Elimination Reactions of Alcohols (AQA A Level Chemistry): Revision Note
Exam code: 7405
Elimination Reactions
Alcohols can also undergo dehydration to form alkenes
Alcohol vapour is passed over a hot (600 oC) catalyst of aluminium oxide (Al2O3) powder or pieces of porous pot
Excess hot, concentrated sulfuric acid or phosphoric acid is used as a catalyst
Phosphoric(V) acid is used as an alternative dehydrating agent

This is an example of an elimination reaction
Elimination reactions involve a small molecule being formed as a by-product
The water molecule is formed from the -OH group of the alcohol and the H+ from the acid catalyst
The neighbouring hydrogen is then lost as an H+ ion, which regenerates the acid catalyst
The reaction and mechanism for the dehydration of propan-2-ol is shown below

Alkenes produced by this method can be used to produce addition polymers without using monomers derived from crude oil
Related topics
Examiner Tips and Tricks
The most commonly penalised mix-up in this topic: students often confuse this acid-catalysed elimination of water from alcohols with the base-induced elimination of hydrogen halides from halogenoalkanes (drawing an OH⁻ ion attacking a hydrogen). These mechanisms often carry several marks, so it is worth investing the time to practice them.
In this mechanism, any C–H bond that breaks must have the H drawn explicitly — the usual "stick" shorthand (bond drawn without the H) is penalised here even though it's often accepted elsewhere.
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