The correct stability order of the following carbocations is:
$I$. $H_2C^+-CH=CH-CH_3$
$II$. $H_2C^+-CH=CH-BMe_2$
$III$. $H_2C^+-CH=CH-NMe_2$
$IV$. $H_2C^+-CH=CH-OMe$

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

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Similar Questions

What is the correct order of stability for the given carbocations?
$(i) \ CH_3^+ \quad (ii) \ CH_3CH_2^+ \quad (iii) \ CH_3OCH_2^+$

Match the intermediates given in Column $-I$ with their probable structure in Column $-II$.
Column $-I$ Column $-II$
$A$. Free radical $1$. Trigonal planar
$B$. Carbocation $2$. Pyramidal
$C$. Carbanion $3$. Linear

Which of the following has an unstable enol form?

Difficult
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$CH_3-C(CH_3)_2-CH_2-CH_2^+ \to CH_3-C^+(CH_3)-CH(CH_3)-CH_3$
How many $H^-$ shifts are involved in the above rearrangement?

Which of the following carbocations is the most stable?

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