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)
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
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
![(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)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Faadfb7f9-0c88-4068-84aa-e612dc5261e2%2F1e3564a2-72b4-4e25-aebf-d57659538ff5%2F7pxrfyf_processed.png&w=3840&q=75)
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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