IR Spectrum (CCla solution) 4000 100 80 60 40 20 % of base peak 29 40 10 3000 57 13C NMR Spectrum (100.0 MHz, CDCI, solution) proton decoupled 9 DEPT CH₂ CH₂ CH 200 M 88 80 ¹H NMR Spectrum (200 MHz, CDCI, solution) elle 2.0 8 2000 120 r "Win V (cm¹) 160 expansion 1744 m/e 7 160 1600 1.0 200 6 120 1200 Mass Spectrum 800 ppm 240 280 5 C4H8O₂ solvent 80 4 3 No significant UV absorption above 220 nm 40 0 2 [[ 8 (ppm) 1 TMS 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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Given the following NMR data, find the unknown compound. 

a. Identify the molecular formula; find IHD
b. Identify the 1H and 13C NMR signals

IR Spectrum
(CCla solution)
4000
100
80
60
40
20
% of base peak
29
40
10
3000
57
13C NMR Spectrum
(100.0 MHz, CDCI, solution)
proton decoupled
9
DEPT CH₂ CH₂ CH
200
M 88
80
¹H NMR Spectrum
(200 MHz, CDCI, solution)
elle
2.0
8
2000
120
r "Win
V (cm¹)
160
expansion
1744
m/e
7
160
1600
1.0
200
6
120
1200
Mass Spectrum
800
ppm
240 280
5
C4H8O₂
solvent
80
4
3
No significant UV
absorption above 220 nm
40
0
2
[[
8 (ppm)
1
TMS
0
8 (ppm)
Transcribed Image Text:IR Spectrum (CCla solution) 4000 100 80 60 40 20 % of base peak 29 40 10 3000 57 13C NMR Spectrum (100.0 MHz, CDCI, solution) proton decoupled 9 DEPT CH₂ CH₂ CH 200 M 88 80 ¹H NMR Spectrum (200 MHz, CDCI, solution) elle 2.0 8 2000 120 r "Win V (cm¹) 160 expansion 1744 m/e 7 160 1600 1.0 200 6 120 1200 Mass Spectrum 800 ppm 240 280 5 C4H8O₂ solvent 80 4 3 No significant UV absorption above 220 nm 40 0 2 [[ 8 (ppm) 1 TMS 0 8 (ppm)
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