of the following reactions is a Nucleophilic Aromatic Substitution reaction? A. When 2,4-dinitrochlorobenzene is heated with NaOH/H₂0, 2,4-dinitrophenol is formed. B. Bromobenzene is converted to aniline when treated with K*NH₂ in liquid NH³. C. Phenyl diazonium bromide is converted to iodobenzene when treated with KI D. All of the above reactions.

How do you write out the reactions (reactants, conditions and products) for the following electrophilic aromatic substitution reactions   Bromination of methylbenzoate             Nitration of anisole (methoxybenzene) Bromination of anisole (methoxybenzene)

What is the role of the catalyst in electrophilic aromatic substitution reactions of benzene? O a. The catalyst reacts with the non-benzene reactant to form the electrophile in the reaction. O b. The catalyst speeds up the reaction by e deprotonating the arenium ion that forms in the reaction. O c. The catalyst attaches to the benzene ring, making it more susceptible to electrophilic substitution O d. The catalyst prevents addition reaction from occurring. Give the organic product(s) :0 O hp US Mar 29 10:56