8. Given the ¹H NMR spectrum provided, give the structure of the molecule. The IR shows two strong peaksat 1750 cm¹ and 3400 cm¹. The molecular formula is C3H6O2. Integrations are given below.—|-101H9867Chemical Shift (ppm)1H52H32H2

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8. Given the 'H NMR spectrum provided, give the structure of the molecule. The IR shows two stróng peaks at 1750 cm' and 3400 cm'. The molecular formula is C3H6O2. Integrations are given below. | 10 1H 9 8 6 7 Chemical Shift (ppm) 1H 5 4 2H 2H 2

8. Given the 'H NMR spectrum provided, give the structure of the molecule. The IR shows two stróng peaks at 1750 cm' and 3400 cm'. The molecular formula is C3H6O2. Integrations are given below. | 10 1H 9 8 6 7 Chemical Shift (ppm) 1H 5 4 2H 2H 2

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter13: Structure Determination: Nuclear Magnetic Resonance Spectroscopy

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Problem 59GP: The mass spectrum and 13C NMR spectrum of a hydrocarbon are shown. Propose a structure for this...

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Mass Spectrometry

This process is an instrumental method in which a sample is changed to fast moving positive ions by electron bombardment. The charged particles vary due to their different mass to charge ratio and are estimated with the help of this difference. It is also called mass spectroscopy.

Question

8. Given the ¹H NMR spectrum provided, give the structure of the molecule. The IR shows two strong peaks
at 1750 cm¹ and 3400 cm¹. The molecular formula is C3H6O2. Integrations are given below.
—|-
10
1H
9
8
6
7
Chemical Shift (ppm)
1H
5
2H
3
2H
2

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