Q.

What is the major product of the following reaction?

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a

b

c

d

answer is D.

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Detailed Solution

The first step is anti addition of Br2 across the double bond. In the second step, EtO- (nu-) gets added by SN1 mechanism and Br- from the dashed position acts as the leaving group leads to the formation of a stable benzylic carbocation.
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