π Key Concepts
Structure & Classification- Primary (RNHβ)
- Secondary (RβNH)
- Tertiary (RβN)
- Quaternary ammonium salts
Nomenclature- Common names
- IUPAC system
- Substituent priorities
β
π― Key Formulas
Key Reactions
- Preparation Methods
- Reduction of nitro compounds
- Gabriel phthalimide synthesis
- Hoffmann bromamide degradation
- Reduction of nitriles
- Ammonolysis of alkyl halides
- Chemical Reactions
- Basicity reactions
- Acylation
- Carbylamine reaction
- Diazotization
- Coupling reactions
- Alkylation
- Diazonium Salts
- Formation: ArNHβ + NaNOβ + HCl β ArNββΊClβ»
- Sandmeyer reaction
- Gattermann reaction
- Replacement reactions
β
β οΈ Common Mistakes to Avoid
Wrong order of basic strengthIncorrect identification of amine classMisunderstanding diazotization conditionsForgetting temperature control in diazonium formationWrong products in coupling reactionsβ
π Knowledge Prerequisites
Organic chemistry basicsFunctional group understandingAcid-base chemistryReaction mechanismsβ
π‘ Tips for Students
Master IUPAC nomenclatureUnderstand amine reactivityPractice diazonium salt reactionsβ
π Practice Recommedations
Solve structural identification problemsDraw reaction mechanismsCompare amine propertiesPredict chemical behaviorsβ
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