The most stable carbocation among the following is:

  • A
    $(CH_{3})_{3}C^{+}$
  • B
    $CH_{3}CH_{2}CH^{+}CH_{2}CH_{3}$
  • C
    $CH_{3}CH^{+}CH_{2}CH_{2}CH_{3}$
  • D
    $CH_{3}CH_{2}CH_{2}^{+}$

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Similar Questions

Arrange the following carbanions in the decreasing order of stability:
$I. \ p-Br-C_6H_4-CH_2^-$
$II. \ C_6H_5-CH_2^-$
$III. \ p-CH_3O-C_6H_4-CH_2^-$
$IV. \ p-CHO-C_6H_4-CH_2^-$
$V. \ p-CH_3-C_6H_4-CH_2^-$
Choose the correct answer from the options given below:

Among the given species,which carbocations are resonance stabilized?

Which of the following carbanions is the least stable?

Arrange the following cations in decreasing order of their stability:
$(a)$ $CH_3^+$
$(b)$ $F-CH_2-CH_2^+$
$(c)$ $Br-CH_2-CH_2^+$
$(d)$ $CH_3-CH_2-CH_2^+$

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The correct order of relative stability for the given free radicals is:

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