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.

Answered by Romi A. Chemistry tutor

2453 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

Which chemical would have a higher boiling point 1,3-dimethylbutane or hexane


What is the difference between Sn1 and Sn2 reactions?


What is meant by 'activation energy' ?


Describe the enthalpy change of formation of butane.


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