Chapter 14: Q.21558-14-14P. (page 546)
Into how many peaks will each proton shown in green be split?
a.
b.
c.
d.
e.
f.
Short Answer
a. 3 and 4
b. 2 and 4
c. 1, 3, and 3
d. 2 and 2
e. 2 and 2
f. 2 and 3
Chapter 14: Q.21558-14-14P. (page 546)
Into how many peaks will each proton shown in green be split?
a.
b.
c.
d.
e.
f.
a. 3 and 4
b. 2 and 4
c. 1, 3, and 3
d. 2 and 2
e. 2 and 2
f. 2 and 3
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Get started for freeQuestion: As we will learn in Chapter 20, reaction of (CH3)2CO with followed by affords compound D, which has a molecular ion in its mass spectrum at 84 and prominent absorptions in its IR spectrum at 3600โ3200, 3303, 2938, and 2120cm-1 . D shows the following 1 H NMR spectral data: 1.53 (singlet, 6 H), 2.37 (singlet, 1 H), and 2.43 (singlet, 1 H) ppm. What is the structure of D?
Propose a structure consistent with each set of data.
a. Compound J: molecular ion at 72; IR peak at 1710cm-1 ; 1H -NMR data (ppm) at 1.0 (triplet, 3 H), 2.1 (singlet, 3 H), and 2.4 (quartet, 2 H)
b. Compound K: molecular ion at 88; IR peak at 3600โ3200 ;1H-NMR data (ppm) at 0.9 (triplet, 3 H), 1.2 (singlet, 6 H), 1.5 (quartet, 2 H), and 1.6 (singlet, 1 H)
Question: The 1 H NMR spectrum of N,N-dimethylformamide shows three singlets at 2.9, 3.0, and 8.0 ppm. Explain why the two groups are not equivalent to each other, thus giving rise to two NMR signals.
Question: Which of the labeled protons in each pair absorbs farther downfield?
Question: Into how many peaks will the signal for each of the labeled protons be split?
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