Chapter 11

Carboxylic Acids

Carboxylic acids contain -COOH and are weak acids; see how ethanoic acid reacts with metals, carbonates, alkalis and alcohols.

The carboxylic acid family

Carboxylic acids are a homologous series with the general formula CnH2n+1COOH. Every member contains the carboxyl functional group, -COOH. The most important example is ethanoic acid, CH3COOH, the acid in vinegar. Methanoic acid (HCOOH) is the first member.

Key idea / 要点

Functional group: -COOH (carboxyl). Carboxylic acids are weak acids: in water they are only partially ionised, so they have a lower H+ concentration than a strong acid of the same concentration.

Typical acid reactions

Although weak, carboxylic acids show all the usual acid reactions:

  • With a reactive metal → salt + hydrogen. e.g. magnesium gives magnesium ethanoate + H2.
  • With a carbonate → salt + water + carbon dioxide (fizzing).
  • With an alkali (neutralisation) → salt + water, e.g. NaOH gives sodium ethanoate + water.

The salts are named after the acid: ethanoic acid forms ethanoates. Carboxylic acids can be made by oxidising alcohols (ethanol → ethanoic acid). They also react with alcohols, in the presence of an acid catalyst, to form sweet-smelling esters plus water.

Worked example / 例题

Find the relative molecular mass of ethanoic acid, CH3COOH (Ar: H=1, C=12, O=16). It contains 2C, 4H and 2O: (2×12) + (4×1) + (2×16) = 24 + 4 + 32 = 60.

Remember / 记住

  • -COOH is the carboxyl group; acids are weak (partly ionised).
  • acid + carbonate → salt + water + CO2.
  • acid + alcohol → ester + water.

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