what is an amine
draw out what primary, secondary and tertiary amines would look like
why can amines accept H+
and in what conditions
it can form a dative covalent bond
in low ph conditions (acidic)
what are amines described as and why
bases as they can accept H+
weak base
what is the prefix for amines when there is another functional group on the molecule
amino
name this molecule
2-aminoethanoic acid
suffix for when amine is the only functional group on the molecule
amine
e.g. methyl amine
when do you put an N in front of a part of a molecule with an amine
put N in front of the smaller chain
what happens when you react a haloalkane and excess ammonia
nucleophilic substitution
forming a primary amine and hydrogen halide
what happens when you react a haloalkane and excess primary amine
forms a secondary amine and HCL
show the mechanism for a haloalkane and primary amine reaction
what are the 3 ways to synthesise amines
Haloalkane + NH3
Haloalkane and primary amine
make nitrile then reduce it
what is the best way to synthesise amines
make nitrile then reduce it (add lots pf H’s)
what must the conditions and method for synthesising an amine by making a nitrile then reducing it
add haloalkane with on less H than you want
add KCN (spectator K+) in acid
this nitrile reacts with [H]
using hydrogen and nickel catalyst
to form an amine
show an example of a mechanism to turn chloroethane into propanyl amine
how to turn nitrobenzene into a phenyl amine (and water)
reduce it using [H] and a tin catalyst
show the step by step synthesis of aromatic amines
how to add a nitrile onto benzene
react with HNO3 and H2SO4
why is at least one of the groups coming off the N on amines a carbon chain
if there was 3 H’s then it would be ammonia
what are the 2 main reactions of amines
lone pair accepts H+
amines are nucleophile
why do both of the reactions of amines occur
because of 1 lone pair of electrons on nitrogen
therefor it attacks as a base
show the synthesis of a secondary amine using a primary amine as a nucleophile
show the other reaction using amine as a nucleophile
how the reaction that occurs when amines are put in low and high pH
switches between amine and amine with hydrogen on it