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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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1. Choose the correct chair conformation of the cyclohexane that can undergo E2 elimination [Select] 2. Choose the correct transition state for E2 elimination using NaOtBu as the base (Select] 3. Choose the correct elimination product [Select] 4. State whether a solution of the product would be optically active or not [Select] D Br 1. E2 Chair 1-Bu t-Bu t-But A 2. E2 Transition State Et A O-1-Bu Br Br # O NaOtBu l-Bu t-Bu -Bu B B Et B V Br Br 0-1-But V 1-Bu Ⓒ L-Bu C Br H El: с 3. E2 Product Et Et & ggg t-Bu 1-Bu A C O-t-Bu Br D 1-Bu Ⓒ 1-Bu 5 D Br H O-1-Bu + O
Transcribed Image Text:1. Choose the correct chair conformation of the cyclohexane that can undergo E2 elimination [Select] 2. Choose the correct transition state for E2 elimination using NaOtBu as the base (Select] 3. Choose the correct elimination product [Select] 4. State whether a solution of the product would be optically active or not [Select] D Br 1. E2 Chair 1-Bu t-Bu t-But A 2. E2 Transition State Et A O-1-Bu Br Br # O NaOtBu l-Bu t-Bu -Bu B B Et B V Br Br 0-1-But V 1-Bu Ⓒ L-Bu C Br H El: с 3. E2 Product Et Et & ggg t-Bu 1-Bu A C O-t-Bu Br D 1-Bu Ⓒ 1-Bu 5 D Br H O-1-Bu + O
1. Choose the correct chair conformation of the cyclohexane that can undergo E2 elimination (Select] 2. Choose the correct transition state for E2 elimination using NaOtBu as the base [Select] 3. Choose the correct elimination product [Select] [Select] A 4. State whether a solution of the product B active or not [Select] C D Br 1. E2 Chair t-Bu 1-Bu t-Bu A 2. E2 Transition State H A 3. E2 Product Et t-Bu A O-1-Bu .Br Et Br + O NaOtBu l-Bu t-Bu T 1-Bu B B Et Br 0-1-Bu t $][ Br B V 1-Bu C Et 1-Bu CAS C Br L-Bu D H--O-t-Bu C Br -Bu D Et O 1-Bu D Et 1-Bu H Br D O-L-Bu Br
Transcribed Image Text:1. Choose the correct chair conformation of the cyclohexane that can undergo E2 elimination (Select] 2. Choose the correct transition state for E2 elimination using NaOtBu as the base [Select] 3. Choose the correct elimination product [Select] [Select] A 4. State whether a solution of the product B active or not [Select] C D Br 1. E2 Chair t-Bu 1-Bu t-Bu A 2. E2 Transition State H A 3. E2 Product Et t-Bu A O-1-Bu .Br Et Br + O NaOtBu l-Bu t-Bu T 1-Bu B B Et Br 0-1-Bu t $][ Br B V 1-Bu C Et 1-Bu CAS C Br L-Bu D H--O-t-Bu C Br -Bu D Et O 1-Bu D Et 1-Bu H Br D O-L-Bu Br
Expert Solution
Step 1: Bimolecular elimination reaction

Bimolecular elimination reaction the rate of reaction depends upon concentration of both reactant and base.

It is single step reaction and preferred anti-elimination. 

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