Arrange the compounds by their reactivity toward electrophilic aromatic substitution. a. Benzene, ethylbenzene, chlorobenzene, nitrobenzene, anisole.
b. Toluene, p-cresol, benzene, p-xylene.
c. Benzene, benzoic acid, phenol, propylbenzene.
d. p-Methylnitrobenzene, 2-chloro-1-methyl-4-nitrobenzene, 1-methyl-2,4-dinitrobenzene, p-chloromethylbenzene.

The order of reactivity towards electrophilic susbtitution is shown below:

a. anisole > ethylbenzene>benzene>chlorobenzene>nitrobenzene

b. p-cresol>p-xylene>toluene>benzene

c.Phenol>propylbenzene>benzene>benzoic acid

d.p-chloromethylbenzene>p-methylnitrobenzene> 2-chloro-1-methyl-4-nitrobenzene> 1-methyl-2,4-dinitrobenzene

Explanation:

Electron donating groups favor the electrophilic substitution reactions at ortho and para positions of the benzene ring.

For example: -OH, -OCH3, -NH2, Alkyl groups favor electrophilic aromatic substitution in benzene.

The -I (negative inductive effect) groups, electron-withdrawing groups deactivate the benzene ring towards electrophilic aromatic substitution.

Examples: -NO2, -SO3H, halide groups, Carboxylic acid groups, carbonyl gropus.

the mass of the cathode increases because ions from the solution get reduced to atoms and become part of the cathode.

explanation:

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