Carbohydrates Flashcards

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1
Q

What are carbohydrates?

A

Polymers

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2
Q

What are the monomers of carbohydrates called and give some examples?

A

Monosaccharides.
e.g. typically sugars :
glucose, fructose, galactose

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3
Q

How is glucose useful?

A

Used in cellular respiration to make ATP ; using oxygen alongside.

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4
Q

What happens when you combine two monosaccharides give some examples.

A

You make a disaccharide.
e.g. sucrose, maltose, lactose

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5
Q

What is the name for many monosaccharides?

A

A polysaccharide

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6
Q

How are disaccharides formed?

A

They are formed from two monosaccharides joined together by a glycosidic bond formed by a condensation bond.

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7
Q

What are the equations for the 3 known disaccharides?

A

glucose + glucose —> maltose + water
glucose + galactose —> lactose + water
glucose + fructose —-> sucrose + water

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8
Q

What type of glycosidic bonds are disaccharides formed from?

A

1-4 glycosidic bond ( bond between carbon 1 and carbon 4)

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9
Q

What catalyses hydrolysis in the body?

A

Enzymes

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10
Q

During which process are carbohydrates hydrolysed into the body as monomers?

A

Glycogenolysis - store of glycogen hydrolysed back into glycogen when blood sugar levels drop.
Digestion - when starch is hydrolysed into glucose

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11
Q

How are carbohydrates important to an organism, the structure, and function of its cells?

A

To make cells through cellulose, fungi use it to make cell walls through chitin.

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12
Q

What is starch?

A

Starch is used as an energy store in plant cells. It is a polysaccharide of a - glucose.
Structure : Amylase - 1,4 glycosidic bonds —> unbranched
Amylopectin - 1,4 and 1,6 glycosidic bonds —–> branched.

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13
Q

What is glycogen?

A

Glycogen is used as an energy store in animal cells. It is a polysaccharide made of a-glucose. It has 1,4 and 1,6 - glycosidic bonds —-> branched.

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14
Q

How does the structure of starch ( amylase) relate to its function?

A

Starch ( amylase ) has a helical structure, making it compact for cell storage.
It is a large, insoluble polysaccharide molecule, can’t leave the cell / cross-cell membrane
Insoluble in water, the cell’s water potential is not affected ( no osmotic effect ).

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15
Q

How does the structure of glycogen ( and starch amylopectin ) relate to its function?

A

It is branched, making it compact/ to fit more molecules in a small area.
Branched, more ends for faster hydrolysis - release glucose for respiration to make ATP for energy release.
Large, insoluble polysaccharide molecules, cant leave cell / cross-cell membranes.
Insoluble in water, water potential of cell not affected ( no osmotic effect ).

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16
Q

What is cellulose?

A

Provides strength and structural support to plant/algae cell walls.
It is a polysaccharide of beta-glucose.
1,4 glycosidic bond —> straight, unbranched chains.
Chains are linked in parallel by hydrogen bonds forming microfibrils.

17
Q

How does the structure of cellulose relate to its function?

A
  • Every other beta-glucose molecule is inverted in a long, straight, unbranched chain.
  • Many hydrogen bonds link parallel strands ( crosslinks ) to form microfibrils ( strong fibrils).
  • Hydrogen bonds are strong in high numbers.
  • So provides strength to plant cell walls.
18
Q

Describe the test for reducing sugars.

A

Reducing sugars = monosaccharides, maltose, lactose
1. Add Benedict solution ( blue ) to the sample.
2. Heat in a boiling water bath.
3. Positive result = green/yellow/orange/red precipitate.

19
Q

Describe the test for non-reducing sugars.

A

Non-reducing sugars = sucrose.
1. Do Benedict’s test and stays blue/negative.
2. Heat in a boiling water bath with acid ( to hydrolysed into reducing sugars ).
3. Neutralise with alkali ( e.g. sodium bicarbonate ).
4. Heat in a boiling water bath with Benedict’s solution.
5. Positive result =green/yellow/orange/red precipitate.

20
Q

Suggest a method to measure the quantity of sugar in a solution.

A
  • Carry out the Benedict’s test as above, then filter and dry precipiate.
  • Find mass/weight.
21
Q

Describe the biochemical test for starch.

A

Add iodine dissolved in potassium iodide (orange/brown) and shake/stir
Positive result = blue/black.