IR Spectrum (liquid film) 4000 100 80 60 40 20 3000 40 10 13C NMR Spectrum (50.0 MHz, CDCI, solution) G 80 200 DEPT CH₂ CH₂ CH proton decoupled 9 101 129 LIJ M+ 174 120 ¹H NMR Spectrum (200 MHz, CDCI, solution) expansion 4.0 2000 8 1736 W v (cm¹) 160 1600 m/e 1 7 2.0 1200 160 200 240 280 1 120 t 6 Mass Spectrum ppm 800 5 C8H1404 solvent 80 1 4 L J 3 No significant UV absorption above 220 nm 40 1 2 08 (ppm) 1 1 TMS 1 0 8 (ppm)

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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Determine the structure of the compound using the information provided below, show the proton integration and the mass spectrometry fragments (ensure curly arrow mechanism).

IR Spectrum
(liquid film)
4000
100
80
60
40
20
3000
40
13C NMR Spectrum
(50.0 MHz, CDCI, solution)
10
الليسا
80
proton decoupled
¹H NMR Spectrum
DEPT CH₂ CH₂ CH
200
9
(200 MHz, CDCI, solution)
101
expansion
4.0
2000
8
1736
v (cm¹)
129
1600
solvent
160
120
80
40
11
2.0
ppm
120 160 200
m/e
M+
174
7
1200
1
6
800
Mass Spectrum
C8H1404
240 280
5
4
No significant UV
absorption above 220 nm
3
2
0 8 (ppm)
1
TMS
1
0
8 (ppm)
Transcribed Image Text:IR Spectrum (liquid film) 4000 100 80 60 40 20 3000 40 13C NMR Spectrum (50.0 MHz, CDCI, solution) 10 الليسا 80 proton decoupled ¹H NMR Spectrum DEPT CH₂ CH₂ CH 200 9 (200 MHz, CDCI, solution) 101 expansion 4.0 2000 8 1736 v (cm¹) 129 1600 solvent 160 120 80 40 11 2.0 ppm 120 160 200 m/e M+ 174 7 1200 1 6 800 Mass Spectrum C8H1404 240 280 5 4 No significant UV absorption above 220 nm 3 2 0 8 (ppm) 1 TMS 1 0 8 (ppm)
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