Draw the major product for the reaction of benzene with the given reagents below.

(i) 2-bromo-2-methylbutane, AlCl₃

(ii) 1-chloropropane, AlCl₃

Identify the major product of the reaction:

Write the mechanism for the reaction shown below.

What major product is expected from the reaction shown below?

Propose the synthesis that would produce (cyclohexylmethyl)benzene using the Friedel-Crafts acylation, Clemmensen reduction, or Gatterman-Koch reaction.

Write the correct synthetic sequence for preparation of the following compound using Friedel–Crafts acylation and/or Clemmensen reduction.

In electrophilic aromatic substitution reactions, which of the following positions on the benzene ring are typically activated by electron-donating groups?

Why does the ortho position have a numerical advantage in EAS reactions compared to the para position?

Under what condition is the para position favored over the ortho position in an EAS reaction?

Friedel–Crafts alkylation suffers from overalkylation.

i. Identify the product of the reaction below considering overalkylation

ii. What makes it difficult to control and add only one alkyl group?

Propose the products formed by the light-induced reaction of the following compounds with (i) 1 equivalent of bromine and (ii) excess of bromine.

a. Toluene

b.

Determine the product of the reaction between the given compound and H₂CrO₄ + Δ.

Give the product of the reaction given below:

What major product is expected from the reaction shown below?