ORGANIC CHEMISTRY (LL) W/WILEYPLUS NEXT
ORGANIC CHEMISTRY (LL) W/WILEYPLUS NEXT
12th Edition
ISBN: 9781119664635
Author: Solomons
Publisher: WILEY
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Chapter 14, Problem 33P

Give a structure for compound F that is consistent with the 1 H NMR spectrum in Fig. 14.28 and IR absorptions at 3020, 2965, 2940, 2870, 1517, 1463, and 818 c m 1 .

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Compound K, molecular formula C6H14O, readily undergoes acid-catalyzed dehydration when warmed with phosphoric acid to give compound L, molecular formula C6H12, as the major organic product. The 1H-NMR spectrum of compound K shows signals at d 0.90 (t, 6H), 1.12 (s, 3H), 1.38 (s, 1H), and 1.48 (q, 4H). The 13C-NMR spectrum of compound K shows signals at d 72.98, 33.72, 25.85, and 8.16. Deduce the structural formulas of compounds K and L.
Give the structure that corresponds to the following molecular formula and H1 NMR spectrum:: C7H16O4: δ 1.93 (triplet); δ 3.35 (s); δ 4.49 (triplet); relative integral 1:6:1.
How could 1H NMR spectroscopy be used to distinguish among isomersA, B, and C?

Chapter 14 Solutions

ORGANIC CHEMISTRY (LL) W/WILEYPLUS NEXT

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NMR Spectroscopy; Author: Professor Dave Explains;https://www.youtube.com/watch?v=SBir5wUS3Bo;License: Standard YouTube License, CC-BY