Oxidation of Food Flashcards

1
Q

Name six chemicals found in food.

A
Aldehydes
Ketones
Alcohols
Carboxylic acids
Fats
Oils
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What can happen to chemicals in food?

A

They can be oxidised by oxygen in the air, which spoils the food.

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

Between the alcohol and alkane with the same number of carbons, which has the higher boiling point?

A

Alcohol

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

What happens to the boiling points of alcohol as the number of carbons increase?

A

It increases.

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

Explain the difference in the bonding of alcohols compared to alkanes.

A

Alcohol molecules have a polar -O-H group, resulting in hydrogen bonding. The hydrogen bonds are much stronger compared to the London dispersion forces between alkane molecules. This means alcohols require more energy to separate, giving higher boiling points than alkanes.

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

How can alcohols be classed?

A

Primary, secondary and tertiary.

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

How many carbons are attached to the carboxyl group in a primary, secondary, and tertiary alcohol?

A

1, 2, 3.

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

What is a diol?

A

An alcohol with two hydroxyl groups.

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

What is an alcohol with three hydroxyl groups called?

A

Triol

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

Name a common triol.

A

Glycerol (propane-1,2,3-triol) - the alcohol part of fats and oils.

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

Why do diols and triols have high boiling points?

A

Due to strong hydrogen bonding between molecules.

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

What does it mean if a product has a higher oxygen : hydrogen ratio than the reactant?

A

Oxidation has taken place.

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

Can tertiary alcohols be oxidised?

A

No

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

What are primary alcohols oxidised to?

A

Aldehydes, and then oxidised again into carboxylic acids.

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

What can secondary alcohols be oxidised to?

A

Ketones

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

What can a carboxylic acid be reduced to?

A

The corresponding aldehyde and alcohol. The oxygen:hydrogen ratio decreases from acid to alcohol, indicating a reduction.

17
Q

What do carboxylic acids neutralise?

A

Bases, to form salts.

18
Q

What can salts of a carboxylic group be used as?

A

Preservatives in food and prevent the growth of mould.

19
Q

What is particularly susceptible to oxidation?

A

Oils

20
Q

What happens when food spoils, due to oxidisation?

A

Products are formed, some of which have an unpleasant smell and taste. These products can be oxidised further, at the double bonds, releasing volatile aldehydes which also smell.

21
Q

How is an oil of fat described when oxidised/spoiled?

A

Rancid

22
Q

What is used to reduce the oxidation of chemicals in food?

A

Antioxidants - they extend the shelf life of food.

23
Q

What does an antioxidant do?

A

Some react with the oxygen, while others prevent the formation of soapy tasting peroxides.

24
Q

Name a common antioxidant used in food.

A

Ascorbic acid (vitamin C)

25
Q

What is an isomer?

A

Molecules that have the same molecular formula but a different arrangement of atoms.

26
Q

What is chain isomerism?

A

The atoms are arranged in a completely different order resulting in branches.

27
Q

What is position isomerism?

A

The basic carbon skeleton remains unchanged but functional groups can be moved around.

28
Q

What similar chemical compounds exhibit isomerism?

A

Esters, aldehydes, ketones, alcohols, and carboxylic acids.

29
Q

Which molecules can’t have positional isomers, and why?

A

Aldehydes and carboxylic acids, because the functional group must always be on the end carbon.

30
Q

What is functional group isomerism?

A

Molecules that contain different functional groups.