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.
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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Get started for freeWould it be better to use 1H NMR or 13C NMR spectroscopy to distinguish 1-butene, cis-2-butene, and 2-methylpropene? Explain your answer.
Identify each compound from its molecular formula and itsNMR spectrum:
a)
b)
c)
How an NMR distinguish between the compounds in each of the following pairs?
a.
b.
c.
d.
e.
f.
g.
h.
i.
j.
Propose structures that are consistent with the following spectra. (Integral ratios are given from left to right across the spectrum.)
a. TheNMR spectrum of a compound with molecular formulahas two singlets with integral ratios of 2: 3.
b. TheNMR spectrum of a compound with molecular formulahas two singlets with integral ratios of 2: 3.
c. TheNMR spectrum of a compound with molecular formulahas two singlets with integral ratios of 1: 2.
a. Which proton or set of protons in each of the following compounds is the least shielded?
b. Which proton or set of protons in each compound is the most shielded?
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