427</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Miller</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1427</fpage>
<lpage>1431</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001427">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001427">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>1,3,5-Triazines. Part VIII. The reactions of cyanuric chloride with &lt;i&gt;NN&lt;/i&gt;-dialkylnaphthylamines and &lt;i&gt;O&lt;/i&gt;-alkyl naphthyl ethers</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001431</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shaw</surname>
<given-names>R. A.</given-names></name>
<name><surname>Ward</surname>
<given-names>P.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1431</fpage>
<lpage>1435</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001431">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001431">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of reactions in heterocycles. Part V. Replacement of the methylsulphinyl and methylthio-groups in substituted six-membered nitrogen heterocycles by methoxide ion.</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001435</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barlin</surname>
<given-names>G. B.</given-names></name>
<name><surname>Brown</surname>
<given-names>W. V.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1435</fpage>
<lpage>1445</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001435">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001435">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Crystal and molecular structure of a 1 : 1 bullvalene–silver tetrafluoroborate complex</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001445</article-id><contrib-group><contrib contrib-type="author">
<name><surname>McKechnie</surname>
<given-names>James S.</given-names></name>
<name><surname>Paul</surname>
<given-names>Iain C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1445</fpage>
<lpage>1452</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001445">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001445">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Nuclear magnetic resonance solvent effects on some α-methylcyclohexanone oximes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001453</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cavalli</surname>
<given-names>L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1453</fpage>
<lpage>1454</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001453">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001453">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Mechanism of electrophilic substitution at a saturated carbon atom. Part X. Anion-catalysed acidolysis of α-ethoxycarbonylbenzylmercuric chloride</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001455</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Coad</surname>
<given-names>J. R.</given-names></name>
<name><surname>Ingold</surname>
<given-names>C. K.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1455</fpage>
<lpage>1458</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001455">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001455">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conformational analysis of saturated heterocycles. Part XV. 1-t-Butyl-3-methyl- and 1-t-butyl-3,5-dimethyl-4-piperidone and the corresponding 3-ethyl and 3,5-diethyl derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001459</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brignell</surname>
<given-names>P. J.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Russell</surname>
<given-names>P. L.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1459</fpage>
<lpage>1462</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001459">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001459">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conformational analysis of saturated heterocycles. Part XVI. A simple quantitative approach to intramolecular interactions</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001462</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brignell</surname>
<given-names>P. J.</given-names></name>
<name><surname>Brown</surname>
<given-names>K.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1462</fpage>
<lpage>1467</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001462">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001462">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conformational analysis of saturated heterocycles. Part XVII. Sulphonium salt formation by thiacyclohexanes</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001467</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Cook</surname>
<given-names>M. J.</given-names></name>
<name><surname>Dorn</surname>
<given-names>H.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1467</fpage>
<lpage>1470</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001467">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001467">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The conformational analysis of saturated heterocycles. Part XVIII. The orientation of NH-groups in piperidines and morpholines from infrared spectroscopy</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001470</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Baldock</surname>
<given-names>R. W.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1470</fpage>
<lpage>1477</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001470">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001470">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The kinetics and mechanism of electrophilic substitution of heteroaromatic compounds. Part XVII. The nitration of pyridones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001477</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brignell</surname>
<given-names>P. J.</given-names></name>
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Tarhan</surname>
<given-names>H. O.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1477</fpage>
<lpage>1484</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001477">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001477">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The kinetics and mechanism of electrophilic substitution of heteroaromatic compounds. Part XIX. Acid-catalysed hydrogen exchange of some pyrimidine derivatives</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001484</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Katritzky</surname>
<given-names>A. R.</given-names></name>
<name><surname>Kingsland</surname>
<given-names>M.</given-names></name>
<name><surname>Tee</surname>
<given-names>O. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1484</fpage>
<lpage>1491</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001484">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001484">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Gas-phase eliminations. Part VIII. The effect of β-methylation on the pyrolysis of some t-alkyl chlorides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001492</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Maccoll</surname>
<given-names>Allan</given-names></name>
<name><surname>Wong</surname>
<given-names>(Miss) S. C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1492</fpage>
<lpage>1494</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001492">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001492">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The kinetics of solvolysis and peroxide decomposition of purpurogalloquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001494</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Collier</surname>
