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

2745 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

Describe how you could form ethyl ethanoate using only ethanol as the starting material. Include all relevant reagents and conditions.


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


Why is the first ionisation energy of Potassium less than Sodium?


What is a chiral carbon?


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