What are the products obtained on hydroborati | vedclass

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(C) Hydroboration-oxidation of an alkene is a $syn$-addition reaction where $H$ and $OH$ are added across the double bond in a $syn$ fashion.In the gi

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$II$ and $VI$

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(C) Hydroboration-oxidation of an alkene is a $syn$-addition reaction where $H$ and $OH$ are added across the double bond in a $syn$ fashion.In the given bicyclic alkene ($1$-methylcyclohexene derivative),the $CH_3$ group at the bridgehead position sterically hinders the approach of the borane reagent from the top face.Therefore,the reagent approaches from the less hindered bottom face.This leads to the addition of $H$ and $OH$ from the same side (bottom face) of the double bond.Structure $(II)$ shows $OH$ and $H$ on the bottom face (cis to each other),and structure $(VI)$ shows the same configuration relative to the bridgehead $CH_3$ group.Thus,the products obtained are $(II)$ and $(VI)$.

What are the products obtained on hydroboration-oxidation of the given alkene?

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