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 ЗА: С H12O2 100 60- ស 4.5 4000 2Н 68:4062 €8 8962 3.0 2500 5 сл 2000 2Н 1738.08 1464.16 1500 1371.53 2H 1255.82 1.5 1186.37 1095.71 1028.19 bum . ЗН зн 1.0 PPM 0.5

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
ChapterL4: Proton (1h) Nmr Spectroscopy
Section: Chapter Questions
Problem 3E: Here are proton NMR data for 1-bromopropane: Ha : triplet (2H) 3.32ppm; Hb : multiplet (2H)1.81ppm;...
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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
ЗА: С H12O2
100
60-
ស
4.5
4000
2Н
68:4062 €8 8962
3.0
2500
5
сл
2000
2Н
1738.08
1464.16
1500
1371.53
2H
1255.82
1.5
1186.37
1095.71
1028.19
bum
.
ЗН
зн
1.0 PPM
0.5
Transcribed Image Text:ЗА: С H12O2 100 60- ស 4.5 4000 2Н 68:4062 €8 8962 3.0 2500 5 сл 2000 2Н 1738.08 1464.16 1500 1371.53 2H 1255.82 1.5 1186.37 1095.71 1028.19 bum . ЗН зн 1.0 PPM 0.5
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