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

1809 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

How does the 3D dash and wedge notation work?


Why is benzene more stable than expected?


Chlorine, 15 g, is contained in a vessel with a volume of 0.80 dm3 at 330 K. Calculate the pressure exerted when the chlorine is treated as a perfect (ideal) gas giving your answer in terms of kPa


What is Hund's rule?


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 2013–2024

Terms & Conditions|Privacy Policy