Construct a simulated proton-decoupled C NMR spectrum for tert-butyl alcohol. Drag the resonance signal icon to the appropriate chemical shift positions. Then label the box above each resonance signal with the corresponding number of equivalent carbons. (Not all chemical shift bins will be used.) OH 220 200 180 160 140 120 100 80 60 40 20 8 (ppm) Answer Bank 2C 3C 1C

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Construct a simulated proton-decoupled C NMR spectrum for tert-butyl alcohol. Drag the resonance signal
icon to the appropriate chemical shift positions. Then label the box above each resonance signal with the
corresponding number of equivalent carbons. (Not all chemical shift bins will be used.)
OH
220
200
180
160
140
120
100
80
60
40
8 (ppm)
Answer Bank
2C
3C
1C
20
Transcribed Image Text:Construct a simulated proton-decoupled C NMR spectrum for tert-butyl alcohol. Drag the resonance signal icon to the appropriate chemical shift positions. Then label the box above each resonance signal with the corresponding number of equivalent carbons. (Not all chemical shift bins will be used.) OH 220 200 180 160 140 120 100 80 60 40 8 (ppm) Answer Bank 2C 3C 1C 20
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