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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
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.
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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