1. For each spectral data set, determine the general type (C, CH, CH2, or CH) of each carbon signal.Are there any signals representing more than one carbon? How many degrees of unsaturation arethere in each formula?C3H16O214.0, q14.3, q17.1, q20.4, t36.0, t39.4, d60.0, t176.6, sb. CH10O354.1, q107.1, d131.2, dc. C;H16014.4, q16.6, q20.1, t35.5, t35.6, d68.3, ta.d. C,H850.2, d75.3, t143.3, d2. For each spectral data set in (1.) above, determine the general types of carbons (carbonyl, C=C_alkyl) for each "C NMR signal.

Formula for determining degree of unsaturation of a molecule Cn Hx Ny Oz = n - ( x/2 )…

Answered: 1. For each spectral data set,…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterL3: Carbon (13c) Nmr Spectroscopy

Section: Chapter Questions

Problem 14CTQ

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1Compound 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.
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.
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The question is attached..;
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