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
What's in a Medicine?
Esterification and oxidising primary, secondary and tertiary alcohols
- 3 things to know
- Components 01, 02 and 03
Overview
Recall questions on the acid-catalysed ester equilibrium, the dichromate colour change, and what distillation and reflux each give from a primary alcohol.
What you need to know
Answer each one before you reveal it.
What oxidising mixture is used on alcohols, what colour change is seen, and which ion causes the green colour?
What forms when a primary alcohol is refluxed with excess acidified dichromate, and what are the equations using [O]?
Questions from this subtopic
Each one with the model answer underneath.
- 1
What catalyst is used for the esterification of an alcohol with a carboxylic acid?
Model answer
A few drops of concentrated sulfuric acid, or dry hydrogen chloride gas.
- 2
Write the equation for ethanol reacting with ethanoic acid.
Model answer
CH₃COOH + C₂H₅OH ⇌ CH₃COOC₂H₅ + H₂O.
- 3
Why is the equation for esterification written with a reversible arrow?
Model answer
The reaction reaches an equilibrium, because the ester and water can react together in the reverse hydrolysis.
- 4
Give two advantages of using an acid anhydride rather than a carboxylic acid to make an ester.
Model answer
The reaction goes essentially to completion rather than to equilibrium, and it is faster.
- 5
Name the two products formed when ethanol reacts with ethanoic anhydride.
Model answer
Ethyl ethanoate and ethanoic acid are formed.
- 6
State the oxidising mixture used to oxidise alcohols.
Model answer
Potassium dichromate(VI) solution acidified with dilute sulfuric acid is used.
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