Addition of BH_3 followed by H_2O_2 to trans- | vedclass

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(B) The reaction of $trans-2-butene$ with $BH_3$ followed by $H_2O_2/OH^-$ is a hydroboration-oxidation process,which proceeds via $syn-addition$. Whe

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racemic

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(B) The reaction of $trans-2-butene$ with $BH_3$ followed by $H_2O_2/OH^-$ is a hydroboration-oxidation process,which proceeds via $syn-addition$. When $syn-addition$ of $OH$ and $H$ occurs across the double bond of $trans-2-butene$,it results in the formation of $butan-2-ol$. Since the product $butan-2-ol$ has a chiral center,the reaction produces a pair of enantiomers in equal amounts,resulting in a $racemic$ mixture.

Addition of $BH_3$ followed by $H_2O_2$ to $trans-2-butene$ would give a product which is

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