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

5680 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

The shape around the oxygen atom in butan-2-ol is non linear. Predict the shape and angle of the C-O-H bond giving explanations


Magnesium is a bulk metal in our bodies. What is it’s main role regarding ATP?


Explain the purpouse of reflux in the oxidation of ethanol to ethanoic acid


What is the difference between a heterogeneous catalyst and a homogeneous 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