Why is a benzene ring so stable (3 marks)?

The p orbitals on each carbon atom in benzene overlapThere is delocalisation of electrons in the ring (not 3 localised C==C double bonds)This makes benzene more thermodynamically stable than predictedIt therefore undergoes substitution reactions rather than addition reactions because addition reaction break the delocalisation in the ring. e.g The nitration of benzene results in a loss of H+ which is replaced by NO2+

AC

Related Chemistry A Level answers

All answers ▸

A) The compound butan-2-ol reacts with acidified potassium dichromate(VI) to form a new compound. Give the IUPAC name of the Product. B) 2,2-dimethyl butan-2-ol was subjected to the same conditions. State and explain the outcome


Why is the Harber process performed at higher temperatures rather than low?


Draw the reaction mechanism for the formation of ethanol from bromoethane and water and name the mechanism.


Explain the shape carbon tetrachloride