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Reactions of Carboxylic Acids (CIE A Level Chemistry)

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Reactions of Carboxylic Acids to Produce Acyl Chlorides

  • Acyl chlorides are compounds with the functional group -COCl
  • They look similar in structure to carboxylic acids but have a Cl atom instead of an -OH group attached to the carbonyl (C=O)
  • Acyl chlorides are more reactive than their corresponding carboxylic acids and are therefore often used as starting materials in the production of organic compounds such as esters
  • They can be prepared from the reaction of carboxylic acids with:
    • Solid phosphorus(V) chloride (PCl5)
    • Liquid phosphorus(III) chloride (PCl3) and heat
    • Liquid sulfur dichloride oxide (SOCl2)
  • For example, the acyl chloride ethanoyl chloride can be formed from ethanoic acid in the above reactions

Using ethanoic acid to form ethanoyl chloride

Carboxylic Acids & Derivatives - Production of Acyl Chlorides, downloadable AS & A Level Chemistry revision notes

Ethanoic acid can be used to produce ethanoyl chloride with different by-products depending on the reagent used

Further Oxidation of Carboxylic Acids

  • Carboxylic acids can be formed from the oxidation of primary alcohols
  • The primary alcohols are firstly oxidised to aldehydes and then further oxidised to carboxylic acids
  • Some carboxylic acids can get even further oxidised

Methanoic acid

  • Methanoic acid is a strong reducing agent and gets further oxidised to carbon dioxide (CO2)
  • The oxidation of methanoic acid can occur by:
    • Warming methanoic acid with mild oxidising agents such as Fehling’s or Tollens’ reagent
      • In a Fehling’s solution, the Cu2+ ion is reduced to Cu+ ion which precipitates as red Cu2O
      • With Tollens’ reagent, the Ag+ is reduced to Ag
    • Using stronger oxidising agents such as acidified KMnO4 or acidified K2Cr2O7
      • The purple KMnO4 solution turns colourless as Mn7+ ions are reduced to Mn2+ ions
      • The orange K2Cr2O7 solution turns green as the Cr6+ ions are reduced to Cr3+ ions

Ethanedioic acid

  • Another carboxylic acid that can get further oxidised is ethanedioic acid
  • A strong oxidising agent such as warm acidified KMnO4 is required for the oxidation of ethanedioic acid to carbon dioxide

Oxidation of ethanedioic acid

Carboxylic Acids _ Derivatives - Further oxidation of ethanedioic acid, downloadable AS & A Level Chemistry revision notes

Ethanedioic acid is a dicarboxylic acid that can get further oxidised to carbon dioxide

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Caroline

Author: Caroline

Caroline graduated from the University of Nottingham with a degree in Chemistry and Molecular Physics. She spent several years working as an Industrial Chemist in the automotive industry before retraining to teach. Caroline has over 12 years of experience teaching GCSE and A-level chemistry and physics. She is passionate about creating high-quality resources to help students achieve their full potential.