Carbohydrates Flashcards

(25 cards)

1
Q

What is a carbohydrate?

A

A compound of carbon and water; the most common biomolecule, used for energy, storage, and structural roles.

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

What are Lewis structures?

A

Straight-line covalent bond diagrams with dots for unpaired electrons.

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

What is a Fischer projection?

A

A simple way to depict isomers, commonly used for carbohydrates.

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

What is a Haworth projection?

A

A 3D-like projection useful for visualizing carbohydrates in ring form.

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

What is a chair conformation?

A

A model showing the actual spatial structure of a molecule; more detailed but can be confusing.

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

How are carbohydrates named by carbon number?

A

3 C → Triose

4 C → Tetrose

5 C → Pentose

6 C → Hexose

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

How are carbohydrates named by functional group?

A

Aldehyde → Aldose

Ketone → Ketose

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

Example of aldohexose and ketohexose?

A

Aldohexose → Glucose

Ketohexose → Fructose

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

What does the suffix “-ose” mean?

A

It indicates a sugar.

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

What are enantiomers?

A

Isomers that are mirror images.

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

What are diastereomers?

A

Isomers with more than one chiral center that are not mirror images.

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

What are epimers?

A

Isomers differing at only one chiral center.

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

Example of D- and L- configurations?

A

D-tetrose (with aldehyde group, 4 C, 2 chiral centers → 4 stereoisomers) has D- and L- forms as enantiomers.

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

How many stereoisomers for a sugar with 4 chiral centers?

A

16 stereoisomers (8 D, 8 L; 8 enantiomer pairs).

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

What increases carbohydrate stability?

A

Cyclization:

6-membered ring → pyranose

5-membered ring → furanose

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

What are anomers?

A

Cyclic monosaccharide epimers that differ at the anomeric carbon.

17
Q

What’s the difference between α and β anomers?

A

α (alpha): OH on anomeric C opposite side of O (trans)

β (beta): OH on anomeric C same side as O (cis)

18
Q

What type of reaction forms a glycosidic bond?

A

A condensation reaction (dehydration reaction).

19
Q

What are examples of disaccharides?

A

Maltose = glucose + glucose

Lactose = glucose + galactose

Sucrose = glucose + fructose

20
Q

What is the most abundant organic compound?

21
Q

Why does the body store glucose as glycogen?

A

Because glycogen is insoluble in water, making it a compact, efficient storage form.

22
Q

What is the base unit of chitin?

A

N-acetyl-β-D-glucosamine.

23
Q

How can carbohydrates be chemically modified?

A

By redox reactions or addition of functional groups (e.g., phosphate, amino, N-acetyl).

24
Q

What is the general formula of carbohydrates?

25
What are key roles of carbohydrates?
Provide structure, energy, and form glycosidic bonds.