2A: C5H₁2O 100- 80 60 40- 20 0 TTTTT 4000 3.0 2.8 3500 2.6 3377 2.4 2928 -2970 3000 1H 2.2 2.0 2500 1.8 1.6 2000 2H ли 1.4 6H 1.2 1464 1500 1375 1.0 1277 3H 9811 0.8 1060 939 1000 188 וד 0.6 PPM 0.4 For each problem, you must: 1) Calculate the degree of unsaturation. -1 2) Assign the principal IR absorption bands above 1500 cm 3) Draw the structure of the compound 4) Label the protons on your structure with letters and assign them to peaks on the NMR spectrum (see the example below). 4.0 C 2H 3.5 3.0 2.5 D 1H 3.0 This peak is a magnified version of this peak A 2.8 2.0 1H B zum 2.6 B 2H Each problem contains the formula of the compound, the IR spectrum (with axes in cm³¹ vs. % transmission), and the ¹H NMR spectrum (with axis in PPM shift). Some NMR spectra show a peak hovering above the baseline. This is a magnified view of one of the actual peaks, to allow you to see splitting more clearly. 1.5 2.4 OHD A 3H 1.0 PPM 0.5

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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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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2A: C5H₁2O
100-
80
60
40-
20
0
TTTTT
4000
3.0
2.8
3500
2.6
3377
2.4
2928
-2970
3000
1H
2.2
2.0
2500
1.8
1.6
2000
2H
ли
1.4
6H
1.2
1464
1500
1375
1.0
1277
3H
9811
0.8
1060
939
1000
188
וד
0.6 PPM 0.4
Transcribed Image Text:2A: C5H₁2O 100- 80 60 40- 20 0 TTTTT 4000 3.0 2.8 3500 2.6 3377 2.4 2928 -2970 3000 1H 2.2 2.0 2500 1.8 1.6 2000 2H ли 1.4 6H 1.2 1464 1500 1375 1.0 1277 3H 9811 0.8 1060 939 1000 188 וד 0.6 PPM 0.4
For each problem, you must:
1) Calculate the degree of unsaturation.
-1
2) Assign the principal IR absorption bands above 1500 cm
3) Draw the structure of the compound
4) Label the protons on your structure with letters and assign them to peaks on the NMR spectrum
(see the example below).
4.0
C
2H
3.5
3.0
2.5
D
1H
3.0
This peak
is a magnified
version of
this peak
A
2.8
2.0
1H
B
zum
2.6
B
2H
Each problem contains the formula of the compound, the IR spectrum (with axes in cm³¹ vs. %
transmission), and the ¹H NMR spectrum (with axis in PPM shift). Some NMR spectra show a peak
hovering above the baseline. This is a magnified view of one of the actual peaks, to allow you to see
splitting more clearly.
1.5
2.4
OHD
A
3H
1.0 PPM
0.5
Transcribed Image Text:For each problem, you must: 1) Calculate the degree of unsaturation. -1 2) Assign the principal IR absorption bands above 1500 cm 3) Draw the structure of the compound 4) Label the protons on your structure with letters and assign them to peaks on the NMR spectrum (see the example below). 4.0 C 2H 3.5 3.0 2.5 D 1H 3.0 This peak is a magnified version of this peak A 2.8 2.0 1H B zum 2.6 B 2H Each problem contains the formula of the compound, the IR spectrum (with axes in cm³¹ vs. % transmission), and the ¹H NMR spectrum (with axis in PPM shift). Some NMR spectra show a peak hovering above the baseline. This is a magnified view of one of the actual peaks, to allow you to see splitting more clearly. 1.5 2.4 OHD A 3H 1.0 PPM 0.5
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