Arrange the following carbocations in decreas | vedclass

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(D) The stability of carbocations is determined by factors like resonance and inductive effect.$I$ is an ethyl carbocation $(CH_3-CH_2^+)$,which is a

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$III > II > I$

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(D) The stability of carbocations is determined by factors like resonance and inductive effect.$I$ is an ethyl carbocation $(CH_3-CH_2^+)$,which is a primary $(1^{\circ})$ carbocation stabilized only by the inductive effect of one methyl group.$II$ is an isopropyl carbocation $((CH_3)_2CH^+)$,which is a secondary $(2^{\circ})$ carbocation stabilized by the inductive effect and hyperconjugation of two methyl groups.$III$ is a benzyl carbocation $(Ph-CH_2^+)$,which is highly stabilized by resonance with the phenyl ring.Comparing their stabilities: Resonance stabilization in $III$ makes it the most stable. Between $I$ and $II$,the secondary carbocation $II$ is more stable than the primary carbocation $I$ due to more hyperconjugation and inductive effect.Therefore,the decreasing order of stability is $III > II > I$.

Arrange the following carbocations in decreasing order of stability:
$I: CH_3-CH_2^+$
$II: (CH_3)_2CH^+$
$III: Ph-CH_2^+$

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Arrange the following carbocations in decreasing order of stability:$I: CH_3-CH_2^+$$II: (CH_3)_2CH^+$$III: Ph-CH_2^+$