Dehydration of ethanol to form ethene
Class practical or demonstration
vapour is Ethanol
by passing over a heated catalyst to produce dehydrated gas. This is collected over water and tested for typical properties of an ethene . unsaturated hydrocarbon
The experiment can be performed as a demonstration or as a class experiment according to circumstances. The main risk to be considered in making the choice is the reliability of the student’s involved handling very hot glassware and manipulating the apparatus for safe gas collection over water, while avoiding suck-back of cold water into the hot tube.
A demonstration will take about 10 - 15 minutes, with a few more minutes for testing the gases. A class experiment takes longer, probably about 30 - 40 minutes.
Alternatively the teacher could demonstrate the dehydration but get the students to perform the test-tube tests for the product.
The teacher and/or each working group will require:
Safety screens (for demonstration)
Boiling tube (Note 1)
Rubber bung, 1 hole – to fit boiling tube
Delivery tube (see diagram)
Bunsen valve (Note 2)
Corks or bungs, to fit test tubes, 6
Heat resistant mat
Glass or plastic trough, small (Note 3)
Retort stand, boss and clamp
Ethanol (IDA, Industrial Denatured Alcohol) (HIGHLY FLAMMABLE, HARMFUL), 2 - 3 cm
3 (provided in small bottles)
Mineral wool, sufficient for a loosely-packed wad to absorb the liquid at the bottom of the test-tube
Pumice stone or porous pot (unglazed), a supply of small fragments - about pea-sized
Bromine water, 0.02 M (HARMFUL), about 5 cm
3 - diluted to pale orange-brown
Acidified potassium manganate(VII) (potassium permanganate) solution, about 0.01 M, about
5 cm 3 (Note 4)
Refer to Health & Safety and Technical notes section below for additional information.
Health & Safety and Technical notes
Read our standard health & safety guidance
Ethanol (IDA, Industrial Denatured Alcohol) (HIGHLY FLAMMABLE, HARMFUL) - see CLEAPSS
Bromine water (HARMFUL) - see CLEAPSS
Potassium manganate(VII) (potassium permanganate) solution, about 0.01 M - see CLEAPSS
Hazcard and CLEAPSS Recipe Book.
Dilute sulfuric acid, 0.1 M - see CLEAPSS H
azcard and CLEAPSS Recipe Book.
The assembled apparatus needs to look like this:
A large, 150 x 25 mm, hard glass (borosilicate) test-tube. 1
The purpose of the Bunsen valve (see diagram below) is to prevent suck-back of water into the hot tube when heating is stopped and the gas inside the apparatus contracts on cooling. The Bunsen valve is constructed from a short length (about 3 cm) of clean, unused, soft rubber tubing, with one end stoppered with a short length of glass rod. A 1 cm long slit is carefully cut into the middle of the rubber tubing with a scalpel. The resulting assembly is fitted onto the lower end of the delivery tube. Note that the effectiveness of the home-made valve is variable, and for class use a supply of spares should be provided. 2
The trough needs to be small enough to match the scale of gas collection – the large traditional trough which used to be used with gas jars is not appropriate. For demonstration or class use square, clear, plastic sandwich boxes make excellent troughs. 3
The potassium permanganate(VII) solution is made by dissolving solid potassium permanganate(VII) in 0.1 M sulfuric acid. 1 dm 4
3 of stock solution is made by dissolving 1.6 g of potassium permanganate(VII) crystals in 1 dm 3 of 0.1 M sulfuric acid.
For a demonstration, the class and teacher should be protected by safety screens in case of unexpected suck-back causing the hot tube to shatter on a demonstration bench.
Assemble the apparatus within easy reach of a Bunsen flame.
a Half fill the trough with water and fill the test-tubes with water, leaving them submerged in the trough. Bungs for the test-tubes can be placed upside-down in the trough, so that the tubes filled with gas can just be pressed onto them before they are removed to a rack.
b Place a wad of mineral wool in the bottom of the boiling tube so that it fills the bottom to a depth of about 1 cm without packing too firmly. Using a dropping pipette, carefully drop about 2 cm 3 of ethanol into the mineral wool so that it soaks in. It should be possible to invert the tube without any significant amount of liquid draining out.
