Why is phenol nitrated more readily than benzene

The electron density in the phenol ring is higher than that of the benzene ring due to the presence of the OH group. This allows the electron substitution reaction to happen without a sulphuric acid catalyst.

Related Chemistry A Level answers

All answers ▸

What is the electronic configuration of Chlorine and of a chloride ion and explain why Chlorine is 'happiest' as a chloride ion.


How to calculate acidic buffer solution pH, and how do they behave?


Explain why sulfur deviates from the general trend in ionisation energies across period 3.


Why does Benzene require a catalyst to react with Bromine whereas Phenol does not?