Explain why phenol is nitrated more readily than benzene.

  1. Phenol has a lone pair of electrons on the O group which can be delocalised into the benzene Pi system2) This delocalisation increases the electron density in the pi system compared to benzene3) This increase makes phenol more susceptible to electrophilic attack
DB
Answered by Daniel B. Chemistry tutor

3473 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

24.5g of CH3CH2CH2Br was reacted with ammonia to form CH3CH2CH2NH2 at a 75.0% yield, calculate the mass of the product formed.


How does hydrogen bonding work?


Sort the following compounds in order of increasing boiling point and explain your reasoning: hydrogen, hydrogen fluoride and hydrogen bromide


Why does phenol readily undergo electrophilic substitution but benzene does not without the aid of a catalyst?


We're here to help

contact us iconContact ustelephone icon+44 (0) 203 773 6020
Facebook logoInstagram logoLinkedIn logo

MyTutor is part of the IXL family of brands:

© 2026 by IXL Learning