The order of stability of the following carbocations is:
$I$. $CH_2 = CH - CH_2^+$
$II$. $CH_3 - CH_2 - CH_2^+$
$III$. $C_6H_5CH_2^+$

  • A
    $III > I > II$
  • B
    $I > II > III$
  • C
    $II > III > I$
  • D
    $III > II > I$

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Similar Questions

Based upon an understanding of product stability,predict the product formed when the following dianion reacts with one equivalent of acid $(H^+)$.

What is the decreasing order of stability for the following carbocations?
$(i)$ $CH_3-CH^{+}-CH_3$
$(ii)$ $CH_3-CH^{+}-OCH_3$
$(iii)$ $CH_3-CH^{+}-COCH_3$

Which of the following is the most stable free radical?

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The most stable carbocation is

Which of the following represents the incorrect order of stability?

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