Amines — Concept Maps
Jammu & Kashmir Board · Class 12 · Chemistry
4 concept maps of Amines for Jammu & Kashmir Board Class 12 Chemistry, each also written out as a text outline.
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Amines — Complete Concept Map
The map in words
- Amines
- Structure
- sp3 Hybridised N
- Pyramidal Shape
- Lone Pair on N
- Bond angle less than 109.5 deg
- Classification
- Primary 1 degree RNH2
- Secondary 2 degree R2NH
- Tertiary 3 degree R3N
- Alkylamines
- Arylamines
- Nomenclature
- Common name alkyl plus amine
- IUPAC alkanamine
- N dash locant for 2 degree 3 degree
- Aniline accepted IUPAC
- Preparation
- Reduction of Nitro Compounds
- Ammonolysis of Alkyl Halides
- Reduction of Nitriles LiAlH4
- Reduction of Amides LiAlH4
- Gabriel Phthalimide Synthesis
- Hoffmann Bromamide Degradation
- Physical Properties
- Lower amines are gases
- Fishy odour
- H bonding in 1 degree and 2 degree
- BP order 1 degree greater than 2 degree greater than 3 degree
- Solubility decreases with molar mass
- Chemical Reactions
- Basic Nature salts with acids
- Alkylation
- Acylation amides formed
- Carbylamine Test primary only
- Reaction with HNO2
- Hinsberg Test
- Electrophilic Substitution
- Basicity
- Alkylamines greater than NH3
- Arylamines less than NH3
- Aniline pKb 9.38
- Factors I effect solvation steric
- Diazonium Salts
- Diazotisation 273 to 278 K
- Sandmeyer Cl Br CN
- Gattermann Cl Br
- Balz Schiemann F only route
- KI for Iodo
- Hydrolysis for OH
- Coupling Azo Dyes
- Structure
Classification and Overview of Amines
The map in words
- Amines
- Structure
- sp3 hybridised N
- Pyramidal shape
- Lone pair on N
- Classification
- Primary 1 degree
- R-NH2
- Secondary 2 degree
- R2NH
- Tertiary 3 degree
- R3N
- Primary 1 degree
- Preparation
- Nitro compound reduction
- Ammonolysis of alkyl halides
- Nitrile reduction
- Amide reduction
- Gabriel synthesis
- Hoffmann degradation
- Physical Properties
- BP order
- Primary highest
- Secondary
- Tertiary lowest
- Solubility in water
- H-bonding
- BP order
- Chemical Reactions
- Basic character
- Alkylation
- Acylation
- Carbylamine test
- Reaction with HNO2
- Hinsberg test
- Electrophilic substitution
- Diazonium Salts
- Diazotisation
- Sandmeyer reaction
- Balz-Schiemann
- Coupling reaction
- Azo dyes
- Structure
Basicity of Amines in Aqueous Solution — The Three-Factor Analysis
The map in words
- Amine in Aqueous Solution
- Which factors operate?
- Inductive Effect
- More alkyl groups\nMore +I effect\nHigher electron density on N
- Favours Tertiary Amine
- Net Result in Water
- Methylamines Order
- Dimethylamine stronger\nthan Trimethylamine
- NOT simply Tertiary bigger than Primary
- Dimethylamine stronger\nthan Trimethylamine
- Ethylamines Order
- Diethylamine stronger\nthan Triethylamine
- Methylamines Order
- Net Result in Water
- Favours Tertiary Amine
- More alkyl groups\nMore +I effect\nHigher electron density on N
- Solvation Effect
- More N-H bonds\nBetter H-bonding with water\nConjugate acid more stable
- Favours Primary Amine
- More N-H bonds\nBetter H-bonding with water\nConjugate acid more stable
- Steric Hindrance
- Bulkier alkyl groups\nHinder water approach\nPoor solvation
- Disfavours Tertiary Amine
- Bulkier alkyl groups\nHinder water approach\nPoor solvation
- Inductive Effect
- Which factors operate?
Amines
The map in words
- Amines
- Definition and nature
- Classification
- Structure and geometry
- Nomenclature
- Methods of preparation
- Basic character
- Factors affecting basicity
- Physical properties
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