27 Amines Flashcards
How to name amines
If primary amine , it means amine at the end of the chain
- this means can just name the chain
If secondary or tertiary and have the same alkyl group, then you can say di or tri amine
What if they’re two or more different functional alkyl groups whatever
First find the biggest chain, add that to the amine suffix
Then put N -and something each time to show what’s bonded, and do this in ALPHABETICAL ORDER
How can amines behave as bases
This is because with a. Lone pair on the N, they can react to add a hydrogen ion, and so as they can accept a proton, they are a BL base m dative covalent bind formed, and charge is + (conservation of charge)
Amines and acids
Amine and acids scoop fully up and becomes a salt
With + and - ions
How ti make an amine
Halolaken and EXCESS AMMONIA
Or haloalken and ammonia and NaOH
This is official way
Actual way and why
Here your adding ammonia to a haloalkane and then NaOH
You need to do this reaction using EXCESS AMMONIA, or else further substion if thr amine grouo may occur to make secondary and then tertiary structured
Also must do it through ethanol , otherwise with aqeuous the Halolakne might become into alchol with water by hydrolysis
Again what 2 conditions needed and why
Excess ammonia, so it doesn’t susbtjiure again
Ethanol, to prevent halolaken reacting. With water to make alchol
How ti make aromatic amine phenylamine
Starting from nitrobenzene, Sn/ Conc Hcl Wnd 6 hydrogens
To remmebe hydrogens, two waters must be produced so 4 hydrogens and 2 more left behind so 6 is needed
Reflux
Amino acid
Is a compound with bathe amine and Carboxyl group anywhere, r group and ch
As they have both Carboxyl and amine groups, they can react both ways
Amine groupnresctions
Amine acts as a base remember, thus it can react with acids
In this case, it becomes a protester molefule that’s it , become a protonated slat
Carboxylic acid reactions of amino acid
Gonna react with alkali to form a salt and water
Carbox esterificsrion amino acid?
Can also react with an schlock under sukfruic acid to form an ester .
This PROTONATED THE AMINE GROUP
Amides
CONH, made by acyl chrlodie reacting with ammonia / amine ti make amides, can also be the amine group and carboxylic acid groups of amino acids join in condensation polymerisation to form amide groups
Remember what is sterlisimerism
Dteroeisiomeriem is when it has the same Bernard and structural formula but different arrangement if atoms in space
Optical isomers are when two structured will have non superimposable mirror images of each other.
This is only possible through a chiral centre, WHICH IS A CARBIN WITH 4 DIFFERENT FUNCTIONSL GROUOS ATTACHED TO IT
often Lund in amino acids
As a result, the different enantiomers will have different properties, such a smell
How ti do condensation polymerisation
Two functional groups must be sued, with a loss of a small molecule each time
Here it can either be the same molefule with two different on each side, or two mooched with the same fucntinwl on each time, will have to rotatete each time