Among the given compounds,choose the two that | vedclass

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(C) Upon ionization,compound $A$ ($3$-bromo$-1-$methylcyclohex$-1-$ene) loses a bromide ion to form the $1-$methylcyclohex$-2-$en$-1-$yl cation.Compou

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$A, B$

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(C) Upon ionization,compound $A$ ($3$-bromo$-1-$methylcyclohex$-1-$ene) loses a bromide ion to form the $1-$methylcyclohex$-2-$en$-1-$yl cation.Compound $B$ ($4$-bromo$-1-$methylcyclohex$-1-$ene) loses a bromide ion to form a secondary carbocation at the $C4$ position.This secondary carbocation undergoes a hydride shift to form the more stable allylic $1-$methylcyclohex$-2-$en$-1-$yl cation,which is the same intermediate as formed from compound $A$.Therefore,compounds $A$ and $B$ yield the same carbocation.

Among the given compounds,choose the two that yield the same carbocation on ionization.

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