Problem 9 3458 6-H 3000 IR Spectrum 4000 znrl=3 300 2000 1600 1200 B00 v (cm') 100 Mass Spectrum Ho Gh 80 60 Mare blanch M 118 1SI No significant Uv 40 absorption above 220 nm 20- 103 CeH1402 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (100 O MH CDCI, solution) =14-14 =zaro DEPT CH CH, CHt proton decoupled solvent 200 160 120 80 40 8 (ppm) H NMR Spectrum (200 MHz. CDCI, solution) Exchanges with D20 TMS 6. 8. 5. 1. 98 wad ase 10

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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115
Problem 9
3458
R-H)
IR Spectrum
(CO soktiory
4000
zn+l=3
3000
2000
1600
1200
800
v (cm')
100
80
Mass Spectrum
60
Mate banch
M 118 1S)
40
No significant UV
absorption above 220 nm
20-
103
CeH1402
40
80
120
160
200
240
280
m/e
13C NMR Spectrum
(100 O MHz CDCI, solution)
-1-14
=zaro
DEPT CH CH, CH
proton decoupled
solvent
200
160
120
80
40
8 (ppm)
'H NMR Spectrum
(200 MHz. CDCI, solution)
Exchanges with
D20
TMS
9.
4.
3
8 (ppm)
98
ead aseps
10
Transcribed Image Text:115 Problem 9 3458 R-H) IR Spectrum (CO soktiory 4000 zn+l=3 3000 2000 1600 1200 800 v (cm') 100 80 Mass Spectrum 60 Mate banch M 118 1S) 40 No significant UV absorption above 220 nm 20- 103 CeH1402 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (100 O MHz CDCI, solution) -1-14 =zaro DEPT CH CH, CH proton decoupled solvent 200 160 120 80 40 8 (ppm) 'H NMR Spectrum (200 MHz. CDCI, solution) Exchanges with D20 TMS 9. 4. 3 8 (ppm) 98 ead aseps 10
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