Propene on hydroboration followed by oxidation with alkaline peroxide forms.

  • A
    Tri-$n$-propylborane
  • B
    Tri-isopropylborane
  • C
    Propan-$1$-ol
  • D
    Propan-$2$-ol

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$Ph-CH=CH_2 \xrightarrow[HBr]{(PhCOO)_2} \text{Product}$
Consider the above reaction:
$A$. The reaction proceeds through a more stable radical intermediate.
$B$. The role of peroxide is to generate $\dot{H}$ (Hydrogen radical).
$C$. During this reaction, benzene is formed as a byproduct.
$D$. $1-\text{Bromo}-2-\text{phenylethane}$ is formed as the minor product.
$E$. The same reaction in the absence of peroxide proceeds via a carbocation intermediate.
Identify the correct statements. Choose the correct answer from the options given below:

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