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

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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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