(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
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter11: Reactions Of Alkyl Halides: Nucleophilic Substitutions And Eliminations
Section11.SE: Something Extra
Problem 35MP: One step in the urea cycle for ridding the body of ammonia is the conversion of argininosuccinate to...
icon
Related questions
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.
Transcribed Image Text:(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.
Expert Solution
steps

Step by step

Solved in 2 steps with 2 images

Blurred answer
Knowledge Booster
Carboxylic Acids and their Derivatives
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9781305080485
Author:
John E. McMurry
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9781305580350
Author:
William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:
Cengage Learning