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Producing Aldehydes & Ketones (CIE A Level Chemistry)

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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

Carbonyl Compounds Oxidising Agents, downloadable AS & A Level Chemistry revision notes

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

Carbonyl Compounds Synthesis of Aldehydes, downloadable AS & A Level Chemistry revision notes

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

Carbonyl Compounds Synthesis of Ketones, downloadable AS & A Level Chemistry revision notes

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

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Philippa

Author: Philippa

Expertise: Chemistry

Philippa has worked as a GCSE and A level chemistry teacher and tutor for over thirteen years. She studied chemistry and sport science at Loughborough University graduating in 2007 having also completed her PGCE in science. Throughout her time as a teacher she was incharge of a boarding house for five years and coached many teams in a variety of sports. When not producing resources with the chemistry team, Philippa enjoys being active outside with her young family and is a very keen gardener.