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Chapter1: Chemical Foundations
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### Reaction Overview

The image depicts a chemical reaction where benzene reacts with benzoyl chloride in the presence of aluminum chloride (AlCl₃) as a catalyst. The task is to draw the major organic product of this reaction, ignoring any inorganic byproducts.

### Reactants

1. **Benzene (C₆H₆):** Represented by a hexagon with alternating double bonds, indicating its aromatic structure.
   
2. **Benzoyl Chloride (C₆H₅COCl):** Composed of a benzene ring attached to a carbonyl group (C=O), which is connected to a chlorine atom (Cl).

### Reaction Conditions

- **Catalyst:** Aluminum chloride (AlCl₃) is used to facilitate the reaction.

### Reaction Type

This is a Friedel-Crafts acylation reaction, where an acyl group is introduced to the benzene ring.

### Expected Product

The Friedel-Crafts acylation will result in the attachment of the benzoyl group (C₆H₅CO-) to the benzene ring, forming benzophenone (C₆H₅COC₆H₅) as the major product.

### Mechanism Summary

1. **Formation of Acyl Cation:** AlCl₃ reacts with the chlorine atom in benzoyl chloride, helping to generate the acyl cation (C₆H₅C⁺=O).
   
2. **Electrophilic Aromatic Substitution:** The acyl cation acts as an electrophile and reacts with the benzene ring to form the acylated product.

This reaction exemplifies a key transformation in organic chemistry, used widely in the synthesis of aromatic ketones.
Transcribed Image Text:### Reaction Overview The image depicts a chemical reaction where benzene reacts with benzoyl chloride in the presence of aluminum chloride (AlCl₃) as a catalyst. The task is to draw the major organic product of this reaction, ignoring any inorganic byproducts. ### Reactants 1. **Benzene (C₆H₆):** Represented by a hexagon with alternating double bonds, indicating its aromatic structure. 2. **Benzoyl Chloride (C₆H₅COCl):** Composed of a benzene ring attached to a carbonyl group (C=O), which is connected to a chlorine atom (Cl). ### Reaction Conditions - **Catalyst:** Aluminum chloride (AlCl₃) is used to facilitate the reaction. ### Reaction Type This is a Friedel-Crafts acylation reaction, where an acyl group is introduced to the benzene ring. ### Expected Product The Friedel-Crafts acylation will result in the attachment of the benzoyl group (C₆H₅CO-) to the benzene ring, forming benzophenone (C₆H₅COC₆H₅) as the major product. ### Mechanism Summary 1. **Formation of Acyl Cation:** AlCl₃ reacts with the chlorine atom in benzoyl chloride, helping to generate the acyl cation (C₆H₅C⁺=O). 2. **Electrophilic Aromatic Substitution:** The acyl cation acts as an electrophile and reacts with the benzene ring to form the acylated product. This reaction exemplifies a key transformation in organic chemistry, used widely in the synthesis of aromatic ketones.
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