Ch. 4 Carbohydrates (Exam 1) Flashcards

Monosaccharides (Nomenclature & Ring Formation), Disaccharides (Glycosidic Bond Geometry), Polysaccharides (Linear & Branched), Carbohydrate Derivatives

1
Q

What is the empirical formula for a carbohydrate?

A

C(n)H(2n)O(n)

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2
Q

What functional groups do carbs consist of?

A

Hydroxyls and carbonyls

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3
Q

Are carbs water soluble?

A

Yes

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4
Q

What are carbs a good source of?

A

Rapid energy

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5
Q

What is the range of carbons in a monosaccharide?

A

3-8

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6
Q

Which sugars have aldehyde groups?

A

Aldoses

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7
Q

Which sugars have ketone groups?

A

Ketoses

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8
Q

How many carbonyls are in a monosaccharide?

A

1

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9
Q

What suffix denotes sugar?

A

-ose

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10
Q

How are monosaccharides named?

A

Based on number of carbons

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11
Q

What method is used to draw a monosaccharide?

A

Fischer projection

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12
Q

Which way does the OH group on the penultimate (next to last) carbon face for D stereochemistry?

A

Right

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13
Q

Which way does the OH group on the penultimate (next to last) carbon face for L stereochemistry?

A

Left

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14
Q

How do you decide the stereochemistry of a monosaccharide?

A

The penultimate (next to last) carbon with the OH group determines where stereochemistry will be L or D

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15
Q

Which carbon is the most oxidized?

A

C1 - the carbonyl/carbon at top of Fischer projection

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16
Q

Do most organisms metabolize L or D sugars?

A

D sugars

17
Q

What are epimers?

A

Epimers are sugars differing at different carbon atoms other than the D or L carbon

18
Q

What are 5 common types of monosaccharides discussed in the lecture?

A

1) Erythose
2) Ribose
3) Glucose
4) Galactose
5) Fructose

19
Q

How many carbons are needed to form a sugar ring?

A

5 or more

20
Q

What reactants are needed to form a hemiacetal/hemiketal (HINT: 2 key function groups)?

A

Carbonyl and hydroxyl (OH)

21
Q

What is an anomeric carbon, and what does it determine about a cyclic molecule?

A

The carbon that was the carbonyl in acyclic form and decides whether the sugar is in alpha or beta conformation in cyclic form

22
Q

How can you determine whether an anomeric carbon is in alpha or beta conformation?

A
  • Alpha: anomeric carbon faces up on same side of ring w/ 6th carbon
  • Beta: anomeric carbon faces down on opposite side of ring w/ 6th carbon
23
Q

What is the key difference between reducing and non-reducing sugars (HINT: something about the anomeric carbon)?

A

Reducing sugar: free anomeric sugar

Non-reducing sugar: no free anomeric sugar

24
Q

What are 2 examples of reducing sugars?

A

1) Maltose

2) Lactose

25
Q

What are 2 examples of non-reducing sugars?

A

1) Sucrose

2) Trehalose

26
Q

How do amylose molecules bond together?

A

Alpha 1,4 glycosidic bonds