Intermediates formed in the reactions $P$ and $Q$ are:
$P: CH_3-CH=CH_2 \xrightarrow{HCl}$
$Q: CH_3-CH=CH_2 \xrightarrow[\text{Peroxide}]{HCl}$

  • A
    $P \to CH_3-CH^{+}CH_3$,$Q \to CH_3-CH(\bullet)-CH_2Br$
  • B
    $P \to CH_3-CH^{+}CH_3$,$Q \to CH_3-CH^{+}CH_3$
  • C
    $P \to CH_3-CH(\bullet)-CH_3$,$Q \to CH_3-CH^{+}CH_2Cl$
  • D
    $P \to CH_3-CH^{+}CH_3$,$Q \to CH_3-CH(\bullet)-CH_2Cl$

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Explain why $((CH_3)_3C)^+$ is more stable than $(CH_3CH_2)^+$ and $(CH_3)^+$ is the least stable carbocation.

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