Carbohydrates Flashcards

1
Q

what are the functions of carbohydrates

A

energy and carbon source
energy store
flavouring
functional ingredient (gum, probiotics)

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2
Q

what are the 4 types of carbohydrate

A

monosaccharide
disaccharide
oligosacchardie
polysaccharides

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3
Q

outline the characteristics of monosaccharides

A
  • simple, one sugar unit
  • C3H6O3
  • aldoses and ketoses
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4
Q

what are the characteristics of aldoses

A

has a carbon and a double bonded oxygen at the end of the chain
contains an aldehyde group

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5
Q

what are the characteristics of ketoses

A

has a carbon and double bonded oxygen in the middle of the chain
contains a ketone group

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6
Q

define chiral

A

cannot be placed on top of its mirror image

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7
Q

examples of stereoisomers

A

D-…

L-…

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8
Q

what are the two chiral forms

A

enantiomers

epimers

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9
Q

what is an enantiomer

A

mirror reflection
compounds related by inverting the configuration at all asymmetric carbons
OH group pointing left = L-glucose
OH group pointing right= D-glucose

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10
Q

what is an epimer

A

disastereomers with an inverted configuration at one asymmetric carbon

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11
Q

what is a disastereomer

A

compounds related by inverting configuration at one or more chiral centres

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12
Q

what is meant by the cyclic structure of monosaccharides

A

reaction occurs between -OH at C-5 and the aldehyde at C-1, producing a pyranose ring
this produces an new asymmetric centre at C1, with two new alpha and beta stereoisomers- called anomers
alpha anomer- above the ring
beta anomer- below the ring
the anomie’s are interchangeable by mutarotation

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13
Q

give an example of a reducing sugar

A

all monosaccharides

glucose, fructose maltose, lactose

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14
Q

give examples of naturally occurring food monosaccharides

A

glucose, fructose, lactose, ribose

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15
Q

how is the anomeric carbon configuration determined

A

glucose

  • CH2OH and OH are on opposite sides on the anomeric carbon
  • 6 membered ring= pyranose

fructose

  • CHOH and OH are on the same side of the anomeric carbon
  • 5 membered ring= furanose
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16
Q

example of a disaccharide

A

maltose

17
Q

how are disaccharides formed

A

the hemiacetal end is free to open or close
the hemiacetal group of the alpha-delta-glucose reacts with the OH group of the beta-delta-glucose and forms a glycosidic bond

two monosaccharides formed by the glycosidic bond

18
Q

how is sucrose formed

A
glucose and fructose = sucrose
head to head
no free anomeric carbon so is non-reducing
inversion on heating
made by plants
19
Q

sugar beet is…

A

UK grown and processed in 6 factories

seasonal (Sept- March)

20
Q

sugar cane is…

A

a tropical plant that is shipped raw to the UK
processed all year in 1 UK factory
has many uses (flavour, colour, sweetener)

21
Q

how is lactose made

A

glucose and galactose
head to tail
reducing sugar

22
Q

give an example of a non-reading sugar

A

sucrose, trehalose

23
Q

how is trehalose made

A

glucose and glucose
head to head
energy storage in insects
non-reducing sugar

24
Q

what are polyols

A

sugar alcohols

25
Q

how are polyols produced and what are they used for

A

produced by the hydrogenation if sugars and syrups
used to replace sugars
fewer calories
small effect of blood glucose and insulin levels
non-cariogenic (no tooth decay)
in chewing gum, toothpaste

26
Q

what are oligosaccharides

A

3-10 covalently linked monosaccharides
found in artichokes, garlic, onions
e.g galactooligiosaccharide

27
Q

what are polysaccharides

A
10+ monosaccharides
homopolysaccharides
- single type of monomer
- straight or branched chain
- e.g starch and cellulose

heteropolysaccharides

  • two or more different monomers
  • straight or branches chain
  • e.g gellan gum