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Question 9 (2 points) Which of the following carbocations is (are) likely to undergo rearrangement through a methyl shift? HC
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Answer #1

In ques 9

Option a is correct as because both 1st and 2nd will go 1,2 methyl shift to form tertiary carbocation which is stable due to hyperconjugation.

Where as compound 3 undergoes a 1, 3 methyl shift which is much slower as compared to 1,2 methyl shift. Hence remaing all options are incorrect.

  1. @ ID -) ОС» first. 0 lets see directing effect of och осны och О. ochs,Here attack of che in presence of All is aromatic electrophiftic substitution and from the above mentioned position of attock
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