Production of Aldehydes & Ketones
- 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 colour change in common oxidising agents
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
Using distillation to oxidise a primary alcohol to an aldehyde
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
Oxidation of propan-2-ol
Ketones are formed from the oxidation of secondary alcohols
Examiner Tip
If the aldehyde formed is not distilled off, further refluxing with excess oxidising agent will oxidise the aldehyde to a carboxylic acid