AQA A-Level Chemistry 7405
Atomic Structure
Amount of Substance
Bonding
Energetics and Thermodynamics
Kinetics
Chemical Equilibria
Redox and Electrochemistry
Acids and Bases
Periodicity and Group Chemistry
Period 3 Elements and Their Oxides
Transition Metals
Introduction to Organic Chemistry
Hydrocarbons
Halogenoalkanes, Alcohols and Organic Analysis
Carbonyls, Carboxylic Acids and Derivatives
Aromatic Chemistry and Amines
Polymers, Amino Acids, Proteins and DNA
Organic Synthesis, NMR and Chromatography
Carbonyls, Carboxylic Acids and Derivatives
Reduction of Carbonyls with NaBH4
- 3 things to know
- Papers 2 and 3
Overview
Reduction to primary and secondary alcohols, and the nucleophilic addition mechanism.
What you need to know
Answer each one before you reveal it.
What type of product is formed when an aldehyde is reduced with NaBH₄?
What type of product is formed when a ketone is reduced with NaBH₄?
Questions from this subtopic
Each one with the model answer underneath.
- 1
What reducing agent is used to reduce aldehydes and ketones to alcohols?
Model answer
Sodium borohydride (NaBH₄)
- 2
What type of product is formed when an aldehyde is reduced with NaBH₄?
Model answer
A primary alcohol
- 3
What type of product is formed when a ketone is reduced with NaBH₄?
Model answer
A secondary alcohol
- 4
What type of reaction mechanism occurs when NaBH₄ reduces a carbonyl compound?
Model answer
Nucleophilic addition
- 5
In the nucleophilic addition mechanism with NaBH₄, which species acts as the nucleophile?
Model answer
The hydride ion (H⁻)
- 6
Which atom in the carbonyl group does the hydride ion attack during reduction with NaBH₄?
Model answer
The carbonyl carbon atom
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