Carboxylic Acids + Derivatives Flashcards

1
Q

What are Carboxylic Acids?

A

Compounds with the Carboxyl (-COOH) functional group which has a carboxyl group (C=O) and a Hydroxyl Group (O-H)

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

How do you name Carboxylic Acids?

A

Find the longest carbon chain then adding ‘-oic acid’ on the end. Carboxyl group is always Carbon 1. The carboxyl group will always be at the end

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

Carboxylic Acids are weak acids. What does this mean?

A

They dissociate partially to form a H+ ion and a carboxylate ion and equilibrium lies to the left as it dissociates poorly

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

When they react with Carbonates (CO3 2-), What is formed?

A

Salt, Carbon Dioxide and water

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

Write the equation when ethanoic acid reacts with sodium carbonate?

A

2CH3COOH (Aq) + Na2CO3(s) –> 2CH3COONa + H2O + CO2

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

Write the equation when ethanoic acid reacts with sodium hydrogen carbonate?

A

CH3COOH + NaHCO3 –> CH3COONa + H2O + CO2

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

What are the 2 ways esters can be formed?

A
  • Reacting alcohols with carboxylic acids w/ sulphuric acid catalyst
  • Reacting alcohols with acid anhydrides
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How are esters named?

A

Named in 2 sections, first bit is from the alcohol (alkyl) and the second bit is from the carboxylic acid (oate)

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

Give some uses of Esters?

A
  • Perfumes + food flavourings
  • Solvents
  • Plasticisers
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Why are Esters good solvents?

A

Esters are polar molecules so other polar compounds will dissolve readily in esters. Also have low boiling points and evaporate easily. This makes them valuable in making glues

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

Why are Esters used as plasticisers?

A

Used to make plastics more flexible during polymerisation. They can leach out of the plastic over time and the plastic becomes brittle

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

Why are Esters used as perfumes + food flavourings?

A

Some esters have sweet smells such as pear drops.

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

Explain the process of Ester Hydrolysis

A

Esters can be hydrolysed (splitting using water) however it can be sped up using acid (acid hydrolysis) and a base hydrolysis

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

Explain the process of Acid Hydrolysis

A

Use dilute acid to split ester into a carboxylic acid and an alcohol. We can use sulphuric or hydrochloric acid and is conducted under reflux

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

What happens to equilibrium if more water is added?

A

Shifts right and more product is produced

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

Explain the process of Base Hydrolysis

A

Use dilute base to split ester into a carboxylate ion and an alcohol. We can use sodium hydroxide and is conducted under reflux.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What happends when u react glycerol (alcohol) and fatty acids (carboxylic acid)?

A

It produces an ester which makes fats and oil

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is an oil?

A

An ester

19
Q

Why do Vegetable oils have lower melting points and are liquid at room temperature?

A

They have unsaturated hydrocarbon chains that aren’t straight which means the chains cant pack together closely and hence they have lower van der waals forces

20
Q

What type of molecule is fat?

A

An ester

21
Q

Why do Animal Fats have higher melting points and are solids at room temperature?

A

They have saturated hydrocarbon chains that are straight and more uniform than oils which means the chains can pack together closer hence have much higher van der waal forces

22
Q

How do you make soap?

A

Hydrolyse animal fats or vegetable oils by heating with sodium hydroxide.

23
Q

How do you make bio diesels?

A

Vegetable oils can be converted into biodiesel by reactin oils with methanol and a potassium hydroxide as a catalyst

24
Q

What is Biodiesel?

A

Mixture of fatty acids made from methyl esters and can be made from rapeseed oil

25
Q

What are Acyl Chlorides?

A

Acid chlorides have the functional group (-COCl) which contains the acyl group (COCl)

26
Q

How are Acyl Chlorides named?

A

Finding longest carbon chain and adding ‘-oyl chloride’ at the end. Carbon on th acyl group is always carbon 1 and the acyl group will always be at the end of the molecule

27
Q

What do acyl chlorides react with and what happens?

A

Water, Ammonia, Alcohol, primary amines. In each reaction the Cl is substituted for either an oxygen or nitrogen

28
Q

What are Acid Anhydrides?

A

A molecule made from 2 carboxylic acids that are the same

29
Q

How are Acid Anydrides name?

A

They are named by knowing the carboxylic acid it is made from and removing the acid and anhydride on the end.

30
Q

What do Acid Anhydrides react with and what happens?

A

It reacts with water, ammonia, alcohol and primary amines. Very similar to acyl chlorides except they are less vigourous.

31
Q

What type of reacts do acid chlorides undergo?

A

Nucleophilic Addition – Elimination

32
Q

Why do Acid chlorides undergo nucleophilic addition-elimination?

A

Acid chlorides have a strong δ+ on the carbon which is susceptible to attack from nucleophiles. They have a strong δ+ as the oxygen and chlorine atoms are electronegative and draw electrons towards themselves

33
Q

What is Aspirin?

A

An ester made by reactin ethanoic anhydride or ethanoyl chloride and salicylic acid

34
Q

Why is ethanoic anhydride used instead of ethanoyl chloride in industry?

A
  • Safer as its less corrosive
  • Safer as it dsoesnt produce harmful HCl gas
  • Safer as it doesn’t react vigorously with water
  • Cheaper
35
Q

What are Amides?

A

Derivatives of carboxylic acids and have the functional group of –CONH2

36
Q

What is formed when ethanoyl chloride reacts with water?

A

Ethanoic acid + HCl

Vigorous reaction and white misty fumes of hydrogen chloride gas produced

37
Q

What is formed when ethanoyl chloride reacts with ammonia

A

Ethanamide + HCl

Vigorous reaction and white misty fumes of hydrogen chloride gas produced

38
Q

What is formed when ethanoyl chloride reacts with Methanol

A

Methyl ethanoate + HCl

Vigorous reaction and white misty fumes of hydrogen chloride gas produced

39
Q

What is formed when ethanoyl chloride reacts with Methyl amine?

A

N - Methyl ethanamide + HCl

Vigorous reaction and white misty fumes of hydrogen chloride gas produced

40
Q

What is formed when ethanoic anhydride reacts with water

A

2 ethanoic acids

41
Q

What is formed when ethanoic anhydride reacts with ammonia

A

Ethanamide and ethanoic acid

42
Q

What is formed when ethanoic anhydride reacts with methanol

A

Methyl ethanoate + ethanoic acid

43
Q

What is formed when ethanoic anhydride reacts with methylamine

A

N - methyl ethanamide + ethanoic acid