Identify the compounds (draw the structures) that gives rise to the IR, mass, 'H NMR and 13C NMR spectra shown below. Be sure to show your thought processes to assure full credit. A. This compound has the formula C,HBrO2. Determine the structure of this compound. EDraw the structures of the fragments observed in the mass spectrum at 121/123 and 149/151. The BC NMR spectrum shows peaks at 14, 31, 56, 62, and 172 ppm 100 41 80 60 28 115 69 40 121 87 | 123 20 M(194) M+2(196) 149 151 40 80 120 160 200 m/z NEAT MICRONS 2.5 25 2.7 2.8 29 3 35 NICOLET 20SX FTIR 100 5.5 10 11 12 13 14 15 16 17 18 19 21 22 90 70 -R 0.1 30 A- 02 50 A. N. -A. 2.4 20 3.5 10 37 1738 cm -03 4000 1800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 20 450 WAVENUMBERS 800 600 Relative Abundance triplet quartet 10 8. 5 3 2.

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter12: Structure Determination: Mass Spectrometry And Infrared Spectroscopy
Section12.SE: Something Extra
Problem 48AP: The infrared spectrum of the compound with the mass spectrum shown below lacks any significant...
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This is a part of a practice worksheet that asks me to use H-NMR, C-NMR, Mass Spectroscopy, and IR Spectrum to answer the questions being asked. It will not be collected, but I want to make sure I understand it for our quiz next week. Thank you so much. :)

 

Identify the compounds (draw the structures) that gives rise to the IR, mass, 'H NMR and 13C NMR
spectra shown below. Be sure to show your thought processes to assure full credit.
A.
This compound has the formula C,HBrO2. Determine the structure of this compound. EDraw the
structures of the fragments observed in the mass spectrum at 121/123 and 149/151. The BC NMR
spectrum shows peaks at 14, 31, 56, 62, and 172 ppm
100
41
80
60
28
115
69
40
121
87
| 123
20
M(194)
M+2(196)
149 151
40
80
120
160
200
m/z
NEAT
MICRONS
2.5 25 2.7 2.8 29 3
35
NICOLET 20SX FTIR
100
5.5
10
11
12
13
14
15 16 17 18 19
21 22
90
70
-R
0.1
30
A-
02
50
A.
N.
-A.
2.4
20
3.5
10
37
1738 cm
-03
4000
1800
3600
3400 3200 3000
2800 2600 2400 2200
2000
1800
1600
1400
1200
1000
20
450
WAVENUMBERS
800
600
Relative Abundance
Transcribed Image Text:Identify the compounds (draw the structures) that gives rise to the IR, mass, 'H NMR and 13C NMR spectra shown below. Be sure to show your thought processes to assure full credit. A. This compound has the formula C,HBrO2. Determine the structure of this compound. EDraw the structures of the fragments observed in the mass spectrum at 121/123 and 149/151. The BC NMR spectrum shows peaks at 14, 31, 56, 62, and 172 ppm 100 41 80 60 28 115 69 40 121 87 | 123 20 M(194) M+2(196) 149 151 40 80 120 160 200 m/z NEAT MICRONS 2.5 25 2.7 2.8 29 3 35 NICOLET 20SX FTIR 100 5.5 10 11 12 13 14 15 16 17 18 19 21 22 90 70 -R 0.1 30 A- 02 50 A. N. -A. 2.4 20 3.5 10 37 1738 cm -03 4000 1800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 20 450 WAVENUMBERS 800 600 Relative Abundance
triplet
quartet
10
8.
5
3
2.
Transcribed Image Text:triplet quartet 10 8. 5 3 2.
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