State and explain the evidence for the delocalisation of electrons in benzene (6 marks)

Benzene does not decolourise bromine water, showing it does not undergo electrophilic addition reactions as the delocalised pi structure is very stable. All of the carbon-carbon bond lengths are the same; the length is intermediate between those expected for carbon-carbon single bonds and carbon-carbon double bonds, showing the electrons are delocalised around the ring.Thermochemically benzene is more stable than the theoretical molecule of cyclohexa-1,3,5-triene due to the added aromatic stability produced by the delocalisation of electrons.

RA
Answered by Romi A. Chemistry tutor

3790 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

What factors affect ionisation energy and how does each of them affect it?


What is electronegativity?


Why does ionisation energy increase across Period 3?


give a possible reaction mechanism for the conversion of a haloalkane to alcohol


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:

© 2025 by IXL Learning