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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Chapter1: Chemical Foundations
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State whether the following statements are true or false or related

1

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
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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