Explain the reasons for the changes in reactivity of Phenol, Benzene and MethylBenzene

The changes in reactivity are due to the electron donating/withdrawing properties of the substituted groups. For example the OH group in Phenol is electron donating. This means the electron density of the delocalised ring will have increased, meaning it can polarise bonds more readily. MethylBenzene is less reactive as the Methyl group is electron withdrawing, this means the electron density of the delocalised ring will have decreased, hence decreasing the reactivity. This makes it less reactive than Benzene.

AD
Answered by Adam D. Chemistry tutor

4447 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

By considering the mechanism of the two step reaction of butanone and NaBH4 followed by dilute acid, explain why the product has no effect on plane polarised light.


Calculate the standard enthalpy of combustion of a methane sample by using the standard enthalpies of formation.


Explain, in the context of catalysis, the term heterogeneous and describe the first stage in the mechanism of this type of catalysis.


Explain why silicon dioxide has a higher melting point than sulphur trioxide


We're here to help

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

© MyTutorWeb Ltd 2013–2025

Terms & Conditions|Privacy Policy
Cookie Preferences