The following reactivity order has been found for the basic hydrolysis of p substituted methyl benzoates Y NO 2 Br H CH 3 OCH 3 How can you explain this reactivity order Where would you expect Y C N Y CHO, and Y NH 2 to he in the reactivity list co 2CH D CH H20

Question: The following reactivity order has been found for the basic hydrolysis of p-substituted methyl benzoates: Y = NO 2 > Br > H > CH

The following reactivity order has been found for the basic hydrolysis of p-substituted methyl benzoates: Y = NO₂ > Br > H > CH₃ > OCH₃. How can you explain this reactivity order? Where would you expect Y = C ? N = Y = CHO, and Y = NH₂ to he in the reactivity list?

co 2CH D CH H20

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