The product of the rearrangement of the given | vedclass

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(D) The given species is an oxyallyl cation. The rearrangement involves the nucleophilic attack of the negatively charged oxygen atom on the positivel

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(D) The given species is an oxyallyl cation. The rearrangement involves the nucleophilic attack of the negatively charged oxygen atom on the positively charged carbon atom,leading to the formation of a three-membered ring containing a carbonyl group (cyclopropanone derivative). The mechanism proceeds via the internal cyclization of the oxyallyl intermediate to form a cyclopropanone ring attached to the benzene ring substituted with an $OMe$ group.

The product of the rearrangement of the given oxyallyl cation is:

Similar Questions

Which of the following carbanions is the least stable?

Which of the following is the most stable form for the given structure after rearrangement?

Write structures of various carbocations that can be obtained from $2-$methylbutane. Arrange these carbocations in order of increasing stability.

The order of stability of carbonium ions is:

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