Amines Flashcards
Explain why amines are able to act as Bronsted-Lowry bases.
- Proton acceptor
- Lone pair of electrons in N is donated to H⁺
- Forming a dative covalent bond
BRONSTED-LOWRY BASE
Proton acceptor
Amines as Bases
amine + acid
amine + acid → ammonium salt
RNH₂ + HCl → RNH₃⁺Cl⁻
Preparation of Aliphatic Amines
halogenoalkane + excess ammonia
halogenoalkane + excess ammonia → amine + amonium salt
RCl + 2NH₃ → RNH₂ + NH₄⁺Cl⁻
Excess ethanolic ammonia
Reduction of Nitrobenzene
C₆H₅NO₂ + 6[H] → C₆H₅NH₂ + 2H₂O
Sn catalyst/conc. HCl/Reflux
Diazotisation: Reagents and Conditions
Reagents: NaNO₂/HNO₂/HCl
Conditions: Temp below 10°C
Diazotisation: Equation
C₆H₅NH₂ + HCl + HNO₂ → C₆H₅N⁺≡NCl⁻ + 2H₂O
Coupling with a Phenol: Reagents and Conditions
Reagents: NaOH
Conditions: Alkali
Coupling with a Phenol: Equation
C₆H₅N⁺≡NCl⁻ + C₆H₅OH → C₆H₅N=NC₆H₅OH + HCl