Propose a structure consistent with each set of spectral data assign each peak in the structure of your compound C5H10OIR peaks at 2950, 1720 (cm-1)1H NMR:2.6 (1H, septet)2.1 (3H, singlet)1.0 (6H, doublet)C4H8Br2:IR peak at 3000-2850 cm1H NMR:1.87 (singlet, 6 H)3.86 (singlet, 2 H)

1H proton shows different peaks for different types of hydrogen present in the organic compound. The…

Answered: C5H10O IR peaks at 2950, 1720 (cm-1) 1H…

C5H10O IR peaks at 2950, 1720 (cm-1) 1H NMR: 2.6 (1H, septet) 2.1 (3H, singlet) 1.0 (6H, doublet) C4H8Br2: IR peak at 3000-2850 cm-¹ 1H NMR: 1.87 (singlet, 6 H) 3.86 (singlet, 2 H)

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter12: Structure Determination: Mass Spectrometry And Infrared Spectroscopy

Section12.SE: Something Extra

Problem 48AP: The infrared spectrum of the compound with the mass spectrum shown below lacks any significant...

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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

Propose a structure consistent with each set of spectral data assign each peak in the structure of your compound

C5H10O
IR peaks at 2950, 1720 (cm-1)
1H NMR:
2.6 (1H, septet)
2.1 (3H, singlet)
1.0 (6H, doublet)
C4H8Br2:
IR peak at 3000-2850 cm
1H NMR:
1.87 (singlet, 6 H)
3.86 (singlet, 2 H)

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