Benzylamine synthesis from benzaldehyde follows the mechanism of reductive amination BECAUSE benzylamine 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 BECAUSE benzylamine 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
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Transcribed Image Text:Benzylamine synthesis from benzaldehyde follows the mechanism of
reductive amination BECAUSE benzylamine 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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