Which is the correct order of stability of th | vedclass

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(C) In $(I)$ and $(III)$,the positive charge is delocalized through resonance,and the carbocation character is stabilized by the presence of an adjace

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$I \approx III > II$

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(C) In $(I)$ and $(III)$,the positive charge is delocalized through resonance,and the carbocation character is stabilized by the presence of an adjacent alkyl group. Specifically,$(I)$ is a secondary $(2^\circ)$ allylic carbocation,and $(III)$ is a primary $(1^\circ)$ allylic carbocation. However,in $(I)$,the positive charge is on a secondary carbon,while in $(III)$,it is on a primary carbon. In $(II)$,the positive charge is on a primary carbon and is allylic. Comparing the resonance structures and the inductive effects,$(I)$ and $(III)$ show greater stability due to the nature of the allylic system and the electron-donating effects of the methyl group. Thus,the correct order is $(I) \approx (III) > (II)$.

Which is the correct order of stability of the following three carbonium ions?
$(I)$ $CH_2 = CH - CH^+ - CH_3$
$(II)$ $CH_2 = C(CH_3) - CH_2^+$
$(III)$ $CH_3 - CH = CH - CH_2^+$

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Which is the correct order of stability of the following three carbonium ions? $(I)$ $CH_2 = CH - CH^+ - CH_3$ $(II)$ $CH_2 = C(CH_3) - CH_2^+$ $(III)$ $CH_3 - CH = CH - CH_2^+$