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Carboxylic acids

The form a . Like all homologous series, the carboxylic acids:

  • have the same
  • differ by CH2 in from neighbouring
  • show a gradual variation in physical , such as their
  • have similar chemical properties

Functional group

The in the carboxylic acids is the group, -COOH. It is responsible for the typical reactions of carboxylic acids, which are weak . Vinegar is a dilute of ethanoic acid.

Structures

The table shows four carboxylic acids, their molecular formulae and their structures.

Table of four carboxylic acids; methanoic acid, ethanoic acid, propanoic acid and butanoic acid, with their formula and structures.

Acid properties

The carboxylic acids have the typical properties of acids. For example, they:

  • in water to form with values less than 7
  • react with to form a and hydrogen
  • react with to form a salt and water
  • react with carbonates to form a salt, water and carbon dioxide

These properties are due to the –COOH functional group.

Making esters

Carboxylic acids can react with alcohols to make . Esters are which all contain the -COO-. Esters have fruity smells and can be used as .

The general equation for the formation of an ester is:

alcohol + carboxylic acid → ester + water

For example:

ethanol + ethanoic acid → ethyl ethanoate + water

Ethanol and ethanoic acid combine to form ethyl ethanoate and water.

Weak and strong acids - Higher

Carboxylic acids are weak acids. This means that their solutions do not contain many hydrogen ions compared with a solution of a strong acid with the same . The pH of a weak acid will be higher than the pH of a strong acid, if their concentrations are the same.

In a solution of a strong acid, the molecules are fully ionised, but in a weak acid, very few of the molecules are .