Carbohydrates Flashcards

0
Q

What is a carbohydrate?

A

A carbohydrate is a molecule which contains carbon, hydrogen and oxygen only.

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

What is a organic molecule?

A

An organic molecule is a molecule containing two or more carbon atoms.

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

What are the main functions of a carbohydrate? Give examples.

A

To provide energy to do work in a cell. e.g glucose

To act as an energy store for later use. e.g starch (plants) and glycogen (animals)

Structural functions. E.g cellulose in plant cell walls and chitin in the exoskeletons of an insect.

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

What are the three structural levels of carbohydrates?

A

Monosaccharides.

Disaccharides.

Polysaccharides.

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

What are monosaccharides? Give an example.

A

These are simple sugars such as glucose.

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

What are disaccharides? Give an example.

A

These consist of two monosaccharides covalantly bonded together. E.g maltose.

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

What are polysaccharides? Give examples.

A

Also known as complex carbohydrates these consist of large numbers of monosaccharides bonded together such as starch and cellulose.

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

Give the name of each monosaccharide according to the number of Carbon atoms from three to six. Giving examples and formulas where appropriate.

A

3 - Triose’s : C3-H6-O3

4 - Tetrose’s : C4-H8-O4

5 - Pentose’s : C5-H10-O5 e.g Ribose sugar in RNA not DNA

6 - Hexose’s : C6-H12- O6 e.g Glucose

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

What are the general characteristics of monosaccharides?

A

Water soluble.

Are white crystals in a solid state.

Are sweet tasting.

Reduce Benedicts reagent (the copper sulphate component) to form a brick red precipitate.

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

What is the general formula for a hexose monosaccharide and where are they most common?

A

C6-H12-O6

These are the most common sugars in biological molecules.

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

There are many structural isomers of hexose sugars, what are the two simplest isomers?

A

The two types of Glucose, alpha and Beta.

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

How do alpha and beta glucose differ from each other?

A

In alpha the hydrogen on the C1 is above the hydroxyl group.

In Beta the hydrogen is below.

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

Name the three most common hexose sugars in biological molecules.

A

Glucose.

Fructose.

Galactose.

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

Outline the structure and features of galactose.

A

Is a hexose sugar with an almost identical structure to beta glucose apart from the hydrogen on the C4 carbon is also below the hydroxyl group.

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

Outline the structure and features of fructose.

A

Is a hexose sugar with a four carbon atoms in its ring and two outside it one group attached to the C1 carbon and another on the C5 carbon.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

The formulas for monosaccharides are part of a homologous series. What is this formula?

A

(C-H2-O)n

Where “n” is the number of carbon atoms.

21
Q

What are D and L isomers?

A

D and L carbohydrate isomers are mirror images of each other and are also known as optical isomers or enantiomers as they have the ability to bend light.

22
Q

What is the Valancy of an element?

A

The number of bonds an atom can make.

23
Q

What are the characteristics of disaccharides?

A

The same as monosaccharides except they don’t reduce Benedicts reagent apart from maltose.

24
Q

How are disaccharides formed?

A

Through a condensation reaction between two hydroxy groups, one on the C1 carbon and one on the C4 of the other monosaccharide. Forming a 1-4 glycosidic link and producing a single molecule of water.

25
Q

Explain how are disaccharides broken apart, giving an example.

A

The reverse reaction is called hydrolysis whereby the monosaccharides are separated through the addition of water. For example the hydrolase enzyme amylase in the mouth breaks down starch into units of maltose in the first stage of its metabolic pathway.

26
Q

What are hexose disaccharides in relation to each other?

A

Structural isomers with the general formula C12-H22-O11. (2(C6-H12-O6)-(H2-O))

27
Q

What is maltose constructed out of?

A

A combination of two glucose molecules.

28
Q

What is sucrose constructed out of?

A

Glucose and fructose.

29
Q

What is lactose constructed of?

A

Glucose and galactose.

30
Q

Why do monosaccharides and disaccharides dissolve in water?

A

This is because their free hydroxyl groups are able to form hydrogen bonds with water.

31
Q

What are the characteristics of polysaccharides?

A

They are insoluble, do not taste sweet, do not reduce Benedicts solution and are insoluble.

32
Q

What are the two types of starch molecule?

A

Amylose (20%) and Amylopectin (80%).

33
Q

What is the structure of amylose?

A

Amylose is constructed of between 200 and 5000 alpha glucose molecules which form an unbranched helical chain whose turns are bonded together by hydrogen bonds. (6 alpha glucose molecules to a turn) which is tightly coiled making it difficult for hydrolase enzymes to break it down as a result amylose releases its energy slowly. The resulting tube has closed ends with the hydroxyl groups inside making it inert and insoluble in water.

34
Q

Give two examples of where starch is found?

A

Plant tubers and in seed endosperm where it is found as granules.

35
Q

Describe the structure of amylopectin.

A

Is constructed of between 5000 and 100000 alpha glucose molecules which form a branched helical chain due to the presence of both 1-4 and 1-6 glycosidic links. Again this is an inert and insoluble molecule.

36
Q

Describe the structure of glycogen.

A

It is very similar to amylopectin apart from it has looser coils making it easier to access it’s energy and making the glycogen granules smaller than starch granules as they don’t stick together as well. As the coil isn’t as tight it is partially soluble in water.

37
Q

What is the reason for forming a insoluble energy store?

A

To conserve energy because if the glucose was left in its soluble form energy would be needed to stop it leaving by diffusion and to throw water out to prevent osmotic bursting.

38
Q

Describe the structure of a cellulose molecule.

A

This is constructed of about 15000 Beta glucose so the glycosidic links alternate with each other rather than forming a linear plane Like starch and glycogen.

39
Q

Describe the structure of a microfibril.

A

This consists of about 2000 linear cellulose molecules held together by very large numbers of hydrogen bonds and are about 20nm wide.

40
Q

Describe the properties of cellulose.

A

It has high tensile strength

Is insoluble due to hydrogen bonds between its hydroxyl groups.

41
Q

Describe the structure of a cell wall.

A

This consists of a middle lamella made of pectic compounds such as pectin which is a polymer of about 200 galacturonic acid molecules on top of which the cellulose microfibrils are mounted in a gel-like matrix. There is then a secondary layered wall made of cellulose, hemicellulose and lignin.

42
Q

What is the function of a cell wall?

A

To protect the cell inside and to help it resist osmotic bursting when placed in pure water. Also to give support to plant cells and therefore the whole plant this is especially important for structures like leaves which would fold in on themselves if these walls weren’t present.

43
Q

How can cellulose be broken down.

A

Cellulose can be broken down by cellulase enzymes in ruminating herbivores (lateral chewing) such as cows.