<given-names>P. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1494</fpage>
<lpage>1499</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001494">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001494">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Spectroscopic studies on carbonium ions derived from aromatic olefins. Part III. Ions derived from styrene and cognate compounds</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001500</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bertoli</surname>
<given-names>V.</given-names></name>
<name><surname>Plesch</surname>
<given-names>P. H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1500</fpage>
<lpage>1516</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001500">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001500">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>&lt;i&gt;N&lt;/i&gt;-oxides and related compounds. Part XXXIV. The tautomerism of some naphtho-and quinolino-furoxans</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001516</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1516</fpage>
<lpage>1523</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001516">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001516">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Aromatic sulphonation. Part XXII. Kinetic isotope effects in the reaction of [1,3,5-&lt;sup&gt;2&lt;/sup&gt;H&lt;sub&gt;3&lt;/sub&gt;]benzene with sulphur trioxide: competitive sulphonation of benzene and toluene</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001524</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bosscher</surname>
<given-names>J. K.</given-names></name>
<name><surname>Cerfontain</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1524</fpage>
<lpage>1526</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001524">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001524">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of the photochromic decay reaction of 2,2′,4,4′,5,5′-hexaphenyl-bi-imidazolyl</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001526</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wilks</surname>
<given-names>M. A. J.</given-names></name>
<name><surname>Willis</surname>
<given-names>M. R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1526</fpage>
<lpage>1529</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001526">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001526">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Reactions in strongly basic solutions. Part I. Kinetics and mechanism of the alkylation and benzylation of the 9-cyanofluorenyl anion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001529</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bowden</surname>
<given-names>K.</given-names></name>
<name><surname>Cook</surname>
<given-names>R. S.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1529</fpage>
<lpage>1533</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001529">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001529">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Proton nuclear magentic resonance spectra of some &lt;i&gt;N&lt;/i&gt;-substituted 3-amino-4-phenylcyclobutenediones</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001534</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Thorpe</surname>
<given-names>J. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1534</fpage>
<lpage>1535</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001534">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001534">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Diazepines. Part VIII. Equilibria and entropy changes in condensation reactions leading to 2,3-dihydro-1,4-diazepines. Ultraviolet and infrared spectra of products</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001536</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barnett</surname>
<given-names>C.</given-names></name>
<name><surname>Marshall</surname>
<given-names>D. R.</given-names></name>
<name><surname>Lloyd</surname>
<given-names>D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1536</fpage>
<lpage>1544</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001536">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001536">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Amaryllidaceae alkaloids. Part I. The crystal structure of dihydrolycorine hydrobromide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001544</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Shiro</surname>
<given-names>M.</given-names></name>
<name><surname>Sato</surname>
<given-names>T.</given-names></name>
<name><surname>Koyama</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1544</fpage>
<lpage>1551</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001544">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001544">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Molecular polarisability. The conformations of some polynuclear aromatic hydrocarbons</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001551</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Bergmann</surname>
<given-names>E. D.</given-names></name>
<name><surname>Rabinovitz</surname>
<given-names>M.</given-names></name>
<name><surname>Aroney</surname>
<given-names>M. J.</given-names></name>
<name><surname>Fèvre</surname>
<given-names>R. J. W. Le</given-names></name>
<name><surname>Radom</surname>
<given-names>L.</given-names></name>
<name><surname>Ritchie</surname>
<given-names>G. L. D.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1551</fpage>
<lpage>1554</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001551">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001551">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>A kinetic and mechanistic study of the cyclisation of 2′-carboxy-4-bromocarbanilide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001554</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>P. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1554</fpage>
<lpage>1559</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001554">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001554">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electrophilic aromatic substitution. Part III. The effect of strain on the electrophilic reactivity of fluorene, dibenzofuran, dibenzothiophen, and carbazole</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001559</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Taylor</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1559</fpage>
<lpage>1562</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001559">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001559">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetic acidity dependence in certain oxidation reactions. Part III. Oxidation of citric acid by quinquevalent vanadium ion</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001563</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Mehrotra</surname>
<given-names>Raj Narain</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1563</fpage>
<lpage>1566</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001563">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001563">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Stereochemistry of carbohydrate derivatives. Part I. &lt;i&gt;X&lt;/i&gt;-Ray analysis of the adduct formed by addition of dichloromethylene to 3-deoxy-1,2:5,6-di-&lt;i&gt;O&lt;/i&gt;-isopropylidene-α-D-&lt;i&gt;erythro&lt;/i&gt;-hex-3-enofuranose</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001566</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Brimacombe</surname>
