Based on the spectra provided, draw the structure. Label each unique carbon and hydrogen with the letters A, B, C… for use in assigning NMR peaks. fill in the data table assigning peaks in each spectrum. You should assign: • All 1H NMR peaks • Significant IR peaks above 1600 cm Example of what the table should include (imagine the structure of ethanol is drawn with the CH3 hydrogens labeled as A, the CH2 hydrogens labeled as B, and the OH hydrogen labeled as C) : hydrogen proton chemical shift integration splitting pattern couples to.. A 1.2 3 triplet B B 3.7 2 quartet A C 2.6 1 singlet -
Based on the spectra provided, draw the structure. Label each unique carbon and hydrogen with the letters A, B, C… for use in assigning NMR peaks. fill in the data table assigning peaks in each spectrum. You should assign: • All 1H NMR peaks • Significant IR peaks above 1600 cm Example of what the table should include (imagine the structure of ethanol is drawn with the CH3 hydrogens labeled as A, the CH2 hydrogens labeled as B, and the OH hydrogen labeled as C) : hydrogen proton chemical shift integration splitting pattern couples to.. A 1.2 3 triplet B B 3.7 2 quartet A C 2.6 1 singlet -
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Question
Based on the spectra provided, draw the structure. Label each unique carbon and hydrogen with the letters A, B, C… for use in assigning NMR peaks. fill in the data table assigning peaks in each spectrum. You should assign:
• All 1H NMR peaks
• Significant IR peaks above 1600 cm
Example of what the table should include (imagine the structure of ethanol is drawn with the CH3 hydrogens labeled as A, the CH2 hydrogens labeled as B, and the OH hydrogen labeled as C) :
hydrogen | proton chemical shift | integration | splitting pattern | couples to.. |
A | 1.2 | 3 | triplet | B |
B | 3.7 | 2 | quartet | A |
C | 2.6 | 1 | singlet | - |
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240
12
220
11
200
10
QE-300
180
9
160
8
140
7
120
6
100
5
80
4
60
3
40
2
20
1
0
0"
Transcribed Image Text:CDC13
240
12
220
11
200
10
QE-300
180
9
160
8
140
7
120
6
100
5
80
4
60
3
40
2
20
1
0
0
![The M+ peak is at 206 m/z.
Relative Intensity
100
80
60
40
20
0
L
CC
20
100
%T
80
60
40
20
4000
40
60
3000
80
100
2000
120
Wave number (cm-¹) and Transmittance (T%)
3065 73 1605 75 1295 34
1097 45 820 82
3029 63 1498 53
1253 44
1053 68 749 50
1186 27
1031 65
699 34
2960 30 1455 45
2872 55 1388 56
1737 12 1369 55
1168 30
1002 47
570 77
1120 41
908 82 496 68
m/z
1500
Wavenumber [cm-¹]
140 160 180 200 220 240
W
1000
400](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ff57d3743-5e44-4060-83da-5d90a37d31c6%2Fc74419e8-639d-4085-9e95-9906a96b100d%2F4zq26y_processed.png&w=3840&q=75)
Transcribed Image Text:The M+ peak is at 206 m/z.
Relative Intensity
100
80
60
40
20
0
L
CC
20
100
%T
80
60
40
20
4000
40
60
3000
80
100
2000
120
Wave number (cm-¹) and Transmittance (T%)
3065 73 1605 75 1295 34
1097 45 820 82
3029 63 1498 53
1253 44
1053 68 749 50
1186 27
1031 65
699 34
2960 30 1455 45
2872 55 1388 56
1737 12 1369 55
1168 30
1002 47
570 77
1120 41
908 82 496 68
m/z
1500
Wavenumber [cm-¹]
140 160 180 200 220 240
W
1000
400
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