Predict the Major product(s) for the following reactions. (10 pts total) Ph Ph mechanism: Show the correct stereochemistry when needed!! mechanism: CI Ph Br H₂S substitution. CH₂ONa DMF A elimination
Predict the Major product(s) for the following reactions. (10 pts total) Ph Ph mechanism: Show the correct stereochemistry when needed!! mechanism: CI Ph Br H₂S substitution. CH₂ONa DMF A elimination
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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![**Predict the Major product(s) for the following reactions. (10 pts total)**
**Show the correct stereochemistry when needed!!**
---
**First Reaction:**
- Structure:
- Starting compound: A cyclohexane ring with two phenyl (Ph) groups and a chlorine (Cl) atom attached.
- Reactant: \[\text{H}_2\text{S}\]
- Reaction type: Substitution
- **Mechanism:**
- The reaction involves the substitution of the chlorine atom by hydrogen sulfide, based on a nucleophilic substitution mechanism.
- **Product Box:**
- There is a blank box where the major product should be drawn, showing the substitution product.
---
**Second Reaction:**
- Structure:
- Starting compound: A cyclohexane ring with a phenyl (Ph) group and a bromine (Br) atom attached.
- Reactant: \[\text{CH}_3\text{ONa}\]
- Solvent: DMF
- Heat: Indicated by the delta (\[\Delta\]) symbol.
- Reaction type: Elimination
- **Mechanism:**
- This reaction involves elimination, where \[\text{CH}_3\text{ONa}\] acts as a base to eliminate the bromine atom, forming a double bond. The involvement of the solvent DMF and heat suggests an E2 mechanism.
- **Product Box:**
- There is a blank box where the major product should be drawn, showing the elimination product with correct stereochemistry.
---
**Note:** Ensure to draw the correct stereochemical configuration for each product as part of the mechanism illustration.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F9ce06757-d6de-4267-b0ea-44fd39b8f6a4%2F7c642fbb-64e6-4e8d-86d6-d1c859ea57d8%2Fs9ylrlx_processed.png&w=3840&q=75)
Transcribed Image Text:**Predict the Major product(s) for the following reactions. (10 pts total)**
**Show the correct stereochemistry when needed!!**
---
**First Reaction:**
- Structure:
- Starting compound: A cyclohexane ring with two phenyl (Ph) groups and a chlorine (Cl) atom attached.
- Reactant: \[\text{H}_2\text{S}\]
- Reaction type: Substitution
- **Mechanism:**
- The reaction involves the substitution of the chlorine atom by hydrogen sulfide, based on a nucleophilic substitution mechanism.
- **Product Box:**
- There is a blank box where the major product should be drawn, showing the substitution product.
---
**Second Reaction:**
- Structure:
- Starting compound: A cyclohexane ring with a phenyl (Ph) group and a bromine (Br) atom attached.
- Reactant: \[\text{CH}_3\text{ONa}\]
- Solvent: DMF
- Heat: Indicated by the delta (\[\Delta\]) symbol.
- Reaction type: Elimination
- **Mechanism:**
- This reaction involves elimination, where \[\text{CH}_3\text{ONa}\] acts as a base to eliminate the bromine atom, forming a double bond. The involvement of the solvent DMF and heat suggests an E2 mechanism.
- **Product Box:**
- There is a blank box where the major product should be drawn, showing the elimination product with correct stereochemistry.
---
**Note:** Ensure to draw the correct stereochemical configuration for each product as part of the mechanism illustration.
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