OCR A-Level Chemistry B H433
Development of Practical Skills in Chemistry
Elements of Life
Developing Fuels
Elements From the Sea
The Ozone Story
What's in a Medicine?
The Chemical Industry
Polymers and Life
Oceans
Developing Metals
Colour by Design
Chemical Literacy
Mathematical Skills in Chemistry
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.
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
Give the formula of the carboxyl functional group.
Model answer
The carboxyl group is –COOH.
- 2
Write an equation to show ethanoic acid behaving as an acid in water.
Model answer
CH₃COOH ⇌ CH₃COO⁻ + H⁺.
- 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
Name the ion formed when a carboxylic acid loses its proton.
Model answer
The carboxylate ion, RCOO⁻.
- 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
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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