Predict the splitting pattern (multiplicity) for the following molecule:

Describe the ¹H NMR spectrum you would expect for each of the following compounds, indicating the relative positions of the signals:

i.

How would the ¹H NMR spectra for the four compounds with molecular formula C₃H₆Br₂ differ?

Which of the following compounds gives a 1H NMR spectrum consisting of only a singlet, a triplet, and a pentet?

Predict the splitting pattern (multiplicity) for the following molecule:

Predict the multiplicity (the number of peaks as a result of splitting) and the chemical shift for each shaded proton in the following compounds.

(a)

(b)

Why is there no coupling between the a and c protons or between the b and c protons in the cis and trans alkenes shown in Figure 14.20?

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Predict the splitting patterns for the signals given by the compounds in Problem 4.

d.

Predict the splitting patterns for the signals given by the compounds in Problem 4.

c. CH₂=CCl₂