Arrange the following compounds in order of increasing reactivity (least reactive first.) to electrophilic aromatic substitution:. Bromobenzene Nitrobenzene Benzene Phenol

a. Bromobenzene < Nitrobenzene < Benzene < Phenol
b. Nitrobenzene < Bromobenzene < Benzene < Phenol
c. Phenol < Benzene < Bromobenzene < Nitrobenzene
d. Nitrobenzene < Benzene < Bromobenzene < Phenol

Nitrobenzene < Bromobenzene < Benzene < Phenol

Explanation:

Aromatic compounds undergo electrophilic aromatic substitution reaction in the presence of relevant electrophiles. Certain substituents tend to increase or decrease the tendency of an aromatic compound towards electrophilic aromatic substitution reaction.

Substituents that increase the electron density around the ring such as in phenol tends to make the ring more reactive towards electrophilic substitution. Halogens such as bromine has a -I inductive effect as well as a +M mesomeric effect.

However the -I(electron withdrawing effect) of the halogens supersedes the +M electron donation due to mesomeric effect.

Putting all these together, the order of increasing reactivity of the compounds towards electrophilic aromatic substitution is;

Nitrobenzene < Bromobenzene < Benzene < Phenol

the product of the pressure and volume is also constant