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6. How would you convert the following compounds to aromatic compounds? -OH a. b. 7. In each case below, explain the enhanced reactivity. OH cyclohexyl bromide OH dehydrates more readily than a. b. 8. Benzylic intermediates are more stable than simple alkyl intermediates. a. Use resonance forms to show the delocalization electrons of the electrons for the structures below. Br Benzylic position b. Which of the following reactions will be faster? Explain, and be sure to provide the transition state of the reaction to explain your answer. Br NaOCH 3 benzyl bromide is more basic than NaOCH3 d. OMe OMe

6. How would you convert the following compounds to aromatic compounds? -OH a. b. 7. In each case below, explain the enhanced reactivity. OH cyclohexyl bromide OH dehydrates more readily than a. b. 8. Benzylic intermediates are more stable than simple alkyl intermediates. a. Use resonance forms to show the delocalization electrons of the electrons for the structures below. Br Benzylic position b. Which of the following reactions will be faster? Explain, and be sure to provide the transition state of the reaction to explain your answer. Br NaOCH 3 benzyl bromide is more basic than NaOCH3 d. OMe OMe

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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#6 and 8 please 
6. How would you convert the following compounds to aromatic compounds? -OH a. b. 7. In each case below, explain the enhanced reactivity. OH cyclohexyl bromide OH dehydrates more readily than a. b. 8. Benzylic intermediates are more stable than simple alkyl intermediates. a. Use resonance forms to show the delocalization electrons of the electrons for the structures below. Br Benzylic position b. Which of the following reactions will be faster? Explain, and be sure to provide the transition state of the reaction to explain your answer. Br NaOCH3 benzyl bromide is more basic than NaOCH3 d. OMe OMe
Transcribed Image Text:6. How would you convert the following compounds to aromatic compounds? -OH a. b. 7. In each case below, explain the enhanced reactivity. OH cyclohexyl bromide OH dehydrates more readily than a. b. 8. Benzylic intermediates are more stable than simple alkyl intermediates. a. Use resonance forms to show the delocalization electrons of the electrons for the structures below. Br Benzylic position b. Which of the following reactions will be faster? Explain, and be sure to provide the transition state of the reaction to explain your answer. Br NaOCH3 benzyl bromide is more basic than NaOCH3 d. OMe OMe
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