Chapter 27 Flashcards

(23 cards)

1
Q

What is an amine?

A

Derived from ammonia
One or more hydrogen atoms have been replaced by a carbon chain.

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

What is an aliphatic amine?

A

The nitrogen is attached to at least one carbon chain, straight or branched.

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

What is an aromatic amine?

A

The nitrogen is attached to at least one aromatic ring.

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

How do you name a primary amine where the amine group is at the end of the chain?

A

The prefix = alkyl group
Suffix = amine

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

How do you name a primary amine with the amine group in the middle of the chain?

A

Prefix = amino
Suffix = longest carbon chain

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

How do you name a primary amine with more than one amine group?

A

Prefix = di, tri amino
Suffix = longest carbon chain

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

How do you name a secondary or tertiary amine with the same R group?

A

Prefix = Di, Tri alkyl
Suffix = Amine

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

How do you name a secondary or tertiary amine with different R groups?

A

Largest chain = suffix, with amine
Shorter chains as N prefixes in alphabetical order

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

How do amines act as bases?

A

They have a lone pair of electrons on the nitrogen.
These can accept a proton and form Dative covalent bonds.
Neutralise acids to make salts.

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

How do you make primary aliphatic amines?

A

Ethanol as solvent.
Excess ammonia.
React the Haloalkane with ammonia and ethanol.

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

How do you make secondary and tertiary amines?

A

React the Haloalkane with the primary amine and ethanol.

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

How do you prepare aromatic amines?

A

Nitrobenzene reduced
Tin and HCl will act as the reducing agent

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

What are amino acids?

A

They contain amine and carboxylic acid functional groups.

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

What are the reactions of amino acids?

A

They react with acids to form a salt
They react with alkalis to form a salt
The carboxylic acid functional group can also be esterified by heating with an alcohol and a concentrated acid.

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

What is an amide?

A

A carboxylic acid derivative
The OH is replaced by NH2 or NHR’/NR’R’’

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

How do you name a primary amide?

A

Add the suffix amide

17
Q

How can you form an amide?

A

React ammonia with acyl chlorides, to form a primary amide.
React a primary amine with an acyl chloride to form a secondary amide.

18
Q

What is optical isomerism?

A

Molecules with a chiral centre
Non superimposable mirror images

19
Q

What is a chiral centre?

A

4 different groups around the carbon atom

20
Q

What is a condensation polymer?

A

The joining of monomers via a condensation reaction, with the elimination of a small molecule, usually water of hydrogen chloride.
Polyesters
Polyamides

21
Q

How can you form a polyester from one monomer?

A

The monomer needs to contain both the carboxylic acid and alcohol functional group.

22
Q

How are the monomers linked in a polyester?

A

An ester linkage