Which carbocation is the least stable?

  • A
    $H_3C^+$
  • B
    $(CH_3)_3C^+$
  • C
    $(CH_3)_2CH^+$
  • D
    $CH_2=CH-CH_2^+$

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Similar Questions

The stability of carbanions follows the order:
$I: CH_3CH_2CH_2\bar{C}H_2$
$II: CH_3\bar{C}HCH_2CH_3$
$III: (CH_3)_3\bar{C}$
$IV: CH_3\bar{C}(Ph)CH_2CH_3$

The stability order of the following carbocations is:

Match the following columns and select the correct option.
List-$I$ (Carbocation) List-$II$ (Type)
$A$. $CH_3-C^{+}(CH_3)-CH_3$ $I$. Secondary carbocation
$B$. $CH_3-C^{+}H-CH_3$ $II$. Methyl carbocation
$C$. $CH_3-CH_2^+$ $III$. Primary carbocation
$D$. $CH_3^+$ $IV$. Tertiary carbocation

Which of the following carbocations is the most stable?

Most stable carbocation is

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