(c) (i) Identify the product that would be obtained by the reaction of benzaldehyde (PHCHO) with isopropylamine (Me2CHNH2) under acidic conditions. Draw a full reaction mechanism for its formation. (ii) Explain why piperidine (F) will not react with benzaldehyde in the same way as isopropylamine.

(c) (i) Identify the product that would be obtained by the reaction of benzaldehyde (PHCHO) with isopropylamine (Me2CHNH2) under acidic conditions. Draw a full reaction mechanism for its formation. (ii) Explain why piperidine (F) will not react with benzaldehyde in the same way as isopropylamine.

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter19: Enolate Anions And Enamines

Section: Chapter Questions

Problem 19.63P

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Question

(c) (i)
Identify the product that would be obtained by the reaction of benzaldehyde
(PHCHO) with isopropylamine (Me¿CHNH2) under acidic conditions. Draw a full
reaction mechanism for its formation.
(ii) Explain why piperidine (F) will not react with benzaldehyde in the same way as
isopropylamine.

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