$A$ hydrocarbon having molecular formula $C_5H_{10}$ produced a tertiary alcohol upon treatment with a few drops of conc. sulphuric acid and water. The same hydrocarbon when reacted with acidic potassium permanganate produced a ketone and a carboxylic acid. The hydrocarbon is $....$

  • A
    cyclopentane
  • B
    $1$-pentene
  • C
    $2$-methyl$-2$-butene
  • D
    $2$-pentene

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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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