10. The methoxy group in anisole, below at left, is a donating group. Draw its resonance structures (fill in à bonds and charges) to show which ring carbons are made more nucleophilic (that is, electron-rich) by the donating group. H3C-Ö: H3C H3C H3C- 11. Draw the first nitration product when acetophenone (above) is treated with nitric acid and sulfuric acid. Then, do the same with anisole (also above). Which reaction is faster?
10. The methoxy group in anisole, below at left, is a donating group. Draw its resonance structures (fill in à bonds and charges) to show which ring carbons are made more nucleophilic (that is, electron-rich) by the donating group. H3C-Ö: H3C H3C H3C- 11. Draw the first nitration product when acetophenone (above) is treated with nitric acid and sulfuric acid. Then, do the same with anisole (also above). Which reaction is faster?
Chemistry
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Chapter1: Chemical Foundations
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![10. The methoxy group in anisole, below at left, is a donating group. Draw its resonance
structures (fill in à bonds and charges) to show which ring carbons are made more nucleophilic
(that is, electron-rich) by the donating group.
H3C-Ö:
H3C
H3C
H3C-
11. Draw the first nitration product when acetophenone (above) is treated with nitric acid and
sulfuric acid. Then, do the same with anisole (also above). Which reaction is faster?](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F11d828c5-2fca-41e0-a2f6-f66d4f987aa1%2F300b98d6-ad04-49ef-9a68-4936be55cfd9%2Fs6kdcg_processed.png&w=3840&q=75)
Transcribed Image Text:10. The methoxy group in anisole, below at left, is a donating group. Draw its resonance
structures (fill in à bonds and charges) to show which ring carbons are made more nucleophilic
(that is, electron-rich) by the donating group.
H3C-Ö:
H3C
H3C
H3C-
11. Draw the first nitration product when acetophenone (above) is treated with nitric acid and
sulfuric acid. Then, do the same with anisole (also above). Which reaction is faster?
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