Two organic reactions are described below.
Reaction 1: Benzene reacts with bromine in the presence of catalyst to form bromobenzene. The ion is generated as the electrophile, which is attacked by the electrons of the benzene ring.
Reaction 2: Ethyl ethanoate is heated under reflux with dilute hydrochloric acid. The reaction involves nucleophilic attack by water on the carbonyl carbon, followed by loss of ethanol.
Explain why Reaction 1 is classified as an electrophilic substitution reaction and why Reaction 2 is classified as an addition-elimination reaction.