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10. When cyclohexane 5 is treated with a strong base it undergoes an E2 elimination. Answer the following questions about the reaction below. a) Draw the structure of the favored product for the E2 reaction 5 'Br Na b) Draw the two chair conformations for cylcohexane 5. (Make sure to draw out all groups including hydrogens.) c) Put a square around the most stable chair and circle the reactive conformation. d) The elimination of 5 proceeds much faster than the elimination of 6, which produces a different alkene product 7. Explain the difference in rate and the formation of a different alkene product. Explanation NaOCH3 slow Br 7 6

10. When cyclohexane 5 is treated with a strong base it undergoes an E2 elimination. Answer the following questions about the reaction below. a) Draw the structure of the favored product for the E2 reaction 5 'Br Na b) Draw the two chair conformations for cylcohexane 5. (Make sure to draw out all groups including hydrogens.) c) Put a square around the most stable chair and circle the reactive conformation. d) The elimination of 5 proceeds much faster than the elimination of 6, which produces a different alkene product 7. Explain the difference in rate and the formation of a different alkene product. Explanation NaOCH3 slow Br 7 6

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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10. When cyclohexane 5 is treated with a strong base it undergoes an E2 elimination. Answer the following questions about the reaction below. a) Draw the structure of the favored product for the E2 reaction 5 'Br Na b) Draw the two chair conformations for cylcohexane 5. (Make sure to draw out all groups including hydrogens.) c) Put a square around the most stable chair and circle the reactive conformation. d) The elimination of 5 proceeds much faster than the elimination of 6, which produces a different alkene product 7. Explain the difference in rate and the formation of a different alkene product. Explanation NaOCH3 slow Br 7 6
Transcribed Image Text:10. When cyclohexane 5 is treated with a strong base it undergoes an E2 elimination. Answer the following questions about the reaction below. a) Draw the structure of the favored product for the E2 reaction 5 'Br Na b) Draw the two chair conformations for cylcohexane 5. (Make sure to draw out all groups including hydrogens.) c) Put a square around the most stable chair and circle the reactive conformation. d) The elimination of 5 proceeds much faster than the elimination of 6, which produces a different alkene product 7. Explain the difference in rate and the formation of a different alkene product. Explanation NaOCH3 slow Br 7 6
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