Cl2 CH3CH2OH

Chemistry
10th Edition
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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Draw the product and it's enantiomer 

The image depicts a chemical reaction. 

### Chemical Reaction Details:

**Reactant:**
- The reactant is a cyclohexene molecule with an alkene side chain. The cyclohexane ring is attached to a propenyl group (CH₃CH=CH₂).

**Reaction Conditions:**
- The reaction involves chlorine (Cl₂) as a reagent.
- The solvent used in this reaction is ethanol (CH₃CH₂OH).

**Product:**
- The exact product is not shown, but typically, such a reaction would result in the addition of chlorine across the double bond of the alkene, forming a dichlorinated compound.

### Reaction Explanation:
In this electrophilic addition reaction, chlorine acts as an electrophile and adds to the double bond in the alkene side chain of the cyclohexene, potentially leading to vicinal dichlorination. The solvent, ethanol, provides an environment that may stabilize intermediate species or affect the reaction pathway, although it is not directly involved in the addition reaction.

This type of reaction is commonly used to demonstrate the concept of electrophilic addition in organic chemistry, showcasing how halogens can add to alkenes to form more saturated molecules.
Transcribed Image Text:The image depicts a chemical reaction. ### Chemical Reaction Details: **Reactant:** - The reactant is a cyclohexene molecule with an alkene side chain. The cyclohexane ring is attached to a propenyl group (CH₃CH=CH₂). **Reaction Conditions:** - The reaction involves chlorine (Cl₂) as a reagent. - The solvent used in this reaction is ethanol (CH₃CH₂OH). **Product:** - The exact product is not shown, but typically, such a reaction would result in the addition of chlorine across the double bond of the alkene, forming a dichlorinated compound. ### Reaction Explanation: In this electrophilic addition reaction, chlorine acts as an electrophile and adds to the double bond in the alkene side chain of the cyclohexene, potentially leading to vicinal dichlorination. The solvent, ethanol, provides an environment that may stabilize intermediate species or affect the reaction pathway, although it is not directly involved in the addition reaction. This type of reaction is commonly used to demonstrate the concept of electrophilic addition in organic chemistry, showcasing how halogens can add to alkenes to form more saturated molecules.
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