<given-names>J. S.</given-names></name>
<name><surname>Gent</surname>
<given-names>(Miss) P. A.</given-names></name>
<name><surname>Hamor</surname>
<given-names>T. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1566</fpage>
<lpage>1571</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001566">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001566">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Kinetics of acid-catalyzed deuteriation of the 2,3-dihydro-5,7-dimethyl-1,4-diazepinium cation</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001572</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Barnett</surname>
<given-names>C.</given-names></name>
<name><surname>Warkentin</surname>
<given-names>J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1572</fpage>
<lpage>1574</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001572">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001572">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The &lt;sup&gt;1&lt;/sup&gt;&lt;i&gt;B&lt;/i&gt;&lt;sub&gt;2&lt;i&gt;u&lt;/i&gt;&lt;/sub&gt;←&lt;sup&gt;1&lt;/sup&gt;&lt;i&gt;A&lt;/i&gt;&lt;sub&gt;1&lt;i&gt;g&lt;/i&gt;&lt;/sub&gt; transition of benzene and of some deuteriated benzenes: solvent and temperature effects</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001574</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Trombetti</surname>
<given-names>A.</given-names></name>
<name><surname>Zauli</surname>
<given-names>C.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1574</fpage>
<lpage>1577</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001574">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001574">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Hydrogen bonding in pyridine &lt;i&gt;N&lt;/i&gt;-oxides</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001578</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Trombetti</surname>
<given-names>A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1578</fpage>
<lpage>1580</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001578">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001578">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Electron spin resonance study of radicals photolytically generated from aromatic carbonyl compounds. Part II. Hydroxy-radicals from acetophenone, xanthone, thioxanthone, &lt;i&gt;p&lt;/i&gt;-hydroxybenzophenone, perinaphthenone and &lt;i&gt;p&lt;/i&gt;-benzoquinone</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001581</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Wilson</surname>
<given-names>R.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1581</fpage>
<lpage>1588</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001581">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001581">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>The proton magnetic resonance spectra of hexahydropyrrolizine, its salts, its 3-methyl derivatives, and its methiodide</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001589</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Skvortsov</surname>
<given-names>Igor M.</given-names></name>
<name><surname>Elvidge</surname>
<given-names>J. A.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1589</fpage>
<lpage>1595</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001589">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001589">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Activated aromatic substitution by piperidine or [1-&lt;sup&gt;2&lt;/sup&gt;H]piperidine in benzene. Dependence of kinetic deuterium isotope effect on the group displaced</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001595</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Pietra</surname>
<given-names>Francesco</given-names></name>
<name><surname>Vitali</surname>
<given-names>Dario</given-names></name>
<name><surname>Frediani</surname>
<given-names>Sergio</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1595</fpage>
<lpage>1600</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001595">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001595">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Index of authors, 1968</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001601</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1601</fpage>
<lpage>1613</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001601">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001601">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Index of subjects, 1968</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J29680001615</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>1615</fpage>
<lpage>1633</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J29680001615">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J29680001615">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Carbon-13 n.m.r. Spectroscopy of pyrazole and some substituted pyrazoles</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J2968000387a</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Rees</surname>
<given-names>R. G.</given-names></name>
<name><surname>Green</surname>
<given-names>M. J.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>387a</fpage>
<lpage>387a</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J2968000387a">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J2968000387a">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Trichloronitrosomethane. Part I. Physicochemical studies</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J2968000387b</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Briden</surname>
<given-names>A. R.</given-names></name>
<name><surname>Price</surname>
<given-names>D.</given-names></name>
<name><surname>Sutcliffe</surname>
<given-names>H.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>387b</fpage>
<lpage>389</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J2968000387b">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J2968000387b">PDF</self-uri>
</article-meta>
</front>
<article-type>research-article</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Errata</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J2968000X001</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Flowers</surname>
<given-names>M. C.</given-names></name>
<name><surname>Gusel'Nikov</surname>
<given-names>L. E.</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>X001</fpage>
<lpage>X007</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J2968000X001">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J2968000X001">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
<article>
<front>
<journal-meta>
<journal-title>Journal of the Chemical Society B: Physical Organic</journal-title>
<issn></issn>
<publisher>
<publisher-name>Royal Society of Chemistry</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<title-group>
<article-title>Errata</article-title>
</title-group>
<article-id pub-id-type="doi">10.1039/J2968000X008</article-id><contrib-group><contrib contrib-type="author">
<name><surname>Author</surname><given-names>Anonymous</given-names></name>
</contrib></contrib-group>
<pub-date pub-type="pub"><year>1968</year></pub-date>
<volume>1968</volume>
<issue />
<fpage>X008</fpage>
<lpage>X0014</lpage>
<self-uri xlink:href="http://xlink.rsc.org/?DOI=J2968000X008">Abstract</self-uri>
<self-uri xlink:href="http://pubs.rsc.org/en/Content/ArticlePDF/1968/J2/J2968000X008">PDF</self-uri>
</article-meta>
</front>
<article-type>other</article-type>
</article>
</articles>
