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Amines and Amides 1.7 Amines: Organic compounds of nitrogen N
Classified as primary, secondary, tertiary CH CH3 CH3—NH2 CH3—NH CH3—N — CH3 1° 2° °
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Naming Amines CH3CH2NH2 CH3—NH —CH3 ethanamine N-methylmethanamine NH2 | CH3CHCH3 Propan-2-amine aniline N-methyl aniline
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Learning Check AM1 Give the name and classify as primary, secondary or tertiary: A. CH3NHCH2CH3 CH3 | B. CH3CH2NCH3
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Solution AM1 A. CH3NHCH2CH3 N-methyl ethanamine, 2° CH3 | CH3CH2NCH3
N,N-dimethyl ethanamine 3°
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Alkaloids Physiologically active nitrogen-containing compounds
Obtained from plants Used as anesthetics, antidepressants, and stimulants Many are addictive
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Nicotine
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Caffeine
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Procaine
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Leaning Check AM2 Write a structural formula for Pentan-2-amine
B. cyclohexan-1,3-diamine
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Solution AM2 A. pentan-1-amine CH3CH2CH2CH2CH2-NH2 B. cyclohexan-1,3-diamine
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Amides Formed by the condensation reaction of an acid and an amine
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Naming Amides Alkanamide from acid name O methanamide (IUPAC) HC–NH2 propanamide (IUPAC) CH3CH2C–NH2
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Naming Amides with N-Groups
O CH3C–NHCH3 N-methylethanamide (IUPAC) CH3CH2C–N(CH3)2 N,N-dimethylpropanamide
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Learning Check AM3 Name the following amides: O A. CH3CH2CH2C–NH2 B. CH3C–N(CH2CH3)2
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Solution AM3 A. CH3CH2CH2C–NH2 butanamide B. CH3C–N(CH2CH3)2
N,N-diethylethanamide;
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Learning Check AM4 Draw the structures of A. Pentanamide B. N-methylbutanamide
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Solution AM4 A. Pentanamide O CH3CH2CH2CH2C–NH2
B. N-methylbutanamide CH3CH2CH2C–NHCH3
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