4) C11H1202 (Show the particular stereoisomer in this case) IR 13C NMR 100 ppm 166.82 144.52 134.54 130.19 128.88 128.06 118.37 60.41 14.34 1000 NAVENUME ERIal 200 180 160 140 120 1H NMR 100 80 60 40 20 CDS-00-726 ppm Assign. Shift(ppm) A 1.317 4.244 C 6.43 3 7.24 E 7.57 F 7.67 2 J(C,F) = 15.8HZ TMS 1 8 6 3 :-
4) C11H1202 (Show the particular stereoisomer in this case) IR 13C NMR 100 ppm 166.82 144.52 134.54 130.19 128.88 128.06 118.37 60.41 14.34 1000 NAVENUME ERIal 200 180 160 140 120 1H NMR 100 80 60 40 20 CDS-00-726 ppm Assign. Shift(ppm) A 1.317 4.244 C 6.43 3 7.24 E 7.57 F 7.67 2 J(C,F) = 15.8HZ TMS 1 8 6 3 :-
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
Please draw the structure of the molecule according to the nmr and it graph
![4)
C11H1202 (Show the particular stereoisomer in this case)
IR
13C NMR
L00
ppm
166.82
144.52
134.54
130.19
128.88
128.06
118.37
60.41
14.34
1000
RAVENUME ERIl
200
180
160
140
120
1H NMR
100
80
60
40
20
CDS-00-726
ppm
Assign. Shift(ppm)
A
1.317
4.244
C
6.43
3
7.24
7.57
F
7.67
2
J(C,F) = 15.8HZ
TMS
1
8
6
3
2](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F7a87b8d0-a46b-459a-ac98-f803ee812d98%2F5258bfcf-c4ef-432b-8ae5-e0a7ba394046%2Fpz8g1q8_processed.jpeg&w=3840&q=75)
Transcribed Image Text:4)
C11H1202 (Show the particular stereoisomer in this case)
IR
13C NMR
L00
ppm
166.82
144.52
134.54
130.19
128.88
128.06
118.37
60.41
14.34
1000
RAVENUME ERIl
200
180
160
140
120
1H NMR
100
80
60
40
20
CDS-00-726
ppm
Assign. Shift(ppm)
A
1.317
4.244
C
6.43
3
7.24
7.57
F
7.67
2
J(C,F) = 15.8HZ
TMS
1
8
6
3
2
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