c Clamp the boiling tube at the neck end so that the mouth is tilted slightly upwards. Fill most of the tube with pieces of pumice stone or broken porous pot. This will ensure maximum contact time between the ethanol vapour and the hot catalyst. Fit the delivery tube so that it dips into the water in the trough. Fit a Bunsen valve, if desired.
d Heat the pumice stone or porous pot strongly with the tip of medium Bunsen flame for several seconds until thoroughly hot. Avoid heating the tube too close to the rubber stopper. Then flick the flame quickly onto the mineral wool for a few seconds to vaporise some of the ethanol. Then return the flame to the catalyst.
e When a steady stream of gas bubbles is established, collect four to six tubes full of gas by holding them over the Bunsen valve. It is better to have an assistant to manipulate the gas collection tubes, changing and sealing them as they are filled. Take care not to lift the water-filled tubes out of the water when moving them, to avoid letting air into them. Seal the full tubes by pressing them down on the bungs, then place them in a rack.
f Continue with the Bunsen burner heating the mineral wool for about one second out of every ten and the pumice stone for the other nine. To avoid the risk of suck-back, do not remove the Bunsen burner flame from the heated tube while the gas is being collected. If suck-back becomes unavoidable, quickly remove the delivery tube from the water by lifting the whole apparatus using the clamp stand.
g When six tubes of gas have been collected, or gas production ceases, remove the delivery tube from the water by lifting the clamp stand, and then stop heating. Keep the Bunsen flame away from the end of the delivery tube.
h Test the tubes of collected gas as follows:
Pass the first two tubes (mainly air anyway) round the class so that the students can cautiously smell the gas.
Uncork the last tube collected, and hold a lighted spill in its mouth to ignite the gas. It will burn with a yellow flame.
To another test-tube of gas, add about 1 cm depth of bromine water. Re-seal it and shake well. If the pale orange bromine water is decolourised, the gas contains an unsaturated hydrocarbon (a bromoalkanol).
Add about 1 cm depth of acidified potassium permanganate(VII) solution to another test-tube of gas. Re-seal and shake well. If the purple solution is decolorised, possibly leaving a brown coloration of manganese dioxide, the gas contains an unsaturated hydrocarbon (a diol).
The results of the last two tests are characteristic of unsaturated hydrocarbons, whose molecules contain carbon-carbon double bonds.
This experiment would form part of the teaching and learning sequence for the chemistry of hydrocarbons and alcohols. The teacher will need to decide:
how much the students should know about hydrocarbons before this lesson
if they are familiar with hydrocarbons, whether they should be familiar with the potassium manganate(VII) and bromine water tests for a carbon-carbon double bond before the lesson, or should be introduced to these tests by means of this experiment.
For the dehydration of ethanol, the only likely product is ethene. Ball and stick molecular models will be useful for modelling both the dehydration and the tests.
The ethanol dehydration is represented by:
3CH 2OH(g) → CH 2=CH 2(g) + H 2O(g)
The experiment can be linked to the industrial applications of such reactions; see the web-links below.
Bromine in non-aqueous solution adds across the double bond of an alkene, to give for example 1,2-dibromoethane, CH
2Br–CH 2Br (a suspected carcinogen). However, in aqueous solution the main product is a bromoalkanol, such as 2-bromoethanol, CH 2Br–CH 2OH .
Acidified potassium permanganate(VII) acts as an oxidising agent on the double bond to produce diols such as ethan-1,2-diol, CH
2OH–CH 2OH. Under harsher conditions the diols cleave to form two carbonyl compounds (ketones or carboxylic acids).
Industrially some ethanol is made by the reverse reaction, the addition of water to ethene. However, a really important dehydration of an alcohol is the dehydration of 1-phenylethanol to produce phenylethene, better known as styrene, the monomer for polystyrene.
Health & Safety checked, 2016
This Practical Chemistry resource was developed by the Nuffield Foundation and the Royal Society of Chemistry.
© Nuffield Foundation and the Royal Society of Chemistry
A wider review of the dehydration of ethanol and other alcohols to alkenes by various methods:
- discussion of the dehydration of alcohols using aluminium oxide as catalyst
- discussion of the mechanism of this reaction – for A-level and teachers.
Discussion of the manufacture of ethanol from ethene:
- discussion of the manufacture of ethanol
Page last updated October 2015