C10H13NO2 DOM 3284 IR Spectrum (KBr disc) 4000 100 لبلبلاء العليليليل 80 20 3000 40 13C NMR Spectrum (50.0 MHz, CDCI, solution) DEPT CH₂ CH₁ CHA proton decoupled 10 200 white... M+* 137 179 120 160 200 240 80 ¹H NMR Spectrum (200 MHz, CDCI, solution) exchanges with D₂O on warming 9 8 2000 108 1658 v (cm¹) m/e 160 1600 7 it expansion 120 (0) 6 1200 7.6 800 Mass Spectrum C10H13 NO2 5 280 solvent 80 7.0 ppm 4 3 UV Spectrum max 250 nm (log₁0 3.1) max 287 nm (log₁0€ 2.2) solvent: chloroform 40 2 0 8 (ppm) I 1 TMS 0 8 (ppm)

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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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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(f) C10H13NO2
4000
100
80
60
20
% of base peak
3284
43
3000
40
10
IR Spectrum
(KBr disc)
proton decoupled
13C NMR Spectrum
(50.0 MHz, CDCI, solution)
DEPT CH₂ CH₁ CH
200
9
80
¹H NMR Spectrum
(200 MHz, CDCI, solution)
exchanges
with D₂O on warming
108
le
137
M+*
179
120
160
2000
8
1658
v (cm¹)
1600
m/e
1
160
if
L
7
120
expansion
1200
6
200 240 280
7.6
800
Mass Spectrum
C10H13 NO₂
5
solvent
80
l
7.0
4
ppm
UV Spectrum
max 250 nm (log₁0€ 3.1)
A max 287 nm (log₁0 2.2)
solvent: chloroform
3
40
2
0
1
8 (ppm)
TMS
0
8 (ppm)
Transcribed Image Text:(f) C10H13NO2 4000 100 80 60 20 % of base peak 3284 43 3000 40 10 IR Spectrum (KBr disc) proton decoupled 13C NMR Spectrum (50.0 MHz, CDCI, solution) DEPT CH₂ CH₁ CH 200 9 80 ¹H NMR Spectrum (200 MHz, CDCI, solution) exchanges with D₂O on warming 108 le 137 M+* 179 120 160 2000 8 1658 v (cm¹) 1600 m/e 1 160 if L 7 120 expansion 1200 6 200 240 280 7.6 800 Mass Spectrum C10H13 NO₂ 5 solvent 80 l 7.0 4 ppm UV Spectrum max 250 nm (log₁0€ 3.1) A max 287 nm (log₁0 2.2) solvent: chloroform 3 40 2 0 1 8 (ppm) TMS 0 8 (ppm)
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