27 Amines Flashcards

1
Q

How to name amines

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What if they’re two or more different functional alkyl groups whatever

A

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 well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How can amines behave as bases

A

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)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Amines and acids

A

Amine and acids scoop fully up and becomes a salt

With + and - ions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

How ti make an amine

A

Halolaken and EXCESS AMMONIA

Or haloalken and ammonia and NaOH

This is official way

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Actual way and why

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Again what 2 conditions needed and why

A

Excess ammonia, so it doesn’t susbtjiure again

Ethanol, to prevent halolaken reacting. With water to make alchol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How ti make aromatic amine phenylamine

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Amino acid

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Amine groupnresctions

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Carboxylic acid reactions of amino acid

A

Gonna react with alkali to form a salt and water

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Carbox esterificsrion amino acid?

A

Can also react with an schlock under sukfruic acid to form an ester .
This PROTONATED THE AMINE GROUP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Amides

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Remember what is sterlisimerism

A

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 well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

How ti do condensation polymerisation

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Okay remember how ti do it if they have two DIFFERENT MOLEFULES with dual ducntij al grouos

A

They join and it becomes (2n-1) H2O

How to show it, basically just remove a part of the molecule from each side that will in total ADD TO FORM THE WATER OR OR HCL
This often means removing Oh from one side of the cabroxykic acid , and just H from alchol, so be warry

17
Q

Remember base hydrokysisndiffernce compared to acid

A

Base will return the cabroylic acid as AN ION
So if done with NaOH, just realise the Na+ will stick to the cabroylic

But the alchol ALWAYS COMES BACK, or thr amine