Chapter 14: Q.21558-14-27P. (page 557)
How many lines are observed in the 13C NMR spectrum of each compound?
a.

b.

c.

d.

Short Answer
a. Two lines
b. Four lines
c. Three lines
d. Four lines
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Chapter 14: Q.21558-14-27P. (page 557)
How many lines are observed in the 13C NMR spectrum of each compound?
a.

b.

c.

d.

a. Two lines
b. Four lines
c. Three lines
d. Four lines
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Question: For each compound, first label each different type of proton and then rank the protons in order of increasing chemical shift.
a.

b.

c.

Propose a structure for a compound of molecular formula C3H8O with an IR absorption at 3600 to 3200 cm-1 and the following NMR spectrum:

The reaction of (CH3)3 CCHO with (C6H5)3 P=C(CH3)OCH3 , followed by treatment with aqueous acid, afford R . R has strong absorption in its IR spectrum at 1717 cm-1 and three singlets in its -NMR spectrum at 1.02 (9 H), 2.13 (3 H), and 2.33 (2 H) ppm. What is the structure of R? We will learn about this reaction in Chapter 21.
Question: Explain why the carbonyl carbon of an aldehyde or ketone absorbs farther downfield than the carbonyl carbon of an ester in a 13C NMR spectrum
Question. In the presence of a small amount of acid, a solution of acetaldehyde(CH3CHO) in methanol (CH3OH) was allowed to stand and a new compound L was formed. L has a molecular ion in its mass spectrum at 90 and IR absorptions at 2992 and 2941cm-1 . L shows three signals in its 13C-NMR at 19, 52, and 101 ppm. 1H-NMR spectrum of L is given below. What is the structure of L?

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