To preview image click here & For the following reactions assign the mechanism as E1, E2, SN1, SN2 1. Choose the correct option for A [Select] 2. Choose the correct option for B [Select] 3. Choose the correct option for C[Select] 4. Choose the correct option for D [Select] CI A. B. C. D. Br Br Br CH3OH heat NaOMe CH3SNa NaOEt
To preview image click here & For the following reactions assign the mechanism as E1, E2, SN1, SN2 1. Choose the correct option for A [Select] 2. Choose the correct option for B [Select] 3. Choose the correct option for C[Select] 4. Choose the correct option for D [Select] CI A. B. C. D. Br Br Br CH3OH heat NaOMe CH3SNa NaOEt
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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![For the following reactions, assign the mechanism as E1, E2, SN1, or SN2:
- **A:** A compound with two phenyl groups and a chlorine atom, reacts with CH₃OH and heat.
- **B:** A bromocyclohexane compound reacts with NaOMe.
- **C:** A 2-bromobutane compound reacts with CH₃SNa.
- **D:** A bromocyclopentane compound reacts with NaOEt.
Each reaction has a dropdown menu to select the mechanism type (E1, E2, SN1, SN2).
**Explanation of Diagrams:**
1. **Compound A:** Contains two aromatic rings with a chlorine atom attached. The reaction involves methanol and heat, suggesting a possible substitution or elimination mechanism.
2. **Compound B:** Cyclohexane ring with a bromine substituent. The reaction with sodium methoxide suggests a nucleophilic substitution or elimination.
3. **Compound C:** Linear carbon chain with a bromine substituent at the second carbon, reacting with sodium thiomethoxide, indicating substitution.
4. **Compound D:** Cyclopentane ring with a bromine substituent, reacting with sodium ethoxide, suggesting substitution or elimination pathways.
Each reaction type can be analyzed based on the structure of the reactants and the conditions provided.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F4570aa97-d31b-43f1-9c0f-902fd4186789%2Fb8b9060c-6b23-4830-91bb-8c0495f364a5%2F8ap73pi_processed.jpeg&w=3840&q=75)
Transcribed Image Text:For the following reactions, assign the mechanism as E1, E2, SN1, or SN2:
- **A:** A compound with two phenyl groups and a chlorine atom, reacts with CH₃OH and heat.
- **B:** A bromocyclohexane compound reacts with NaOMe.
- **C:** A 2-bromobutane compound reacts with CH₃SNa.
- **D:** A bromocyclopentane compound reacts with NaOEt.
Each reaction has a dropdown menu to select the mechanism type (E1, E2, SN1, SN2).
**Explanation of Diagrams:**
1. **Compound A:** Contains two aromatic rings with a chlorine atom attached. The reaction involves methanol and heat, suggesting a possible substitution or elimination mechanism.
2. **Compound B:** Cyclohexane ring with a bromine substituent. The reaction with sodium methoxide suggests a nucleophilic substitution or elimination.
3. **Compound C:** Linear carbon chain with a bromine substituent at the second carbon, reacting with sodium thiomethoxide, indicating substitution.
4. **Compound D:** Cyclopentane ring with a bromine substituent, reacting with sodium ethoxide, suggesting substitution or elimination pathways.
Each reaction type can be analyzed based on the structure of the reactants and the conditions provided.
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