Which one of these four compounds would give a 13C NMR spectrum with only these three peaks, one at 210, one at 40 and one at 20 H₂C OB O 13C NMR delta (6) values C=O of ketones, aldehydes C=O of acids, esters, amides C=C and C=N C-X (where X = halogen, O) base position, alkyl C D OC A OA CH3 H3C B CH3 H₂C 220-200 160-180 100-150 40-70 0-40 CH3 H₂C D CH3
Which one of these four compounds would give a 13C NMR spectrum with only these three peaks, one at 210, one at 40 and one at 20 H₂C OB O 13C NMR delta (6) values C=O of ketones, aldehydes C=O of acids, esters, amides C=C and C=N C-X (where X = halogen, O) base position, alkyl C D OC A OA CH3 H3C B CH3 H₂C 220-200 160-180 100-150 40-70 0-40 CH3 H₂C D CH3
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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Transcribed Image Text:Which one of these four compounds would give a 13C NMR spectrum with only these three peaks, one at 210, one at 40 and one at 20?
H3C
OB
OD
13C NMR delta (8) values
C=O of ketones, aldehydes
C=O of acids, esters, amides
C=C and C=N
C-X (where X = halogen, O)
base position, alkyl C
OC
A
OA
CH3 H3C
B
CH3
H3C1
220-200
160-180
100-150
40-70
0 - 40
CH3
H₂C
D
CH3
Expert Solution

Step 1
13C NMR spectroscopy gives an idea of arrangement of carbon atoms in organic molecules. The number of peaks in the spectrum represents the number of sets of non equivalent carbon atoms in the molecule.
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