Amines are organic compounds containing nitrogen with a lone pair, typically in the form –NH₂, –NHR, or –NR₂. This chapter is crucial for NEET as it covers classification, basicity, reactions, and electrophilic substitution in aromatic amines.
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STD 11 |
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1 |
Some Basic Concept Of Chemistry |
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2 |
Structure Of Atom |
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3 |
Classification Of Elements & Periodicity In Properties |
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4 |
Chemical Bonding & Molecular Structure |
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5 |
Thermodynamics & Thermochemistry |
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6.1 |
Equilibrium - I (Chemical Equilibrium) |
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6.2 |
Equilibrium - II (Icon Equilibrium) |
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7 |
Redox Reactions |
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8.1 |
Organic Chemistry Nomenclature Of Organic Compounds |
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8.2 |
Organic Chemistry Isomerism |
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8.3 |
Organic Chemistry Purification & Characterization |
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8.4 |
Organic Chemistry Reaction Mechanism |
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9 |
Hydrocarbon |
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10 |
P - Block Elements - I |
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STD 12 |
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1 |
Solution & Colligative Properties |
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Electrochemistry |
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3 |
Chemical Kinetics |
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4 |
D & F - Block Elements |
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5 |
Co-Ordination Chemistry |
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6 |
Haloalkanes & Haloarenes |
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7 |
Alcohol , Phenol & Ethers |
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8.1 |
Aldehydes & Ketones |
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8.2 |
Carboxylic Acids & Their Derivative |
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9 |
Amines |
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10 |
Biomolecules |
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P - Block Elements - ll |
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Definition: Organic derivatives of ammonia (NH₃) in which one or more hydrogen atoms are replaced by alkyl or aryl groups.
General Formula:
Primary amine (1°): R–NH₂
Secondary amine (2°): R–NH–R’
Tertiary amine (3°): R–N–R’₂
Importance: Amines are widely used in dyes, pharmaceuticals, and agrochemicals and frequently appear in NEET questions.
IUPAC Names: Based on longest carbon chain attached to nitrogen:
Primary amines: Suffix –amine (e.g., Ethanamine)
Secondary/tertiary amines: N-substituted (e.g., N-Methylethanamine)
Common Names: Used for simpler amines (e.g., Methylamine, Dimethylamine)
Based on Structure:
Aliphatic amines: R–NH₂, R–NHR’, R–NR’₂
Aromatic amines: Ar–NH₂ (e.g., Aniline)
Based on Substitution:
Primary (1°), Secondary (2°), Tertiary (3°)
Cyclic Amines: Nitrogen incorporated in rings (e.g., Piperidine)
Small amines are soluble in water due to hydrogen bonding
Higher amines have lower solubility due to increasing nonpolar alkyl chains
Boiling points: Primary > Secondary > Tertiary amines (except H-bonding exceptions)
Aromatic amines like aniline show weaker H-bonding due to delocalization of nitrogen lone pair
Basicity:
Lone pair on nitrogen accepts a proton → basic behavior
Aliphatic amines > Aromatic amines (aniline less basic due to resonance)
Reactions with Nitrous Acid (HNO₂):
Primary aliphatic amines → Alcohols (via diazonium intermediates)
Primary aromatic amines → Diazonium salts (important in dye chemistry)
Acylation and Alkylation:
Acylation forms amides
Alkylation can lead to over-alkylation forming tertiary amines
Electrophilic Substitution in Aromatic Amines:
Amino group is activating and ortho/para directing
Examples: Nitration of aniline, halogenation
Questions often involve basicity, reaction with nitrous acid, acylation, and aromatic substitution.
Amines appear in organic reaction mechanisms and industrial applications, making them high-yield for NEET.
Understanding structure-reactivity relationship is crucial for solving NEET questions efficiently.
Comparing basicity of aliphatic vs aromatic amines
Formation and reactions of diazonium salts
Electrophilic substitution reactions (e.g., nitration, halogenation)
Reactions with acyl halides forming amides
Alkylation reactions of primary amines
Memorize Nomenclature Rules – Primary, secondary, tertiary, aromatic amines
Practice Mechanisms – Diazotization, electrophilic substitution, acylation
Understand Physical Properties and Basicity Trends – Compare aliphatic vs aromatic amines
Refer NCERT Examples – NEET follows NCERT closely
Solve Previous Year Questions – Reinforces reaction mechanisms and product predictions
Mastering Amines is essential for NEET success. It allows students to predict reaction outcomes, understand basicity trends, and solve mechanism-based questions confidently. A strong understanding ensures high scoring potential in Class 12 organic chemistry.