Question: Hydroborationoxidation of pinene (page 213), like catalytic hydrogenation, is stereoselective. Addition takes place at the less hindered face of the double bond, and a single

Hydroboration–oxidation of pinene (page 213), like catalytic hydrogenation, is stereoselective. Addition takes place at the less hindered face of the double bond, and a single alcohol is produced in high yield (89%). Suggest a reasonable structure this alcohol.

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