4.1.4- Amines Flashcards
How are primary aliphatic amines prepared
In a nucleophilic substitution reaction of halogenoalkanes with excess ammonia (reagent) and ethanol as the solvent (condition) and warming (condition) (Not reflux as Ammonia gas would escape!)
Why are amines organic bases
Due to their ability to accept a proton (H+) due to the lone pair of electrons on the nitrogen which can form a dative covalent bond
What are the conditions for preparing aromatic amines
Mixture of tin, concentrated hydrochloric acid (act as the reducing agent: [H]) and heating under reflux
How are aromatic amines prepared
By reducing nitroarenes eg. Nitrobenzene.
What are the two steps in the synthesis of Azo-dyes
Diazoisation (formation of the diatonic ion) and then coupling.
How is the nitrous acid formed
In a mixture of sodium nitrite and hydrochloric acid:
NaNO2 + HCl -> HNO2 + NaCl
Give the reaction and condition for diazoisation
C6H5NH2 + HNO2 + HCl -> C6H5N+(Cl-)N (benzenediazonium chloride)+ 2H2O
Below 10°C
Give the reaction and condition for coupling
CC6H5N+(Cl-)N (benzenediazonium chloride) + phenol (or other aromatic compound eg. Amine) + NaOH -> the Azo-dye (C6H5-N=N-C6H4-OH) + NaCl + H2O
Alkaline conditions.