reaction of amines with nitrous acid and reaction of aryl diazonium ions for formation of 2 napthanalgive all 2 steps mechanism of final product REACTION MECHANISMS(Reactions of amines with nitrous acid) ande(Reactions of aryldiazonium ions)Provide the mechanisms (use MarvinSketch, ora similar software) for the tollowing steps:Reaction 1 (formation of nitrosonium ion)Reaction 2 (diazotization of deprotonated sulfanilic acid)Reaction 3 (azo coupling to 2-naphthol)

REACTION MECHANISMS (Reactions of aryl Provide the mechanisms (use MarvinSketch, or (Reactions of amines with nitrous acid) ande diazonium ions). a similar software) for the tollowing steps: Reaction 1 (formation of nitrosonium ion)

REACTION MECHANISMS (Reactions of aryl Provide the mechanisms (use MarvinSketch, or (Reactions of amines with nitrous acid) ande diazonium ions). a similar software) for the tollowing steps: Reaction 1 (formation of nitrosonium ion)

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

Chapter23: Amines

Section23.9: Hofmann Elimination

Problem 23.14P

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Question

reaction of amines with nitrous acid and reaction of aryl diazonium ions for formation of 2 napthanal

give all 2 steps mechanism of final product

REACTION MECHANISMS
(Reactions of amines with nitrous acid) ande
(Reactions of aryl
diazonium ions)
Provide the mechanisms (use MarvinSketch, or
a similar software) for the tollowing steps:
Reaction 1 (formation of nitrosonium ion)
Reaction 2 (diazotization of deprotonated sulfanilic acid)
Reaction 3 (azo coupling to 2-naphthol)

Definition Definition Organic compounds with a nitrogen atom having a lone pair of electrons on it. Amines are derived from ammonia (NH 3 ), wherein hydrogen atoms are substituted by an aryl or alkyl group.

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