6-156. Arrange the following substituted anilines in increasing order of reactivity toward acetic anhydride: NH2 NH2 NH2 NH2 O₂N. (a) (b) (င) (d) NO2 CI H3C-N CH3
6-156. Arrange the following substituted anilines in increasing order of reactivity toward acetic anhydride: NH2 NH2 NH2 NH2 O₂N. (a) (b) (င) (d) NO2 CI H3C-N CH3
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
Chapter18: Functional Derivatives Of Carboxylic Acids
Section: Chapter Questions
Problem 18.50P
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![X6-156. Arrange the following substituted anilines in increasing order of reactivity toward acetic anhydride:
sllo
NH2
ร้อเป็น
NH2
NH2
edi
NH2
O₂N.
(a)
(b)
----
(c)
(d)
bund
NO2
CI
H3C-N-CH3
Insmiy
X 6-157. Suggest a mechanism for the preparation of acetic anhydride from acetic acid and acetyl chloride in the presence
pyridine (an amine base).](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ffe1a9b0c-96e8-4bc3-9469-9e28a54f7ca5%2Fc3abbfea-7fa1-4941-8f7a-15ebcb93489c%2Fcc89hqm_processed.jpeg&w=3840&q=75)
Transcribed Image Text:X6-156. Arrange the following substituted anilines in increasing order of reactivity toward acetic anhydride:
sllo
NH2
ร้อเป็น
NH2
NH2
edi
NH2
O₂N.
(a)
(b)
----
(c)
(d)
bund
NO2
CI
H3C-N-CH3
Insmiy
X 6-157. Suggest a mechanism for the preparation of acetic anhydride from acetic acid and acetyl chloride in the presence
pyridine (an amine base).
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