Complete the spectroscopy data tables for a compound with molecular formula C5H13N. Determine the structure of the compound. Any labile protons, if they exist, will not be present in this particular 1H NMR spectrum.
Complete the spectroscopy data tables for a compound with molecular formula C5H13N. Determine the structure of the compound. Any labile protons, if they exist, will not be present in this particular 1H NMR spectrum.
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
Complete the spectroscopy data tables for a compound with molecular formula C5H13N.
Determine the structure of the compound. Any labile protons, if they exist, will not be
present in this particular 1H NMR spectrum.

Transcribed Image Text:8) Complete the spectroscopy data tables for a compound with molecular formula C5H13N.
Determine the structure of the compound. Any labile protons, if they exist, will not be
present in this particular 1H NMR spectrum.
100
D
4000
3000
2000
ISDO
1000
S00
HAVENUMB ERI 1
1.90
f1 (ppm)
1.95
1.85
3.0 2.9
2.8
2.7
2.6
2.5
2.4
2.3
2.2
2.1 2.0
1.9 1.8 1.7
1.6 1.5 1.4
1.3 1.2 1.1 1.0
0.9
130 120 110 100
f1 (ppm)
90
80 70
60 50
40
30
20
10 0
TRANSHITTANCEI%I
Fooz
1.01.
5.98-
![8 Degrees of Unsaturation (show work):
DOU = 0
%3D
[2 (5) +2-13+1-0]
2.
1°C NMR Data Table
IR Data Table
Stretch (cm)
Bond
BC Signal Chemical Shift (ppm) PC Signal
> 3000 cm
H-N
44
C-H sp3
2
42ppam
~3000 cm'
26 ppm
4
23
'H NMR Data Table
'H Signal Chemical Shift (ppm) Integration
Multiplicity
to
A
2.75ppm
2H
Proposed Structure
1.90ppm
1.54ppm
2H
CH3
0.95ppm
6 H
H, N-C-C-CH3
CH3](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F41ea191e-828c-4f9d-b6fb-1ac8fc340597%2F43230cc6-1b09-4cd8-ae03-d72c3771e801%2Fo09zoem_processed.jpeg&w=3840&q=75)
Transcribed Image Text:8 Degrees of Unsaturation (show work):
DOU = 0
%3D
[2 (5) +2-13+1-0]
2.
1°C NMR Data Table
IR Data Table
Stretch (cm)
Bond
BC Signal Chemical Shift (ppm) PC Signal
> 3000 cm
H-N
44
C-H sp3
2
42ppam
~3000 cm'
26 ppm
4
23
'H NMR Data Table
'H Signal Chemical Shift (ppm) Integration
Multiplicity
to
A
2.75ppm
2H
Proposed Structure
1.90ppm
1.54ppm
2H
CH3
0.95ppm
6 H
H, N-C-C-CH3
CH3
Expert Solution

Step 1
Degree of unsaturation is 0
IR
3000 cm-1 due to Some C-H bond .
3300 cm-1 due to N-H bond .
NMR
0.9 6 H doublet
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