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

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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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

  1. Benzylamine synthesis from benzaldehyde follows the mechanism of reductive amination BECAUSEbenzylamine is synthesised form benzaldehyde through an enamine intermediate
  2. Hyperconjugation can stabilise carbocation intermediates BECAUSE secbutyl carbocation can rearrange to a tertbutyl carbocation.
  3. Reductive amination requires a hydrogen on the carbonyl carbon to proceed BECAUSE Reductive amination converts only aldehydes to amines
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