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)
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)
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
Determine the structure of the compound using the information provided below, show the proton integration and the mass spectrometry fragments (ensure curly arrow mechanism).

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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