Why is Phenol more reactive than Benzene in electrophilic substitution reactions?

Phenol has the -OH group and the oxygen has a lone pair of electrons which are donated into the Benzene ring and activate the ring which make it more susceptible to attack by electrophiles. This means Phenol can react without an electron carrier catalyst.

Answered by Juliet O. Chemistry tutor

6825 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

The enthalpy of combustion of ethanol is −1371 kJ mol−1 . The density of ethanol is 0.789 g cm−3 . Calculate the heat energy released in kJ when 1 dm3 of ethanol is burned.


What is an empirical formula and how do I calculate it?


Draw an example using a diagram of Carbon, three "Y" substrates and an "L" indicating any leaving group the Sn1 nucleophilic substitution reaction. (3 marks) Which step is fastest (1 mark).


Comparing aluminium and magnesium, which has a lower first ionisation energy? Explain.


We're here to help

contact us iconContact usWhatsapp logoMessage us on Whatsapptelephone icon+44 (0) 203 773 6020
Facebook logoInstagram logoLinkedIn logo
Cookie Preferences