Some pairs of ions are given below. In which pair is the first ion more stable than the second?

  • A
    $CH_3-CH^+-CH_3$ and $CH_3-CH^+-OCH_3$
  • B
    $CH_3-CH_2-CH^+-CH_3$ and $CH_2=CH-CH_2-CH_2^+$
  • C
    Cyclohexylmethyl carbocation and Cyclohex$-1-$enylmethyl carbocation
  • D
    $CH_3-CH(CH_3)-CH_2-C^+(CH_3)_2$ and $CH_3-N(CH_3)-C^+(CH_3)_2$

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Similar Questions

Which of the following carbanions is most stable?

Consider the following compounds:
$(I)$ $(CH_3)_3C-CH^{\bullet}-C_6H_5$
$(II)$ $(C_6H_5)_3C^{\bullet}$
$(III)$ $2$-methylbicyclo$[2.2.1]$hept$-2-$yl radical (as shown in the image)
Hyperconjugation occurs in:

Which free radical structure will show the maximum resonance? (Given: $\phi = C_6H_5$)

Given below are two statements:
Statement $I$: $(CH_3)_3C^{+}$ is more stable than $CH_3^{+}$ as nine hyperconjugation interactions are possible in $(CH_3)_3C^{+}$.
Statement $II$: $CH_3^{+}$ is less stable than $(CH_3)_3C^{+}$ as only three hyperconjugation interactions are possible in $CH_3^{+}$.
In the light of the above statements,choose the correct answer from the options given below.

Identify the most stable free radical from the following.

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