Propan-1-ol Oxidation (Edexcel International A Level Chemistry): Revision Note
Core Practical 7: Oxidation of Propan-1-ol
Oxidation of propan-1-ol
Primary alcohols can be oxidised to form aldehydes which can undergo further oxidation to form carboxylic acids
When propan-1-ol is oxidised, ethanal is produced and when oxidised further propanoic acid will be formed
Synthesis and purification of propanal and propanoic acid
Carefully add 20 cm3 of acidified potassium dichromate(VI) solution, K2Cr2O7 (aq), to a 50 cm3 pear-shaped flask and cool the flask in an iced water bath
Set up the reflux apparatus keeping pear shaped flask cool
Place anti-bumping granules into the pear shaped flask
Measure out 1 cm3 of propan-1-ol
Using a pipette, slowly add the propan-1-ol drop wise into the reflux condenser
When the propan-1-ol has been added remove the ice bath and allow to warm up to room temperature
Position the flask over an electric heater or in a water bath and heat for 20 minutes
Propan-1-ol is flammable, therefore. naked flames should not be used when heating which is why the use of an electric heater or water bath is an important safety precaution
Purify the product using distillation apparatus
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Reflux apparatus for the oxidation of propan-1-ol to propanoic acid
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Oxidation of propan-1-ol by acidified K2Cr2O7 to form propanal by distillation
Hazards, risks and precautions
The alcohols used are flammable and often harmful to health, e.g, propan‐1‐ol, butan‐1‐ol, pentan‐1‐ol
The alcohols should be kept away from naked flames, e.g. a Bunsen burner
Avoid contact with the skin and breathing in the vapour
A fume cupboard can be used for harmful alcohols
Potassium dichromate is a strong oxidising agent and should be handled with care
Spillages should be mopped up right away with plenty of water
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