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(C) $1$. Cyclohexene reacts with $NBS$ followed by $Mg/ether$ to form cyclohex$-2-$en$-1-$ylmagnesium bromide.$2$. This Grignard reagent reacts with i

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(C) $1$. Cyclohexene reacts with $NBS$ followed by $Mg/ether$ to form cyclohex$-2-$en$-1-$ylmagnesium bromide.$2$. This Grignard reagent reacts with isobutyraldehyde to form an alkoxide,which is then alkylated with ethyl bromide $(CH_3CH_2Br)$ to form an ether derivative of cyclohexenol.$3$. Finally,the reaction with $OsO_4/H_2O_2$ performs syn-dihydroxylation of the double bond,resulting in the product shown in the solution image.

Product $(C)$ is

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