Would 4-bromoacetanilide or 4-bromo-2-chloroacetanilide be more reactive toward electrophilic substitution? explain.

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08-08-2018
Chemistry

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Would 4-bromoacetanilide or 4-bromo-2-chloroacetanilide be more reactive toward electrophilic substitution? explain.

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isyllus isyllus · Answer 1 · 2018-08-09T04:35:43+02:00

Answer: -

4-Bromoacetanilide will be more reactive toward electrophilic substitution than 4-bromo-2-chloroacetanilide .

Explanation: -

Electrophilic substitution depends on the electron density of the aromatic ring. More the electron density, more is the reactivity.

Chloro is a electron withdrawing group. So it reduces the electron density of the aromatic benzene ring, thus decreasing the electron density.

Thus, 4-Bromoacetanilide will be more reactive toward electrophilic substitution than 4-bromo-2-chloroacetanilide.

nikitarahangdaleVT nikitarahangdaleVT · Answer 2 · 2022-03-15T17:39:38+01:00

4-bromoacetanilide will be more reactive toward electrophilic substitution reaction as compare to 4-bromo-2-chloroacetanilide.

What is electrophilic substitution reaction?

Those reaction in which substitution is done by the electrophile on the electron rich point.

In the 4-bromo-2-chloroacetanilide, chlorine is present as the substitute which decreases the electron density of the aromatic ring because of the presence of the electron withdrawing chlorine group, as a result chance of the attack of electrophile decreases.

Hence, 4-bromoacetanilide is more reactive towards the electrophile substitution reaction.

To know more about electrophile substitution reaction, visit the below link:

https://brainly.com/question/14525517