C-NMR analysis on the molecule hexaphenylbenzene.

Principles of Instrumental Analysis
7th Edition
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Chapter19: Nuclear Magnetic Resonance Spectroscopy
Section: Chapter Questions
Problem 19.10QAP: Why is 133C-133C spin-spin splitting not observed in ordinary organic compounds?
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Help needed with the following C-NMR analysis on the molecule hexaphenylbenzene.

Note: we can assume the ispo carbons for the central ring are downfield of those of the subtitients. "Ipso" standing for the aromatic carbon to which a susbstituent is attached.

Thank you in advance!

40
39
34
33
41
38
35
32
NMR nuclei observed: C13
Solvent: CDC13
NMR field strength: 400 MHz
42
37
30
5
36
31
29
28,
27
4
7
22
23
26
2
3
8
15
10
9
16
12421
25
11
14
17
20
12
13
18
19
Transcribed Image Text:40 39 34 33 41 38 35 32 NMR nuclei observed: C13 Solvent: CDC13 NMR field strength: 400 MHz 42 37 30 5 36 31 29 28, 27 4 7 22 23 26 2 3 8 15 10 9 16 12421 25 11 14 17 20 12 13 18 19
140 130
T
120 110
100
90
(ppm)
76.98
77.12
77.26
127.67
127.90
129.22
133.41
134.60
80
PPM
60
50
40
Assignment
30
20
10
0
Transcribed Image Text:140 130 T 120 110 100 90 (ppm) 76.98 77.12 77.26 127.67 127.90 129.22 133.41 134.60 80 PPM 60 50 40 Assignment 30 20 10 0
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