Each hydrogen of a primary amide typically has a separate 1H-NMR resonance, as

Chapter 18, Problem 18.15

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Each hydrogen of a primary amide typically has a separate 1H-NMR resonance, as illus-trated by the separate signals for the two amide hydrogens of propanamide, which fallat d 6.22 and d 6.58. Furthermore, each methyl group of N,N-dimethylformamide has aseparate resonance (d 3.88 and d 3.98). How do you account for these observations?

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