Amines Flashcards
How can primary amines act as bases
- the lone pair of electrons on the nitrogen is readily available for forming a dative covalent bond with the H+ and accepting a proton
Why are primary amines stronger bases than ammonia
- The alkyl groups donate electron density to nitrogen
- so make the lone pair more readily available to accept a proton
Why are secondary amines stronger bases than primary
- They have more alkyl groups
- so more electrons are pushed to the Nitrogen
- so more positive inductive effect
- lone pair is more available to accept a proton
Why are aromatic amines the weakest bases
- if the N is attached to a benzene ring the lone pair on the nitrogen becomes partially delocalised into the ring
- so lone pair on Nitrogen is less available to accept a proton
What’s the overall order of base strength weakest to strongest
- aromatic amines (weakest)
- ammonia
- 1° amines
- 2° amines (strongest)
How do benzene rings bonded to nitrogen effect lone pair availability
Makes it less available so less likely to accept a proton so weaker base
Why is it better to prepare primary amines from nitriles compared to haloalkanes
- With haloalkane there is a further reaction but with nitriles there isn’t
- so with nitriles you get a single product and a higher atom economy
Describe number of alkyl groups in 1°, 2°, 3°,4° amines
Primary - 1 alkyl group
Secondary - 2 alkyl groups
Tertiary - 3 alkyl groups
Quarternary- 4 alkyl groups
What is the difference between aliphatic and aromatic amine
Aliphatic - without benzene
Aromatic - benzene
What are uses of amines
- dyes