18. Reactions of Aromatics:EAS and Beyond
Electron Withdrawing Groups
38PRACTICE PROBLEM
Iodination of ethylbenzene follows electrophilic aromatic substitution. In the second step of this reaction, water acts as a base and removes a proton from the sigma complex. Show the product you would expect if the water would act as a nucleophile instead of a base. Explain why this reaction is not feasible.
Iodination of ethylbenzene follows electrophilic aromatic substitution. In the second step of this reaction, water acts as a base and removes a proton from the sigma complex. Show the product you would expect if the water would act as a nucleophile instead of a base. Explain why this reaction is not feasible.