What are the products of the following reactions, assuming that one equivalent of each reagent is used in each reaction?
c.

Verified step by step guidance

1. Analyze the structure of the starting material: The molecule is a substituted benzene ring with an isopropyl group attached to the aromatic ring. This is known as isopropylbenzene or cumene.
2. Identify the reagent: Chlorine (Cl₂) is used in the reaction, and the absence of light or heat suggests that this is an electrophilic aromatic substitution reaction rather than a free radical halogenation.
3. Understand the mechanism: In electrophilic aromatic substitution, the chlorine molecule reacts with the aromatic ring, and one hydrogen atom is replaced by a chlorine atom. The isopropyl group is an electron-donating group, which activates the aromatic ring and directs substitution to the ortho and para positions relative to the isopropyl group.
4. Predict the products: Since one equivalent of chlorine is used, the reaction will yield a mixture of ortho-chlorocumene and para-chlorocumene as the major products. The meta position is less favored due to the electron-donating effect of the isopropyl group.
5. Consider regioselectivity: The para product is typically favored over the ortho product due to steric hindrance at the ortho position caused by the bulky isopropyl group.

Key Concepts

Conjugated Systems

Conjugated systems consist of alternating single and double bonds, allowing for delocalization of π electrons. This delocalization stabilizes the molecule and can influence its reactivity. In the context of the reaction shown, the conjugated diene can undergo electrophilic addition, where reagents like Cl2 can add across the double bonds.

Electrophilic Addition

Electrophilic addition is a reaction mechanism where an electrophile reacts with a nucleophile, resulting in the addition of atoms or groups to a molecule. In this case, Cl2 acts as an electrophile that adds to the double bonds of the conjugated system, leading to the formation of vicinal dihalides. Understanding this mechanism is crucial for predicting the products of the reaction.

Regioselectivity

Regioselectivity refers to the preference of a chemical reaction to yield one structural isomer over others when multiple possibilities exist. In the reaction with Cl2, the regioselectivity will determine which carbon atoms in the conjugated system will bond with chlorine, influencing the final product's structure. This concept is essential for accurately predicting the outcome of the reaction.