P methoxybenzyl bromide reacts faster than p nitrobenzyl bromide with

1.	P methoxybenzyl bromide reacts faster than p nitrobenzyl bromide with ethanol
Answer» ANSWER: Explanation: r: METHOXY GROUP is an electron RELEASING group which stabilises the intermediate carbocation. ... Formation of carbocation is the rate DETERMINING step, more the stability of carbocation, faster is the reaction. Hence, p-methoxybenzyl bromide reacts faster than p-nitrobenzyl bromide with ethanol to form ether.

P methoxybenzyl bromide reacts faster than p nitrobenzyl bromide with ethanol

Answer»

Explanation:

r: METHOXY GROUP is an electron RELEASING group which stabilises the intermediate carbocation. ... Formation of carbocation is the rate DETERMINING step, more the stability of carbocation, faster is the reaction. Hence, p-methoxybenzyl bromide reacts faster than p-nitrobenzyl bromide with ethanol to form ether.

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P methoxybenzyl bromide reacts faster than p nitrobenzyl bromide with ethanol

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