Chapter 17: Problem 17.1 (page 644)
Draw all possible resonance structures for the antihistamine diphenhydramine, the active ingredient in Benadryl.
Short Answer
Answer
Resonating structures of diphenhydramine.
Chapter 17: Problem 17.1 (page 644)
Draw all possible resonance structures for the antihistamine diphenhydramine, the active ingredient in Benadryl.
Answer
Resonating structures of diphenhydramine.
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Get started for freeQuestion: Compounds A and B are both hydrogenated to methylcyclohexane. Which compound has the larger heat of hydrogenation? Which compound is more stable?
Question:
a. Draw all reasonable resonance structures for pyrrole and explain why pyrrole is less resonance stabilized than benzene.
b. Draw all reasonable resonance structures for furan and explain why furan is less resonance stabilized than pyrrole.
Question: Draw the conjugate bases of pyrrole and cyclopentadiene. Explain why the hybridized C-H bond of cyclopentadiene is more acidic than the N-H bond of pyrrole.
Question: Draw additional resonance structures for each species.
Question: Use the inscribed polygon method to show why the following cation is aromatic.
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