Primary amines give two N-H stretch peaks, one near 3350 and one near 3180, from asymmetric and symmetric vibrations respectively.
Secondary amines give one N-H stretch peak at 3300
N-H bending at 1640-1550 for both secondary and primary amides.
N-methyl acetamide |
Note how the C=O partially overlaps the N-H bend.
For dilute solutions the C=O is found at 1690. This is for the same reason as carboxylic acids - hydrogen bonding normally lowers the C=O frequency.
Like other carbonyl compounds, the C=O stretch frequency increases with decreasing ring size, by about 40 per carbon removed.
Did you just copy the figures out of Pavia Lampman Kriz and Vyvyan? I'm pretty sure that it is copywritten material.
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