The H-NMR spectrum of compound B, C7H140, consists of the following signals: 80.9 (t, 6H), 1.6 (sextet, 4H), and 2.4 (t, 4H). Draw the structural formula of compound B. • You do not have to consider stereochemistry. • Explicitly draw all H atoms. .

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
Chapter13: Nuclear Magnetic Resonance Spectroscopy
Section: Chapter Questions
Problem 13.27P: The 13C-NMR spectrum of 3-methyl-2-butanol shows signals at 17.88 (CH3), 18.16 (CH3), 20.01 (CH3),...
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) The H-NMR spectrum of compound B, C7H₁4 O, consists of the following signals: 8 0.9 (t, 6H), 1.6 (sextet, 4H), and 2.4 (t,
4H).
Draw the structural formula of compound B.
.
You do not have to consider stereochemistry.
Explicitly draw all H atoms.
.
Transcribed Image Text:) The H-NMR spectrum of compound B, C7H₁4 O, consists of the following signals: 8 0.9 (t, 6H), 1.6 (sextet, 4H), and 2.4 (t, 4H). Draw the structural formula of compound B. . You do not have to consider stereochemistry. Explicitly draw all H atoms. .
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