Why is benzene more stable than expected?

All the carbons in benzene are sp2 hybridised. The carbons are each bonded to one hydrogen and all bonds to other carbon atoms in the ring are the same length. This bond is in between the bond length of a C=C and C-C bond. This is because there is a system of p orbitals that can overlap to form a delocalised system of electrons above and below the plane of carbon atoms. This system leads to the benzene ring being more stable than expected.

Related Chemistry A Level answers

All answers ▸

Why does Benzene require a catalyst to react with Bromine whereas Phenol does not?


Which test would you use to identify the difference between an aldehyde and a ketone? Explain your observations.


An iron-alloy nail (2.41g) is dissolved in 100cm3 acid. 10cm3 portions of this solution are titrated with KMnO4 (0.02M) and 9.80cm3 of KMnO4 was needed to react with iron solution. What % of iron by mass is in the nail?


What is the difference between pH and pKa?