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

Related Chemistry A Level answers

All answers ▸

At what temperature would 0.05 moles of nitrogen gas occupy 1000cm^3 at 50kPa?


3-Methylpent-2-ene (CH3CH=C(CH3)CH2CH3) reacts with Hydrogen Chloride(HCl) forming a major and minor product. Please name the reaction, draw the mechanism for the formation of the major product and briefly explain why there is a major and a minor product.


The ratio between the molar mass of an alkene(A) and an alkyne(B) with the same number of carbon atoms is 1.05. Find the molecular formulas of the two hydrocarbons then write the reaction for how we can obtain the alkene A from the alkyne B.


X, a gas, has a mass of 0.270g and is present in a gas syringe with a volume of 105.0cm^3 at 97C and 100kPa. Calculate the Mr of X. (5 marks)