Carbohydrates Flashcards

(40 cards)

1
Q

finish the sentence

Organic molecules are ones that contain …….

A
  • Carbon
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2
Q

What are monosaccharides?

A
  • Monosaccharides are the monomers from which larger carbohydrates are made
  • The single monomer (of sugar) ie. 1 sugar unit.

Monosacchardies = particular sugars

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3
Q

Give 3 examples of monosaccharides?

A

1.) Glucose
2.) Galactose
3.) Fructose.

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4
Q

How many isomers does glucose have, what are they?

A
  • 2 isomers
  • Alpha glucose
  • Beta glucose.
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5
Q

What is an isomer?

A
  • Isomer: same molecular formula but different structures.
  • Ie. alpha and beta glucose are both isomers of glucose.
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6
Q

What are disaccharides?

A
  • A pair of monosaccharides (ie. two sugar units.)
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7
Q

What are polysaccarides?

A
  • Many monosaccharides joined together.
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8
Q

3 examples of disaccharides.

A

1.) Sucrose.
2.) Maltose
3.) Lactose.

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9
Q

3 examples of polysaccharides.

A

1.) Starch.
2.) Cellulose.
3.) Glycogen.

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10
Q

What actually forms a glycosidic bond?

A
  • Condensation reaction between two monosaccharides forms a glycosidic bond.
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11
Q

How are disaccharides formed?

A
  • Disaccharides are formed by the condensation of two
    monosaccharides
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12
Q

What are maltose, sucrose and lactose examples of?

A
  • Maltose, sucrose and lactose are examples of dissacharides.
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13
Q

Give the word equation for the condensation reaction of maltose.

A

glucose + glucose —> maltose+ water

formed by the condesation of two glucose molecules.

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14
Q

Give the word equation for the condensation reaction of sucrose.

A

glucose + fructose –> sucrose + water

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15
Q

Give the word equation for the condensation reaction of lactose.

A

glucose + galactose –> lactose + water

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16
Q

How are polysaccharides formed?

A
  • Monosaccharides (ie. glucose units) joined together by glycosidic bonds that were formed from condensation reactions.
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17
Q

What monomer is starch made up of? How are the monomers joined together?

A
  • Many alpha glucose monosacharides join together by glycosidic bonds formed by condensation reactions.
18
Q

What type of glycosidic bonds are between the alpha glucose monosacharides/ monomers in amylose?

A

1-4 glycosidic bonds in amylose

Numbers show what part of molecule is bonded to other molecule (labelled numbers - sticky note on wall.)

19
Q

What type of glycosidic bonds are between the alpha glucose monosacharides/ monomers in amylopectin?

A

**1-4 and 1-6 **glycosidic bonds in amylopectin.

Numbers show what part of molecule is bonded to other molecule (labelled numbers - sticky note on wall.)

20
Q

What monomer is cellulose made up of?

21
Q

What type of glycosidic bond is between beta glucose monomers in cellulose?

A

1-4 glycosidic bonds.

22
Q

What type of glycosidic bond is between alpha glucose monomers in glycogen?

A

1-4 and 1-6 glycosidic bonds.

23
Q

Explain the hydrolysis of a disaccharide?

A
  • Water added to disaccharide.
  • Breaks/ hydrolyses glycosidic bond
  • Releases monosachrides
24
Q

Give the function of starch, glycogen and cellulose.

A
  • Starch: store of glucose
  • Glycogen: store of glucose.
  • Cellulose: Provides structural strength for the cell wall.
25
What organs is glycogen mainly found in?
- Muscle and liver cells.
26
Where is starch found?
- Plant cells.
27
# Finish the sentence Glycogen and starch are formed by the .......... of ........ ..........
- Condensation - alpha glucose
28
# Finish the sentence Cellulose is formed by the ........... of ....... ........
- Condensation. - Beta glucose.
29
What is the structure of starch?
- Mixture of two polysaccharides (bonded together) amylopectin and amylose. - Amylose: an unbranched helix (1-4 glycosidic bonds.) - Amylopectin: a branched molecule (1-4 glycosidic bonds AND 1-6 glycosidic bonds.) ## Footnote () - extra info for clarification
30
Explain how amylose's (polysaccharide in starch) structure allows it to carry out its function.
- Helix structure (helical) can compact to store a lot of glucose in a smaller place (ie. allowing for storage of glucose = function of starch.)
31
Explain how amylopectin's (component of starch) structure allows it to carry out its function.
- Branched molecule. - Increases surface area for enzymes to hydrolyse the glycosidic bond - allowing glucose to be released quickly FOR RESPIRATION!
32
How is starch's structure specially suited for its function of glucose storage?
- It is insoluble (does not affect water potential) so water is not drawn into cells by osmosis. - Compact. - The branches: large surface area: so enzymes can attach and hydrolyse the glycosidic bond (ie. for fast enzyme action.)
33
What is the structure of cellulose?
- Long, straight, unbranched chains - Chains are held in parallel by hydrogen bonds. - Hydrogen bonds between the chains form thick fibres called microfibrils (many cellulose chains .)
34
How is cellulose's structure specially suited for its function of providing structural strength to cell wall?
- Many hydrogen bonds provide collective strength. - Cellulose --> insoluble (won't affect water potential.)
35
What is the structure of glycogen?
- A highly- branched molecule
36
How is glycogen's structure specially suited for its function of glucose storage?
- Branched structure, more ends for faster hydrolysis/ enzyme action. - Branched so is compact. - Insoluble: won't affect water potential (water won't be drawn into cell --> cell won't burst ALONG WITH the glycogen.) - Glucose polymer so provides respiratory substrate for energy release. | () - extra info in own words for clarification
37
What makes a polysaccharide branched?
- Its 1-6 glycosidic bonds.
38
What is the -OH group on monosaccharides known as?
- Hydroxyl group.
39
What is it called in cellulose when every other glucose is rotated 180 degrees?
- They are **inverted. **
40
What is the advantage of glycogen, starch and cellulose being insoluble/ not affecting water potential?
- Water won't be drawn into cells that contain these molecules. - So the cells won't burst (along with the starch, cellulose and glycogen.)