What is the mechanism of the following reaction? EN : Nu Nu №₂ A two-step mechanism involving the formation of a benzyne intermediate A multistep mechanism involving bonding of nucleophile to -N: (+), followed by rearrangement, then loss of N₂ leaving group. O S 2 mechanism, where Nu:(-) replaces -N₂ leaving group in a single step CI A two-step process, where a 6-member ring carbanion intermediate is formed in first step. followed by ejection of CI(-) in second step. O An S1 mechanism in which the diazonium ion forms a phenyl cation in the first step (N, is leaving group), followed by attachment of Nu:(-) to the benzene ring.

What is the mechanism of the following reaction? EN : Nu Nu №₂ A two-step mechanism involving the formation of a benzyne intermediate A multistep mechanism involving bonding of nucleophile to -N: (+), followed by rearrangement, then loss of N₂ leaving group. O S 2 mechanism, where Nu:(-) replaces -N₂ leaving group in a single step CI A two-step process, where a 6-member ring carbanion intermediate is formed in first step. followed by ejection of CI(-) in second step. O An S1 mechanism in which the diazonium ion forms a phenyl cation in the first step (N, is leaving group), followed by attachment of Nu:(-) to the benzene ring.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 38MP: Benzenediazonium carboxylate decomposes when heated to yield N2, CO2, and a reactive substance that...

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