Benzylamine synthesis from benzaldehyde follows the mechanism of reductive amination BECAUSEbenzylamine is synthesised form benzaldehyde through an enamine intermediate Hyperconjugation can stabilise carbocation intermediates BECAUSE secbutyl carbocation can rearrange to a tertbutyl carbocation. Reductive amination requires a hydrogen on the carbonyl carbon to proceed BECAUSE Reductive amination converts only aldehydes to amines
Benzylamine synthesis from benzaldehyde follows the mechanism of reductive amination BECAUSEbenzylamine is synthesised form benzaldehyde through an enamine intermediate Hyperconjugation can stabilise carbocation intermediates BECAUSE secbutyl carbocation can rearrange to a tertbutyl carbocation. Reductive amination requires a hydrogen on the carbonyl carbon to proceed BECAUSE Reductive amination converts only aldehydes to amines
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter18: Aromaticity
Section: Chapter Questions
Problem 29CTQ
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Question
The next set of questions are assertion type: There are two statements in a sentence. Choose from the options A-E if
A. Both statements are true and related
B. Both statements are true but not related
C. The first statement is true and the second statement is false
D. The first statement is false and the second statement is true
E. Both statements are false
- Benzylamine synthesis from benzaldehyde follows the mechanism of reductive
amination BECAUSEbenzylamine is synthesised form benzaldehyde through an enamine intermediate - Hyperconjugation can stabilise carbocation intermediates BECAUSE secbutyl carbocation can rearrange to a tertbutyl carbocation.
- Reductive amination requires a hydrogen on the carbonyl carbon to proceed BECAUSE Reductive amination converts only
aldehydes to amines
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