Chapter 13: Q10P (page 408)
Draw structures for compounds that meet the following descriptions:
(a) C2H6O ; one singlet
(b) C3H7CI ; one doublet and one septet
(c) C4H8CI2O ; two triplets
(d) C2H8O ; one singlet, one triplet, and one quartet
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Chapter 13: Q10P (page 408)
Draw structures for compounds that meet the following descriptions:
(a) C2H6O ; one singlet
(b) C3H7CI ; one doublet and one septet
(c) C4H8CI2O ; two triplets
(d) C2H8O ; one singlet, one triplet, and one quartet
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Carboxylic acids react with alcohols (R'OH) in the presence of an acid catalyst. The reaction product of propanoic acid with methanol has the following spectroscopic properties. Propose a structure.

MS: = 88
IR: 1735
NMR: 1.11 (3 H, triplet, J 5 7 Hz); 2.32 (2 H, quartet, J 5 7 Hz); 3.65 (3 H, singlet) NMR: 9.3, 27.6, 51.4, 174.6
Suppose you ran a DEPT-135 spectrum for each substance in Problem
13-47. Which carbon atoms in each molecule would show positive
peaks, and which would show negative peaks?
Propose structures for compounds with the following formulas that show only one peak in their NMR spectra:
a.
b.
c.
Question: Predict the number of carbon resonance lines you would expect in the C- 13 NMR spectra of the following compounds:
(a) Methylcyclopentane
(b) 1- Methylcyclohexane
(c) 1,2- Dimethylbenzene
(d) 2- Methyl-2-butene
(e)

(f)

Predict the splitting patterns you would expect for each proton in the following molecules:
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