What is the mechanism of the following reaction? CI EN : Nu Nu + N₂ + CI A two-step mechanism involving the formation of a benzyne intermediate A multistep mechanism involving bonding of nucleophile to -N₂ (+), followed by rearrangement, then loss of N₂ leaving group. x A two-step process, where a 6-member ring carbanion intermediate is formed in first step, followed by ejection of CI(-) in second step. SN2 mechanism, where Nu:(-) replaces -N₂ leaving group in a single step An SN1 mechanism in which the diazonium ion forms a phenyl cation in the first step (N₂ is leaving group), followed by attachment of Nu:(-) to the benzene ring.

What is the mechanism of the following reaction? CI EN : Nu Nu + N₂ + CI A two-step mechanism involving the formation of a benzyne intermediate A multistep mechanism involving bonding of nucleophile to -N₂ (+), followed by rearrangement, then loss of N₂ leaving group. x A two-step process, where a 6-member ring carbanion intermediate is formed in first step, followed by ejection of CI(-) in second step. SN2 mechanism, where Nu:(-) replaces -N₂ leaving group in a single step An SN1 mechanism in which the diazonium ion forms a phenyl cation in the first step (N₂ 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 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...

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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. 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 S2 mechanism, where Nu:(-) replaces-N₂ leaving group in a single 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.
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