carbohydrates Flashcards

1
Q

empirical formula of carbohydrates

A

(CH2O)n

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2
Q

chirally active carbon

A

carbon is attached to 4 different groups

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3
Q

aldehyde carbon in aldoses

A

C1

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4
Q

carbonyl carbon in ketoses

A

C2

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5
Q

aldehyde

A

carbon is attached to hydrogen, r group and double bonded to oxygen

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6
Q

ketone

A

carbon attached to 2 r groups and double bonded to oxygen

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7
Q

3 carbon molecule

A

trioses

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8
Q

4 carbon molecule

A

tetroses

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9
Q

5 carbon molecule

A

pentoses

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10
Q

6 carbon molecule

A

hexoses

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11
Q

aldehyde + alcohol

A

hemiacetal

ring forms because r is part of same molecule as aldehyde

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12
Q

ketone + alcohol

A

hemiketal

ring forms because r is part of same molecule as the ketone

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13
Q

ring form of pyranose sugar structure

A

planar chair configuration

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14
Q

axial orientation

A

substituent points up or down

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15
Q

equatorial orientation

A

substituent is on the same plane as the ring

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16
Q

anomer

A

an epimer at the hemiketal/hemiacetal carbon = the anomeric carbon

17
Q

when the stereochemical isomer is at c1, is it a new sugar?

A

no, just an alpha or beta form of the sugar

18
Q

alpha and beta sugars

A

configuration (a or e) of anomeric carbon compared to anomeric reference atom.
eg in alpha it could be axial and beta it could be equatorial

19
Q

anomeric carbon in aldoses

A

C1

20
Q

anomeric carbon in ketoses

A

C2

21
Q

how are D and L sugars determined

A

configuaration of chirally active carbon furthest away from aldehyde or ketone groups

22
Q

enantiomer

A

mirror image molecules

23
Q

epimer

A

molecules are different sugars, asymmetric carbon 2,3,4 different configuration to glucose
you say epimers AT C_
eg glucose and mannose epimers at C4

24
Q

maltose

A

major product of starch digestion

hydrolysed by maltase

25
Q

lactose

A

sugar found in milk

hydrolysed by lactase

26
Q

sucrose

A

transported form of carbohydrate from plants

hydrolysed by sucrase

27
Q

starch and glycogen

A

polysaccharides of D-glucose

major energy source

28
Q

reducing end

A

terminal sugar where C1 is unattached

ring can open and aldehyde can form

29
Q

reducing sugar

A

any sugar capable of acting as a reducing agent because it has a free aldehyde or keto group

30
Q

cellulose structure

A

plant polysaccharide used for structure

long beta 1,4 glucose chains

31
Q

peptidoglycan

A

bacterial cell walls
good target for antibiotics
lysosome targets cell wall

32
Q

glycoconjugates

A

carbohydrates covalently linked to proteins and lipids

e.g. glycolipids

33
Q

o linked proteins

A

joined to hydroxyl of serine or threonine

34
Q

proteoglycans

A

attached mostly via O-linkage to glycosaminoglycans

adhesion of cells

35
Q

glycosyltransferases (GTs)

A

transfer sugars fro nucelotides onto other molecules