100 80 60 4000 20 Wown 2114 3295 IR Spectrum (oud) 40 proton decoupled 2H 10 3C NMR Spectrum (100 MHz, CDC, solution) 3000 ¹H NMR Spectrum (400 MHz, CDC, solution) 25 55 200 I 9 182 80 1 8 2000 M-83 120 V (cm) 2H L 160 expansion 1600 C₂H₂N 160 200 240 280 m/e DEPT CH, CH, CH 1 20 1 7 1H 1200 6 120 Mass Spectrum 2H 800 1.5 5 solvent L L 80 1 exchanges with DO 4 2H 3 No significant UV absorption above 220 m 40 2 113 08 (ppm) 1 TMS 1 L 0 ō (ppm) IR: List bands and possible/probable structural units responsible Band (cm³) Possible stretches/functional groups MS: Molecular Formula 13C NMR: 1 2 3 4 5 6 Chem. Shift (8) Type of C (sp), sp², carbonyl, etc.) ¹H NMR: 1 IHD(DU)= Chem. Shift (8) Multiplicity (singlet, doublet, etc.) 2 3 4 5 6 If you need more space, add any additional signal info here: (Show calculation) # of attached H's #of identical C's in signal Probable Type of H (methyl, aromatic, etc.) #of identical H's in signal

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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3296
IR Spectrum
(quid film)
.......
wwwddd
4000
100
80
60
40F 8
-28
20
40
proton decoupled
10
13C NMR Spectrum
(100 MHz, CDC, solution)
2H
-
3000
¹H NMR Spectrum
(400 MHz, CDC, solution)
55
200
2.5
9
80
82
2114
8
2000
M = 83
120
V (cm-¹)
2H
L
160
expansion
1600 1200
C₂H₂N
160 200 240 280
m/e
DEPT CH, I CH₂ 1 CH 1
2.0
I
7
1H
6
L
120
Mass Spectrum
2H
1.5
800
5
solvent
I
80
exchanges
with DO
4
2H
L
3
No significant UV
absorption above 220 nm
|||
L
40
2
113
08 (ppm)
1
1
TMS
0
8 (ppm)
IR: List bands and possible/probable structural units responsible
Band (cm³)
Possible stretches/functional groups
MS:
Molecular Formula
13C NMR:
1
2
3
4
5
6
¹H NMR:
1
Chem. Shift (8) Type of C (sp, sp2²,
carbonyl, etc.)
2
Chem. Shift (8) Multiplicity (singlet,
doublet, etc.)
IHD(DU)=
3
4
5
6
If you need more space, add any additional signal info here:
(Show calculation)
of attached c
# of attached H's
# of identical C's in
signal
Probable Type of H
(methyl, aromatic, etc.)
# of identical H's
in signal
Transcribed Image Text:3296 IR Spectrum (quid film) ....... wwwddd 4000 100 80 60 40F 8 -28 20 40 proton decoupled 10 13C NMR Spectrum (100 MHz, CDC, solution) 2H - 3000 ¹H NMR Spectrum (400 MHz, CDC, solution) 55 200 2.5 9 80 82 2114 8 2000 M = 83 120 V (cm-¹) 2H L 160 expansion 1600 1200 C₂H₂N 160 200 240 280 m/e DEPT CH, I CH₂ 1 CH 1 2.0 I 7 1H 6 L 120 Mass Spectrum 2H 1.5 800 5 solvent I 80 exchanges with DO 4 2H L 3 No significant UV absorption above 220 nm ||| L 40 2 113 08 (ppm) 1 1 TMS 0 8 (ppm) IR: List bands and possible/probable structural units responsible Band (cm³) Possible stretches/functional groups MS: Molecular Formula 13C NMR: 1 2 3 4 5 6 ¹H NMR: 1 Chem. Shift (8) Type of C (sp, sp2², carbonyl, etc.) 2 Chem. Shift (8) Multiplicity (singlet, doublet, etc.) IHD(DU)= 3 4 5 6 If you need more space, add any additional signal info here: (Show calculation) of attached c # of attached H's # of identical C's in signal Probable Type of H (methyl, aromatic, etc.) # of identical H's in signal
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