Propose a reasonable structure based on the molecular formula, the 'H NMR, and the proton-decoupled 1BC NMR data. The unknown compound has a molecular formula of C,H0 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 C (CH3)4 Si 2H 1H 3.5 3.0 2.5 2.0 1.5 1.0 0.5 0.0 300-MHz 'H NMR spectrum ppm (8) C NMR
Propose a reasonable structure based on the molecular formula, the 'H NMR, and the proton-decoupled 1BC NMR data. The unknown compound has a molecular formula of C,H0 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 C (CH3)4 Si 2H 1H 3.5 3.0 2.5 2.0 1.5 1.0 0.5 0.0 300-MHz 'H NMR spectrum ppm (8) C NMR
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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Question
![1 H
3.5
3.0
2.5
2.0
1.5
1.0
0.5
300-MHz 'H NMR spectrum ppm (8)
0.0
13C NMR
20
40
60
13C NMR spectrum ppm (8)
Question Source: Organic Chemistry: Structure And F](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F82fa8a34-7954-4708-9bd1-5850213e0700%2Fba203aaf-01d0-4faf-ab99-083a1b9c6f29%2Fp66an76_processed.jpeg&w=3840&q=75)
Transcribed Image Text:1 H
3.5
3.0
2.5
2.0
1.5
1.0
0.5
300-MHz 'H NMR spectrum ppm (8)
0.0
13C NMR
20
40
60
13C NMR spectrum ppm (8)
Question Source: Organic Chemistry: Structure And F
![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,H0 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
2H
C
(CH3)4 Si
2 H
1H
3.5
3.0
2.5
2.0
1.5
1.0
0.5
0.0
300-MHz 'H NMR spectrum ppm (8)
BC NMR
Question Source: Organic Chemistry: Structure And Function 7e Publisher: W.H. Freema](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F82fa8a34-7954-4708-9bd1-5850213e0700%2Fba203aaf-01d0-4faf-ab99-083a1b9c6f29%2Fao4tai9_processed.jpeg&w=3840&q=75)
Transcribed Image Text: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,H0 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
2H
C
(CH3)4 Si
2 H
1H
3.5
3.0
2.5
2.0
1.5
1.0
0.5
0.0
300-MHz 'H NMR spectrum ppm (8)
BC NMR
Question Source: Organic Chemistry: Structure And Function 7e Publisher: W.H. Freema
Expert Solution
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Step 1
The molecular formula of the organic compound given is C7H16O.
The degree of unsaturation = C+1−(H/2)
where
C = number of carbon atoms
H = number of hydrogen atoms
The degree of unsaturation = 7+1−(16/2) = 8 − 8 = 0.
The degree of unsaturation zero indicates no multiple bonds or rings present in the structure.
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