Question

Arrange the following in decreasing order of stability of following reaction intermediates (along with explanation)

Answer 1

Answer:

The methyl group shows inductive effect only which is distance dependent so here order should be 3>2>1

Thanks for asking

Answer 2

Answer:

Explanation:

The correct answer is III>I>II

since the ortho position stabilises the +ve charge immediately

and the para position stabilises the +ve charge after sometime

(both stabilisation takes place directly at both the positions, please draw the resonance structures, or you can ask me or surf the net)

The meta position has a very less possibility of stabilisin the positive charge.......

that's why this order.........

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