The major product of the following reaction i | vedclass

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(C) The reaction involves the electrophilic addition of $2HBr$ to a conjugated diene system. In the given molecule,the $NO_2$ group is a strong electr

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$3,4-$dibromo$-1-$methyl$-4-$nitrocyclohexane derivative

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(C) The reaction involves the electrophilic addition of $2HBr$ to a conjugated diene system. In the given molecule,the $NO_2$ group is a strong electron-withdrawing group,which deactivates the double bond adjacent to it. The other double bond is more electron-rich and undergoes protonation first to form the most stable carbocation. Following the addition of the first $Br^-$ and then the second $HBr$ molecule,the major product is formed by following Markovnikov's rule and considering the stability of the intermediate carbocation. The final product is $3,4-dibromo-1-methyl-4-nitrocyclohexane$.

The major product of the following reaction is:

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