CH,CH,OH major and minor products Br 1) 2) 3) 7)

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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### Organic Chemistry Reaction Mechanisms

**Reactant and Reaction Conditions:**

- **Reactant:** The molecule depicted in the top image is a substituted cyclohexane with a methyl group (CH₃) and two other substituents. One substituent is a bromine atom (Br) attached to one carbon, and an ethyl group attached to a different carbon.
- **Reaction Condition:** The reactant is subject to a reaction with ethanol (CH₃CH₂OH) as the reagent.

**Goal:** Identify the major and minor products of the reaction between the provided reactant and ethanol.

**Possible Reaction Products:**

1. **Product 1:** A substituted cyclohexane with an ethoxy group (OCH₂CH₃) at the former bromine position, with particular stereochemistry.
2. **Product 2:** A substituted cyclohexane with an ethoxy group (OCH₂CH₃) at the former bromine position, with a different stereochemistry than Product 1.
3. **Product 3:** Another configuration of the ethoxy group (OCH₂CH₃) attached at the former bromine position, highlighting a potential stereochemistry variant.
4. **Product 4:** The ethoxy group (OCH₂CH₃) attached similarly to Product 3 but differing in stereochemistry.
5. **Product 5:** A cyclohexene variant where the bromine has been removed, resulting in the formation of a double bond and a simpler methyl group present.
6. **Product 6:** Another cyclohexene derivative reflecting a different position of the double bond, maintaining a methyl group on the cyclohexane ring.
7. **Product 7:** Another structure resembling the cyclohexene pattern different from both products 5 and 6 in terms of double bond position.

### Explanation of the Diagram:

- The diagram showcases a specific type of organic reaction involving the substitution of a bromine atom by an ethoxy group from ethanol.
- Different stereochemical outcomes (3D orientations of atoms) are considered in the possible products.

### Concepts Applied:

- **Nucleophilic Substitution (SN1 and SN2)**
- **Elimination Reactions (E1 and E2)**
- **Stereochemistry:** Understanding of how atoms are spatially arranged in molecules, an essential part of organic chemistry to determine potential major and minor products.

### Key Take
Transcribed Image Text:### Organic Chemistry Reaction Mechanisms **Reactant and Reaction Conditions:** - **Reactant:** The molecule depicted in the top image is a substituted cyclohexane with a methyl group (CH₃) and two other substituents. One substituent is a bromine atom (Br) attached to one carbon, and an ethyl group attached to a different carbon. - **Reaction Condition:** The reactant is subject to a reaction with ethanol (CH₃CH₂OH) as the reagent. **Goal:** Identify the major and minor products of the reaction between the provided reactant and ethanol. **Possible Reaction Products:** 1. **Product 1:** A substituted cyclohexane with an ethoxy group (OCH₂CH₃) at the former bromine position, with particular stereochemistry. 2. **Product 2:** A substituted cyclohexane with an ethoxy group (OCH₂CH₃) at the former bromine position, with a different stereochemistry than Product 1. 3. **Product 3:** Another configuration of the ethoxy group (OCH₂CH₃) attached at the former bromine position, highlighting a potential stereochemistry variant. 4. **Product 4:** The ethoxy group (OCH₂CH₃) attached similarly to Product 3 but differing in stereochemistry. 5. **Product 5:** A cyclohexene variant where the bromine has been removed, resulting in the formation of a double bond and a simpler methyl group present. 6. **Product 6:** Another cyclohexene derivative reflecting a different position of the double bond, maintaining a methyl group on the cyclohexane ring. 7. **Product 7:** Another structure resembling the cyclohexene pattern different from both products 5 and 6 in terms of double bond position. ### Explanation of the Diagram: - The diagram showcases a specific type of organic reaction involving the substitution of a bromine atom by an ethoxy group from ethanol. - Different stereochemical outcomes (3D orientations of atoms) are considered in the possible products. ### Concepts Applied: - **Nucleophilic Substitution (SN1 and SN2)** - **Elimination Reactions (E1 and E2)** - **Stereochemistry:** Understanding of how atoms are spatially arranged in molecules, an essential part of organic chemistry to determine potential major and minor products. ### Key Take
For the given reaction, predict the major and minor products or not produced if the product is highly unlikely to form.
Transcribed Image Text:For the given reaction, predict the major and minor products or not produced if the product is highly unlikely to form.
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