Organic Chemistry
Organic Chemistry
8th Edition
ISBN: 9781305580350
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher: Cengage Learning
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Chapter 14, Problem 14.30P

Following are mass spectra for the constitutional isomers 2-pentanol and 2-methyl- 2-butanol. Assign each isomer its correct spectrum.

Chapter 14, Problem 14.30P, Following are mass spectra for the constitutional isomers 2-pentanol and 2-methyl- 2-butanol. Assign , example  1

Chapter 14, Problem 14.30P, Following are mass spectra for the constitutional isomers 2-pentanol and 2-methyl- 2-butanol. Assign , example  2

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1B. Can 1H NMR spectroscopy be used to differentiate between the two compounds? Briefly explain why or why not. Predict the 1H NMR spectrum for each compound (include integration, multiplicity, and approximate chemical shift). Put it in data table format.
A common lab experiment is the dehydration of cyclohexanol to cyclohexene.(a) Explain how you could tell from the IR spectrum whether your product was pure cyclohexene, pure cyclohexanol,or a mixture of cyclohexene and cyclohexanol. Give approximate frequencies for distinctive peaks.
2) For each of the following pairs of compounds, name one absorption band that can be used to distinguish between them. State what the bond is (bond order, between which 2 atoms), and approximately where it appears in the IR spectrum (in cm ¹). b) HO 1-hexanol OH phenol H₂N 1-butanamine ethyl acetate cyclohexane OH hexanoic acid LOH cyclohexanol NH₂ butanamide diethyl ether cyclohexene

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