Draw a structural formula for the alkene you would use to prepare the alcohol shown by hydroboration/oxidation.

See explanation

Explanation:

The question is incomplete because the image of the alcohol is missing. However, I will try give you a general picture of the reaction known as hydroboration of alkenes.

This reaction occurs in two steps. In the first step, -BH2 and H add to the same face of the double bond (syn addition).

In the second step, alkaline hydrogen peroxide is added and the alcohol is formed.

Note that the BH2 and H adds to the two atoms of the double bond. The final product of the reaction appears as if water was added to the original alkene following an anti-Markovnikov mechanism.

Steric hindrance is known to play a major role in this reaction as good yield of the anti-Markovnikov like product is obtained with alkenes having one of the carbon atoms of the double bond significantly hindered.

answer; ///(u-235); ///is the correct

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explanation:

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