What is the decreasing order of stability for | vedclass

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(D) The correct order of stability is $(ii) > (i) > (iii)$.Step $1$: $(ii)$ $CH_3-CH^{+}-OCH_3$ is the most stable because the lone pair on the oxygen

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

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(D) The correct order of stability is $(ii) > (i) > (iii)$.Step $1$: $(ii)$ $CH_3-CH^{+}-OCH_3$ is the most stable because the lone pair on the oxygen atom provides strong resonance stabilization ($+M$ effect) to the carbocation.Step $2$: $(i)$ $CH_3-CH^{+}-CH_3$ is a secondary carbocation stabilized by hyperconjugation and the inductive effect $(+I)$ of two methyl groups.Step $3$: $(iii)$ $CH_3-CH^{+}-COCH_3$ is the least stable because the carbonyl group $(-COCH_3)$ exerts a strong electron-withdrawing effect ($-I$ and $-M$ effects), which destabilizes the positive charge on the carbon atom.Therefore, the decreasing order is $(ii) > (i) > (iii)$.

What is the decreasing order of stability for the following carbocations?
$(i)$ $CH_3-CH^{+}-CH_3$
$(ii)$ $CH_3-CH^{+}-OCH_3$
$(iii)$ $CH_3-CH^{+}-COCH_3$

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What is the decreasing order of stability for the following carbocations?$(i)$ $CH_3-CH^{+}-CH_3$$(ii)$ $CH_3-CH^{+}-OCH_3$$(iii)$ $CH_3-CH^{+}-COCH_3$