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13C NMR spectrum 20 180 160 140 120 100 80 60 40 20 CDS-00-327 ppm O singly substituted O para substituted O 1,4-Disubstituted O 1,2-Disubstituted O 1,3-Disubstituted O triply substituted

13C NMR spectrum 20 180 160 140 120 100 80 60 40 20 CDS-00-327 ppm O singly substituted O para substituted O 1,4-Disubstituted O 1,2-Disubstituted O 1,3-Disubstituted O triply substituted

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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
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Shown below are three isomers of a disubstituted benzene ring. The 1H NMR and 13C NMR spectra are also shown below for ONE of these isomers. Identify which isomer is producing these spectra? 

Hint: Consider the number of chemically equivalent hydrogen and carbon environments in each structure and the number of signals expected for each.

In practise, overlapping of signals may occur if two or more hydrogen environments (or carbon environments for 13C NMR) are very similar to one another. This is often seen for aromatic signals in particular.

13C NMR spectrum 200 180 160 140 120 100 80 60 40 20 CDS-00-327 ppm O singly substituted para substituted O 1,4-Disubstituted O 1,2-Disubstituted O 1,3-Disubstituted O triply substituted
Transcribed Image Text:13C NMR spectrum 200 180 160 140 120 100 80 60 40 20 CDS-00-327 ppm O singly substituted para substituted O 1,4-Disubstituted O 1,2-Disubstituted O 1,3-Disubstituted O triply substituted
Shown below are three isomers of a disubstituted benzene ring. The 'H NMR and 13C NMR spectra are also shown below for ONE of these isomers. Identify which isomer is producing these spectra? Hint: Consider the number of chemically equivalent hydrogen and carbon environments in each structure and the number of signals expected for each. In practise, overlapping of signals may occur if two or more hydrogen environments (or carbon environments for 1C NMR) are very similar to one another. This is often seen for aromatic signals in particular. CH3 CH CH. CH3 CH3 CH3 1,2-disubstituted 1,3-disubstituted 1.4-disubstituted 1H NMR spectrum 2 overlapping signals 9 8. 7 6 4 3. 2 1
Transcribed Image Text:Shown below are three isomers of a disubstituted benzene ring. The 'H NMR and 13C NMR spectra are also shown below for ONE of these isomers. Identify which isomer is producing these spectra? Hint: Consider the number of chemically equivalent hydrogen and carbon environments in each structure and the number of signals expected for each. In practise, overlapping of signals may occur if two or more hydrogen environments (or carbon environments for 1C NMR) are very similar to one another. This is often seen for aromatic signals in particular. CH3 CH CH. CH3 CH3 CH3 1,2-disubstituted 1,3-disubstituted 1.4-disubstituted 1H NMR spectrum 2 overlapping signals 9 8. 7 6 4 3. 2 1
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