Problems 285 23. The NMR spectra are shown in parts a, b, c, and d for four isomeric compounds with formula CioH12O2. Their infrared spectra show strong bands near 1735 cm, Make no attempt to inter- pret the aromatic proton area between 7.0 and 7.5 ppm except to determine the number of pro- tons attached to the aromatic ring. Draw the structures of the compounds. CioH1202 4.84 7.5 7.0 2.06 2.05 3.01 55 5.0 4.5 4.0 3.5 30 25 20 LS (a) Ci0H1202 317 4.94 70 2.08 2.04 3.13 23 3.0 35

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Nuclear Magnetic Resonance Spectroscopy • Part Ole
286
C1OH12O2
4.85
7.5
7.0
2.05
2,93
2.04
3.0
2.5
2.0
4.0
(c)
C10H1202
4.86
0.97
7.0
6.0
3.02
2.98
5.0
4.0
2.5
2.0
1.5
(d)
Transcribed Image Text:Nuclear Magnetic Resonance Spectroscopy • Part Ole 286 C1OH12O2 4.85 7.5 7.0 2.05 2,93 2.04 3.0 2.5 2.0 4.0 (c) C10H1202 4.86 0.97 7.0 6.0 3.02 2.98 5.0 4.0 2.5 2.0 1.5 (d)
Problems
285
23. The NMR spectra are shown in parts a, b, c, and d for four isomeric compounds with formula
CH1202. Their infrared spectra show strong bands near 1735 cm', Make no attempt to inter-
pret the aromatic proton area between 7.0 and 7.5 ppm except to determine the number of pro-
tons attached to the aromatic ring. Draw the structures of the compounds.
C10H1202
4.84
7.0
2.06
2.05
3.01
(a)
C10H1202
in
3M
4.94
7.0
2.08
2.04
3.13
3.0
(b)
Transcribed Image Text:Problems 285 23. The NMR spectra are shown in parts a, b, c, and d for four isomeric compounds with formula CH1202. Their infrared spectra show strong bands near 1735 cm', Make no attempt to inter- pret the aromatic proton area between 7.0 and 7.5 ppm except to determine the number of pro- tons attached to the aromatic ring. Draw the structures of the compounds. C10H1202 4.84 7.0 2.06 2.05 3.01 (a) C10H1202 in 3M 4.94 7.0 2.08 2.04 3.13 3.0 (b)
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