1) For each of the compounds below tell how many signals you would expect the molecule to have in its normal, broadband decoupled 13C NMR spectra. A) C(CH3)4 C) C6H5-CH2-C6H5 в) р-Cl-C6H4-сн(сн3)2
1) For each of the compounds below tell how many signals you would expect the molecule to have in its normal, broadband decoupled 13C NMR spectra. A) C(CH3)4 C) C6H5-CH2-C6H5 в) р-Cl-C6H4-сн(сн3)2
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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Transcribed Image Text:1) For each of the compounds below tell how many signals you would expect the molecule
to have in its normal, broadband decoupled 13C NMR spectra.
A) C(CH3)4
C) C6H5-CH2-C6H5
B) p-CI-C6H4-CH(CH3)2
2) For three compounds, For each compound below tell how many types of nonequivalent
protons there are.
3) What is the splitting pattern for the hydrogens in 3-methyl-2-butanone(please labeled H
as a, b, c to answer one by one).
4) Treatment of tert-butyl alcohol with hydrogen chloride yields a mixture of tert-butyl
chloride (SN1 product) and 2-methylpropene (El product). After chromatographic
separation, how would you use 1H NMR to help you decide which was which?
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