Addition of a mineral acid to an olefin bond | vedclass

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(C) The reaction follows the electrophilic addition mechanism,where the rate-determining step is the formation of a carbocation intermediate. In the g

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(C) The reaction follows the electrophilic addition mechanism,where the rate-determining step is the formation of a carbocation intermediate. In the given molecule,there are two double bonds: one in the ring and one in the side chain. The double bond in the side chain is more substituted and its protonation leads to a more stable $3^o$ carbocation compared to the secondary carbocation that would form from the ring double bond. Therefore,the $H^+$ ion adds to the terminal carbon of the side chain to form a $3^o$ carbocation,which is then attacked by the $Br^-$ ion to form the major product.

Addition of a mineral acid to an olefin bond leads to a major product. Identify it.

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