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.

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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.
Transcribed Image Text: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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