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 ▸

In organic chemistry, how can functional groups be easily identified and how can I memorise organic mechanisms?


How does ionic bonding work and what is the structure of an ionic compound?


Why do Copper and Chromium only have 1 electron in their S orbitals?


Why does AlCl3 form the dimer Al2Cl6?