4000 100 80 لللللللللل 60 IR Spectrum (liquid film) 40 20 % of base peak 10 43 mum 1715 3000 40 C 75 LIE 101 M+ 132 '80 13C NMR Spectrum (20.0 MHz, CDCI, solution) proton decoupled 9 ¹H NMR Spectrum (100 MHz, CDCI, solution) 200 2000 1 8 V (cm¹) 1600 160 7 120 1200 120 160 200 240 280 m/e 6 Mass Spectrum 800 C-H 5 C6H1203 solvent 80 4 -CH3 3 No significant UV absorption above 220 nm H-C-H -CH3 40 2 TMS 0 1 8 (ppm) TMS f 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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Determine the structure of the compound using the information provided below, show the proton integration and the mass spectrometry fragments (ensure curly arrow mechanism). 

опанит
1715
1600
IR Spectrum
100
4000
(liquid film)
43
80
75
60
M
40
20
% of base peak
10
3000
40
C
13C NMR Spectrum
(20.0 MHz, CDCI solution)
proton decoupled
9
80
200
¹H NMR Spectrum
(100 MHz, CDCI, solution)
101
8
2000
v (cm¹)
M**
132
120 160
m/e
160
7
6
1200
120
Mass Spectrum
200 240 280
800
C-H
5
C6H1203
solvent
L
80
4
-CH3
No significant UV
absorption above 220 nm
3
H-C-H
u
-CH3
40
2
59
TMS
0
1
8 (ppm)
TMS
0
8 (ppm)
Transcribed Image Text:опанит 1715 1600 IR Spectrum 100 4000 (liquid film) 43 80 75 60 M 40 20 % of base peak 10 3000 40 C 13C NMR Spectrum (20.0 MHz, CDCI solution) proton decoupled 9 80 200 ¹H NMR Spectrum (100 MHz, CDCI, solution) 101 8 2000 v (cm¹) M** 132 120 160 m/e 160 7 6 1200 120 Mass Spectrum 200 240 280 800 C-H 5 C6H1203 solvent L 80 4 -CH3 No significant UV absorption above 220 nm 3 H-C-H u -CH3 40 2 59 TMS 0 1 8 (ppm) TMS 0 8 (ppm)
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