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Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Please Draw the major product for the reaction 

This image depicts a chemical reaction known as Friedel-Crafts alkylation. It involves the following components:

- **Reactants:**
  - A benzene ring, symbolized by a hexagon with alternating double bonds.
  - A cyclohexyl chloride compound, represented as a cyclohexane ring (hexagon) with a single chlorine (Cl) atom attached.

- **Catalyst:**
  - Aluminum chloride (AlCl₃), which is specified below the reaction arrow.

- **Reaction Arrow:**
  - An arrow pointing right, indicating the direction of the reaction, implying the formation of a product when benzene and cyclohexyl chloride react in the presence of AlCl₃.

This setup describes a common organic chemistry reaction used to introduce alkyl groups into aromatic rings. The aluminum chloride serves as a catalyst, facilitating the reaction by forming a complex with the chloride, making the alkyl group more electrophilic and enabling it to attach to the benzene ring. The resulting product is a substituted aromatic compound.
Transcribed Image Text:This image depicts a chemical reaction known as Friedel-Crafts alkylation. It involves the following components: - **Reactants:** - A benzene ring, symbolized by a hexagon with alternating double bonds. - A cyclohexyl chloride compound, represented as a cyclohexane ring (hexagon) with a single chlorine (Cl) atom attached. - **Catalyst:** - Aluminum chloride (AlCl₃), which is specified below the reaction arrow. - **Reaction Arrow:** - An arrow pointing right, indicating the direction of the reaction, implying the formation of a product when benzene and cyclohexyl chloride react in the presence of AlCl₃. This setup describes a common organic chemistry reaction used to introduce alkyl groups into aromatic rings. The aluminum chloride serves as a catalyst, facilitating the reaction by forming a complex with the chloride, making the alkyl group more electrophilic and enabling it to attach to the benzene ring. The resulting product is a substituted aromatic compound.
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