Draw the structure of a compound with the molecular formula C8H₁0 that exhibits five signals in its ¹3C NMR spectrum,four of which appear between 100 and 150 ppm.

Double Bond Equivalence (DBE) for the hydrocarbon having the molecular formula C8H10 can be…

Answered: Draw the structure of a compound with…

Draw the structure of a compound with the molecular formula C8H10 that exhibits five signals in its four of which appear between 100 and 150 ppm.

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter17: Carboxylic Acids

Section: Chapter Questions

Problem 17.17P

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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

Draw the structure of a compound with the molecular formula C8H₁0 that exhibits five signals in its ¹3C NMR spectrum,
four of which appear between 100 and 150 ppm.

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Compound 2 has molecular formula C6H12. It shows three signals in the 1H-NMR spectrum, one at 0.96 ppm, one at 2.03 ppm, and one at 5.33 ppm. The relative integrals of these three signals are 3, 2, and 1, respectively. Provide structure for compound 2, explain how you reached your conclusion.
Compound 1 has molecular formula C7H16. It shows three signals in the 1H-NMR spectrum, one at 0.85 ppm, one at 1.02 ppm, and one at 1.62 ppm. The relative integrals of these three signals are 6, 1, and 1, respectively. Compound 2 has molecular formula C7H14. It shows three signals in the 1H-NMR spectrum, one at 0.98 ppm, one at 1.36 ppm, and one at 1.55 ppm. The relative integrals of these three signals are 3, 2, and 2, respectively. Propose structures for compounds 1 and 2, explaining how you reach your conclusion.
A compound with molecular formula C3H8O produces a broad signal between 3200 and 3600 cm1 in its IR spectrum and produces two signals in its 1°C NMR spectrum. Draw the structure of the compound.
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