15. Draw the structure for the compound at the bottom of the page. Show your reasoning IR Spectrum (iqeld fim 1715 4000 3000 2000 1600 1200 0.0 800 v (om") 100- 43 Mass Spectrum 0.5 80 UV spactrum 1.0 M 134 salvent : cyclohexane 7.00 mg / 10 mis path langth:0.50 om C3H100 1.5 40 80 120 160 200 240 280 200 250 300 2 (nm) 350 m/e 13C NMR Spectrum (50.0 MHz, CDCI, solution) DEPT CHt CHt CH profon decouplad salveni 200 160 120 8 (ppm) 80 40 1H NMR Spectrum (200 Mz, CDCI, colution) 5H 2H 3H TMS 10 3 *Spectra from "Organic Structures from Spectra", Field, Sternbell and Kalman 1 8 (ppm) Kof beae pask absorbance
15. Draw the structure for the compound at the bottom of the page. Show your reasoning IR Spectrum (iqeld fim 1715 4000 3000 2000 1600 1200 0.0 800 v (om") 100- 43 Mass Spectrum 0.5 80 UV spactrum 1.0 M 134 salvent : cyclohexane 7.00 mg / 10 mis path langth:0.50 om C3H100 1.5 40 80 120 160 200 240 280 200 250 300 2 (nm) 350 m/e 13C NMR Spectrum (50.0 MHz, CDCI, solution) DEPT CHt CHt CH profon decouplad salveni 200 160 120 8 (ppm) 80 40 1H NMR Spectrum (200 Mz, CDCI, colution) 5H 2H 3H TMS 10 3 *Spectra from "Organic Structures from Spectra", Field, Sternbell and Kalman 1 8 (ppm) Kof beae pask absorbance
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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
Transcribed Image Text:15. Draw the structure for the compound at the bottom of the page. Show your reasoning
IR Spectrum
(lquld fim)
1715
4000
3000
2000
1600
1200
0,0
800
V (om)
100
43
Mass Spectrum
80
0.6
60
UV spactrum
40
1.0
Mt
134
Balvent : cyclohexane
7.00 mg/10 mls
palh langth:0.5o am
20
CgH100
1.5
40
80
120
160
m/e
200
240
280
200
250
300
350
2(nm)
13C NMR Spectrum
(50.0 MHz, CDCI, solution)
DEPT CHat CH,t CHt
prolon decoupled
aclvent
200
160
120
80
40
8 (ppm)
H NMR Spectrum
(200 MHz, CDCI, colution)
5H
2H
3H
TMS
10
8
4
2
*Spectra from "Organic Structures from Spectra", Field, Sternbell and Kalman
0.
8 (ppm)
% of base peak
absorbance
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