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

  • A
    $i > ii > iii > iv$
  • B
    $iv > iii > i > ii$
  • C
    $iv > iii > ii > i$
  • D
    $iii > iv > ii > i$

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Similar Questions

The hybridization of the positively charged carbon and the negatively charged carbon in the following structures are respectively:

The correct order of stability of the given carbocations is:

The compound shown below undergoes racemization on reaction with aqueous acid. Which of the following structures best represents the intermediate responsible for this process?

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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

What is the correct order of stability for $1^\circ, 2^\circ, 3^\circ$ carbocations and benzyl carbocation?

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