Propose a reasonable structure based on the molecular formula, the H NMR, and the proton-decoupled 1C NMR data. The unknown compound has a molecular formula of C,HO and peaks with an * correspond to a CH, group by DEPT. H NMR 3H 8 H Draw the unknown compound. Select Draw Rings More Erase 2H C H (CH3)4 Si 2 H 1 H 3.5 3.0 2.5 2.0 1.5 1.0 0.5 0.0 300-MHz 'H NMR spectrum ppm (8) 13C NMR

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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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2 H
3.5
3.0
2.5
2.0
1.5
1.0
0.5
0.0
300-MHz 'H NMR spectrum ppm (8)
13C NMR
60
40
20
13C NMR spectrum ppm (8)
Transcribed Image Text:2 H 3.5 3.0 2.5 2.0 1.5 1.0 0.5 0.0 300-MHz 'H NMR spectrum ppm (8) 13C NMR 60 40 20 13C NMR spectrum ppm (8)
Propose a reasonable structure based on the molecular formula, the H NMR, and the proton-decoupled C NMR data. The
unknown compound has a molecular formula of C,HO and peaks with an * correspond to a CH, group by DEPT.
'H NMR
3 H
8 H
Draw the unknown compound.
Select
Draw
Rings
More
Erase
2 H
H
(CH3)4 Si
2 H
1 H
3.5
3.0
2.5
2.0
1.5
1.0
0.5
0.0
300-MHz 'H NMR spectrum ppm (8)
13C NMR
Transcribed Image Text:Propose a reasonable structure based on the molecular formula, the H NMR, and the proton-decoupled C NMR data. The unknown compound has a molecular formula of C,HO and peaks with an * correspond to a CH, group by DEPT. 'H NMR 3 H 8 H Draw the unknown compound. Select Draw Rings More Erase 2 H H (CH3)4 Si 2 H 1 H 3.5 3.0 2.5 2.0 1.5 1.0 0.5 0.0 300-MHz 'H NMR spectrum ppm (8) 13C NMR
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