Carbohydrates 1 Flashcards

1
Q

What are carbs?

A

Carbon-based molecules with many hydroxyl groups

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

What are carbs used for?

A

Used for energy storage, cellular recognition

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

What are the horizontal bonds in fischer projection?

A

Project outwards

Wedge bonds

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

How do the vertical bonds project?

A

Backwards

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

What is a carbonyl group?

A

it is a Carbon double bonded to an O

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

What is an aldehyde?

A

A central carbon bonded to a R and H and double bonded to a O

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

Ketone

A

Same as aldehyde but instead of an H it is bonded to a diff R group

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

What are monosaccharides?

A

Aldehydes or ketones with two or more hydroxyl groups called aldoses or ketoses. 3-6 carbons

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

What are isomers?

A

Same molecular formula but diff structure

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

Constitutional isomer

A

Differ in the order of the atoms

Structural isomer

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

Stereoisomers

A

same order of atoms but diff spatial arrangement

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

What are the two stereoisomers?

A

Enantiomers and diasteremoers

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

Enantiomers

A

Nonsuperimposable mirror images

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

Diasteromers

A

Isomers that are not mirror images

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

What are the two types of diastereomers?

A

Epimers and anomers

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

Epimers

A

Differ at only one of several asymmetric carbon atoms

17
Q

Anomers

A

differ at a new asymmetic carbon formed on ring closure

18
Q

Can you have diastereomers that are neither epimers or anomers?

A

Yes

19
Q

How does ring closure work? (aldehydes)

A

Aldehyde and alcohol groups can react forming a hemiacetal

20
Q

What is a hemiacetal

A

A carbon attached to a R group, H group, OH, and OR

21
Q

What type of ring stend to be stable?

A

5 and 6 membered rings

22
Q

What is a 6 membered ring called?

A

Pyranose

23
Q

5 membered ring?

A

Furanose

24
Q

Why is chair conformation favoured?

A

bc there is less steric hindrance

25
Q

Is axial or eq better?

A

Eq bc axial has more steric hindrance

26
Q

How does ring closure work? (ketones)

A

Ketones and alcohol can react to from hemiketals

27
Q

Hemiketal

A

C attached to R, R’, OH, OR”