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(A) The stability of carbocations is determined by the dispersal of positive charge.$(i) \ CH_3^+$ is a methyl carbocation with no electron-donating g

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$(iii) > (ii) > (i)$

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(A) The stability of carbocations is determined by the dispersal of positive charge.$(i) \ CH_3^+$ is a methyl carbocation with no electron-donating groups.$(ii) \ CH_3CH_2^+$ is a primary carbocation stabilized by the $+I$ effect of the methyl group.$(iii) \ CH_3OCH_2^+$ is stabilized by the resonance effect ($+M$ effect) of the oxygen atom,where the lone pair on oxygen donates electron density to the vacant $p$-orbital of the carbocation,making it the most stable.Therefore,the correct order of stability is $(iii) > (ii) > (i)$.

What is the correct order of stability for the given carbocations?
$(i) \ CH_3^+ \quad (ii) \ CH_3CH_2^+ \quad (iii) \ CH_3OCH_2^+$

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What is the correct order of stability for the given carbocations?$(i) \ CH_3^+ \quad (ii) \ CH_3CH_2^+ \quad (iii) \ CH_3OCH_2^+$