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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Similar Questions

Stability order of the following carbocations is:
$(i)$ $CH_3-C^{+}(CH_3)-CH_2-CH_3$
$(ii)$ $CH_3-CH^{+}-CH_3$
$(iii)$ $CH_3-C^{+}(CH_3)-CH_3$
$(iv)$ $Ph-CH^{+}-CH_3$

The correct order of stability of the given carbanions is:

Arrange the following anions in decreasing order of their stability:
$CH_3^{\Theta}, NH_2^{\Theta}, OH^{\Theta}, Cl^{\Theta}$

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Among the following, which is the most stable carbocation?

Determine the decreasing order of stability for the following carbocations: $(I) \ CH_3-C^+(CH_3)-CH_3$,$(II) \ CH_3-CH^+(OCH_3)$,$(III) \ CH_3-CH^+(COCH_3)$.

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