Class 12 Chemistry – Amines: Classification
1. Amines Overview
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Amines are derivatives of ammonia (NH₃) where one or more hydrogen atoms are replaced by alkyl or aryl groups.
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Functional group: –NH₂ (amine group)
2. Classification of Amines
a) Primary Amines (1°)
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Definition: One hydrogen of ammonia is replaced by an alkyl or aryl group.
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General Concept: R–NH₂
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Features:
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Contain one –NH₂ group attached to a carbon.
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Usually more reactive and basic.
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Example Concept: Methylamine
b) Secondary Amines (2°)
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Definition: Two hydrogens of ammonia are replaced by alkyl or aryl groups.
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General Concept: R–NH–R’
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Features:
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Contain one nitrogen bonded to two carbon atoms.
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Less basic than primary amines.
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Example Concept: Dimethylamine
c) Tertiary Amines (3°)
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Definition: All three hydrogens of ammonia are replaced by alkyl or aryl groups.
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General Concept: R–N–R’R’’
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Features:
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Nitrogen bonded to three carbon atoms.
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Least basic among aliphatic amines.
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Example Concept: Trimethylamine
d) Aromatic Amines
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Definition: Amines in which –NH₂ is attached to an aromatic ring (like benzene).
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General Concept: Ar–NH₂
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Features:
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Lone pair on nitrogen is delocalized into the ring, reducing basicity.
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Less reactive than aliphatic amines.
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Example Concept: Aniline
3. Quick Comparison Table
| Type | Nitrogen Attachment | Basicity | Reactivity | Example Concept |
|---|---|---|---|---|
| Primary (1°) | Nitrogen attached to 1 C | High | Most reactive | Methylamine |
| Secondary (2°) | Nitrogen attached to 2 C | Moderate | Less than 1° | Dimethylamine |
| Tertiary (3°) | Nitrogen attached to 3 C | Low | Least reactive | Trimethylamine |
| Aromatic | Nitrogen attached to benzene | Low | Less reactive | Aniline |
4. Key Points to Remember
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Primary, secondary, tertiary: Based on number of hydrogens replaced by carbon groups.
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Aromatic amines: Special case; nitrogen attached to benzene ring.
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Basicity trend (aliphatic): 1° > 2° > 3°
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Aromatic amines are less basic due to resonance delocalization.
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Amines are important in dyes, pharmaceuticals, and chemical synthesis.
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