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Polymers and Life

Acidity of carboxylic acids

  • 2 things to know
  • Components 01, 02 and 03

Overview

Recall questions on why a carboxylic acid is acidic, its reactions with metals, carbonates and alkalis, and why a phenol gives no effervescence.

What you need to know

Answer each one before you reveal it.

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Numbers

What is the equation for ethanoic acid with sodium carbonate, why is the carbonate reaction a useful test for a carboxylic acid, and why does a phenol give no effervescence?

Numbers

Why does magnesium react less vigorously with ethanoic acid than with hydrochloric acid of the same concentration?

Questions from this subtopic

Each one with the model answer underneath.

  1. 1

    Give the formula of the carboxyl functional group.

    Model answer

    The carboxyl group is –COOH.

  2. 2

    Write an equation to show ethanoic acid behaving as an acid in water.

    Model answer

    CH₃COOH ⇌ CH₃COO⁻ + H⁺.

  3. 3

    Why are carboxylic acids described as weak acids?

    Model answer

    Only a small proportion of the molecules release their proton in solution, so the dissociation lies far to the left.

  4. 4

    Name the ion formed when a carboxylic acid loses its proton.

    Model answer

    The carboxylate ion, RCOO⁻.

  5. 5

    Why does the carboxylate ion form more readily than an alkoxide ion from an alcohol?

    Model answer

    The negative charge in the carboxylate ion is spread over both oxygen atoms, which makes the ion more stable and the acid stronger.

  6. 6

    Name the three products formed when a carboxylic acid reacts with a carbonate.

    Model answer

    A carboxylate salt, water and carbon dioxide.

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