Aldehydes?and?ketones?are carbonyl compounds containing a C=O group
They can be prepared from the oxidation of?primary?and?secondary?alcohols?respectively
Oxidising agents
The oxidising agents used to prepare aldehydes and ketones from alcohols include?acidified potassium dichromate?(K2Cr2O7) and?acidified potassium manganate?(KMnO4)
Acidified with dilute sulfuric acid,?potassium dichromate(VI), K2Cr2O7,?is an orange oxidising agent
When the alcohols are?oxidised?the orange dichromate ions (Cr2O72-) are reduced to green Cr3+?ions
Acidified with dilute sulfuric acid,?potassium manganate(VII), KMnO4?is a purple oxidising agent
When the alcohols are?oxidised?the purple manganate ions (MnO4-) are reduced to colourless Mn2+?ions
The oxidising agents change colour when they oxidise an alcohol and get reduced themselves
Synthesis of aldehydes
To make an aldehyde,?warm primary alcohol?is slowly added to the oxidising agent
The formed aldehyde has a lower boiling point than the alcohol and can therefore be?distilled off?as soon as it forms
The aldehyde is then condensed into a liquid and?collected
Aldehydes are formed from the oxidation of primary alcohols
Synthesis of ketones
To make a ketone,?warm secondary alcohol?is slowly added to the oxidising agent
Since the formed?ketone?cannot be further oxidised it does not need to be?distilled off straightaway?after it has been formed
Ketones are formed from the oxidation of secondary alcohols
Exam Tip
If the aldehyde formed is not distilled off, further?refluxing?with excess oxidising agent will oxidise the aldehyde to a?carboxylic acid.
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