From the h nmr and c nmr of the unknown carbonyl compound determine its structure and draw it, label each c, ch, ch2, or ch3 group using letters (a,b,c) and assign each peak in the proton and carbon nmr spectrum to the carbons and hydrogens that correspond to it in the molecule.Example of what should be included in the table:hydrogen/carboncarbon chemical shifthydrogen chemical shiftsplitting patternintegralcouples to CDC13240122201120010QE-300180916081401206100LO3~0Carbonyl Compound A: C3H60 100-98-96-94929088-86-8482-80-78-76-74-72-70-400035003366.930002932.532873.282-methyl-2-pertanol25002000Wavenumbers (cm-1)15001461.311376.581260.35155.861091.73987.211000912.06856.65800.99742.59500

The question is based on the concept of organic spectroscopy. We need to analyse the spectral data…

Answered: Carbonyl Compound A: C3H60 |4Q QE-300 2…

Chemistry: An Atoms First Approach

2nd Edition

ISBN:9781305079243

Author:Steven S. Zumdahl, Susan A. Zumdahl

Publisher:Steven S. Zumdahl, Susan A. Zumdahl

Chapter21: Organic And Biological Molecules

Section: Chapter Questions

Problem 142CWP

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From the h nmr and c nmr of the unknown carbonyl compound determine its structure and draw it, label each c, ch, ch2, or ch3 group using letters (a,b,c) and assign each peak in the proton and carbon nmr spectrum to the carbons and hydrogens that correspond to it in the molecule.

Example of what should be included in the table:

hydrogen/carbon	carbon chemical shift	hydrogen chemical shift	splitting pattern	integral	couples to

CDC13
240
12
220
11
200
10
QE-300
180
9
160
8
140
120
6
100
LO
3
~
0
Carbonyl Compound A: C3H60

100-
98-
96-
94
92
90
88-
86-
84
82-
80-
78-
76-
74-
72-
70-
4000
3500
3366.9
3000
2932.53
2873.28
2-methyl-2-pertanol
2500
2000
Wavenumbers (cm-1)
1500
1461.31
1376.58
1260.35
155.86
1091.73
987.21
1000
912.06
856.65
800.99
742.59
500

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