Chapter 14: Q48P (page 669)
Draw a splitting diagram for the proton and give its multiplicity if
a. b.

Short Answer
a.

This has five peaks, called quintet.
b.

This has eight peaks i.e., double of quartet.
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Chapter 14: Q48P (page 669)
Draw a splitting diagram for the proton and give its multiplicity if
a. b.

a.

This has five peaks, called quintet.
b.

This has eight peaks i.e., double of quartet.
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Predict the splitting patterns for the signals given by compounds in Problem 4.
a. If two signals differ by 1.5 ppm in a 300 MHz spectrometer, by how much do they differ in a 500 MHz spectrometer?
b. If two signals differ by 90 Hz in a 300 MHz spectrometer, by how much do they differ in a 500 MHz spectrometer?
Dr. N. M. Arr was called in to help analyze the 1 H NMR spectrum of a mixture of compounds known to contain only C, H, and Br. The mixture showed two singlets-one at 1.8 ppm and the other at 2.7 ppm-with relative integrals of 1: 6, respectively. Dr. Arr determined that the spectrum was that of a mixture of bromomethane and 2-Bromo-2-methylpropane. What was the ratio of bromomethane to 2-Bromo-2-methylpropane in the mixture?
An alkyl halide reacts with an alkoxide ion to form a compound whose 1H NMR spectrum is shown here. Identify the alkyl halide and the alkoxide ion.

Draw a diagram like the one shown in Figure 14.12 to predict;
a. the relative intensities of the peaks in a triplet.
b. the relative intensities of the peaks in a quintet.
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