Carboxylic Acids (AQA A Level Chemistry): Revision Note

Exam code: 7405

Stewart Hird

Written by: Stewart Hird

Reviewed by: Caroline Carroll

Updated on

Carboxylic Acids

Carboxylic acids

  • Carboxylic acid is the name given to the family of compounds that contain the carboxyl functional group, -COOH

  • The general formula of a carboxylic acid is CnH2n+1COOH which can be shortened to just RCOOH

    • (In some countries, this family is also called alkanoic acid)

  • The nomenclature of carboxylic acid follows the pattern alkan + oic acid, e.g. propanoic acid

  • There is no need to use numbers in the name as the carboxyl group, COOH, is always on the number 1 carbon atom

Carboxylic Acids Examples Table

Carboxylic Acids Examples Table, downloadable AS & A Level Chemistry revision notes

Weak Acids

  • Carboxylic acids with fewer than six carbon atoms per molecule are water-soluble

    • This is because water molecules can hydrogen-bond with the functional group

  • In aqueous solution they are only slightly ionised, to give low concentrations of hydronium ions and alkanoate ions (often called carboxylate ions)

Weak acids, downloadable AS & A Level Chemistry revision notes

Carboxylic acids are weak acids that do not fully dissociate in water, the position of the equilibrium lies to the left

  • This partial ionisation in solution means that carboxylic acids are weak acids

  • This means that the position of the equilibrium lies to the left and that the concentration of H+ is much smaller than the concentration of the carboxylic acid

  • However, the concentration of hydrogen ions is sufficient to react with an aqueous solution of sodium carbonate or sodium hydrogen carbonate to produce carbon dioxide

  • These reactions are a useful test for the possible presence of a carboxylic acid:

    • Sodium carbonate: 2RCOOH + Na2CO3 → 2RCOO-Na+ CO2 + H2O

    • Ionic equation with carbonates: 2RCOOH + CO32- → 2RCOO- + CO2 + H2O

    • Sodium hydrogen carbonate: RCOOH + NaHCO3 → RCOO-Na+ + CO2 + H2O

    • Ionic equation with hydrogen carbonates: RCOOH + HCO3- → RCOO- + CO2 + H2O

Preparation of esters

  • Esters are formed from the condensation reaction between an alcohol and carboxylic acid in the presence of a concentrated strong acid catalyst e.g. sulfuric or hydrochloric acid

  • This reaction is often referred to as esterification

  • A condensation reaction involves the elimination of a small molecule not always water

    • Esterification is one example of a condensation reaction as water is eliminated from the acid and alcohol reacting together

Hydroxy Compounds Esterification of Alcohols, downloadable AS & A Level Chemistry revision notes

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Stewart Hird

Author: Stewart Hird

Expertise: Chemistry Content Creator

Stewart has been an enthusiastic GCSE, IGCSE, A Level and IB teacher for more than 30 years in the UK as well as overseas, and has also been an examiner for IB and A Level. As a long-standing Head of Science, Stewart brings a wealth of experience to creating Topic Questions and revision materials for Save My Exams. Stewart specialises in Chemistry, but has also taught Physics and Environmental Systems and Societies.

Caroline Carroll

Reviewer: Caroline Carroll

Expertise: Head of Content Delivery

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 delivering high-quality resources to help students achieve their full potential.