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(A) $1$. Cyclohexene reacts with $NBS$ followed by $Mg/ether$ to form the Grignard reagent,cyclohex$-2-$en$-1-$ylmagnesium bromide $(A)$.$2$. The Grig

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(A) $1$. Cyclohexene reacts with $NBS$ followed by $Mg/ether$ to form the Grignard reagent,cyclohex$-2-$en$-1-$ylmagnesium bromide $(A)$.$2$. The Grignard reagent $(A)$ reacts with isobutyraldehyde to form an alkoxide,which then undergoes an $S_N2$ reaction with ethyl bromide to form an ether derivative $(B)$.$3$. Finally,the reaction with $OsO_4/H_2O_2$ performs syn-dihydroxylation of the double bond to yield the final product $(C)$.$4$. The syn-addition of two $-OH$ groups to the double bond results in the structure shown in option $(A)$.

Product $(C)$ is

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