Chapter 17: Q.12. (page 641)
Question: Which heterocycles are aromatic?
a.

b.

c.

d.

Short Answer
Answer
- Aromatic
- Aromatic
- Non-aromatic
- Aromatic
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Chapter 17: Q.12. (page 641)
Question: Which heterocycles are aromatic?
a.

b.

c.

d.

Answer
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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: Januvia, the trade name for sitagliptin, was introduced in 2006 for the treatment of type 2 diabetes. (a) Explain why the five-membered ring in sitagliptin is aromatic. (b) Determine the hybridization of each N atom. (c) In what type of orbital does the lone pair on each N atom reside?

Question: The purine heterocycle occurs commonly in the structure of DNA.

a. How is each N atom hybridized?
b. In what type of orbital does each lone pair on a N atom reside?
c. How many electrons does purine contain?
d. Why is purine aromatic?
Question: Classify each compound as aromatic, antiaromatic, or not aromatic.
Question: Which of the diethylbenzene isomers (ortho, meta, or para) corresponds to each set of NMR spectral data?
[A] NMR signals: 16, 29, 125, 127.5, 128.4, and 144 ppm
[B] NMR signals: 15, 26, 126, 128, and 142 ppm
[C] NMR signals: 16, 29, 128, and 141 ppm
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