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)
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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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: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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