Chapter 12: Q62E (page 354)
How would you prepare the following substances from 2-cyclohexenone? More than one step may be needed.
a.

b.

c.

d.

Short Answer
a.

b.

c.

d.

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Chapter 12: Q62E (page 354)
How would you prepare the following substances from 2-cyclohexenone? More than one step may be needed.
a.

b.

c.

d.

a.

b.

c.

d.

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Nitriles, R - C = N , undergo a hydrolysis reaction when heated with
aqueous acid. What is the structure of the compound produced by hydrolysis of propanenitrile, CH3CH2C=N , if it has IR absorptions from 2500-3100cm-1 and at 1710cm-1 , and has M+ = 74?
Question: The infrared spectrum of the compound with the mass spectrum shown below has a medium-intensity peak at about . There is also aC-H out-of-plane bending peak near . Propose a structure consistent with the data.

Question: What functional groups might the following molecules contain?
(a) A compound with a strong absorption at 1710
(b) A compound with a strong absorption at 1540
(c) A compound with strong absorptions at 1720 and 2500 to 3100
Question: Two infrared spectra are shown. One is the spectrum of cyclohexane,
and the other is the spectrum of cyclohexene. Identify them, and
explain your answer.
(a)

(b)

Propose structures for simple molecules that contain the following functional groups:
(a)Alcohol (b)Aromatic ring (c)Carboxylic acid (d)Amine (e)Both ketone and amine
(f) Two double bonds
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