3.3 carbohydtrates Flashcards

1
Q

What are the monomers in volved in making up carboydrates?

A

monosacharides

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2
Q

What are the two types of glucose molecules and their differneces and similatrities in structure?

A

Both hexose monosacaride
Alpha - H above the OH group on C1
Beta- OH group above H group on C1

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3
Q

give and example of a

hexose and pentose monosacarides

A

pentose: eg. ribose 5 carbons
Hexose: eg glucose 6 carbons

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4
Q

what elements make up

carbohydrates?

A

H O C

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5
Q

Monosacharides join to produce

A

disacharides or polysacharides

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6
Q

what bond holds monosacharides together

A

glycosidic (oxygen bridge)

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7
Q

what is the reaction of the synthesis of glycosidc bond called?

A

condenstation reaction

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8
Q

what reaction breaks the glycosidic bond

A

hydrolisis

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9
Q

Sugar is a general term for

A

di or poly sacarides

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10
Q

…………+……….—> maltose

A

a-glucose+a-glucose

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11
Q

…………+……….—> sucrose

A

a-glucose + fructose

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12
Q

…………+……….—>lactose

A

a or b-glucose + galactose

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13
Q

Starch
* function?
* structure?
* properties that make it suited to its function?
* two types and their properties and structure?

A

Starch
* energy storage in plants (excess glucose)
* made up of** a-glucose**
* insoluble: so wont swell due to osmosis
* - amylose: long, coiled and unbranched for compact sotorage, 1,4 gylcosidic bonds
* -amylopectin:long brancehed chain quick release because enzyme has more acsess points 1,4 glycosidic bonds and 1,6 glycosid bonds

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14
Q

Glycogen
* function?
* structure?
* properties that make it suited to its function?

A
  • energy storage in animals- excess glucose stored as glycogen
  • polysacaride of a-glucose 1,4 & 1,6 glycosid bonds
  • Very branched more than amylopectin- fast release of glucose for mobile animals
  • compact- good for storage
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15
Q

Celluslose
* function?
* structure?
* properties that make it suited to its function?

A
  • cell wall structure and support
  • long and unbranched alternating beta glucose with H-bonds between cellulose chains
  • strong microfibrils due to the additional H- bonds for further structural support
  • beta glucose alternating chain, hydrogen bonds between chains, microfibril, macrofibril, cellulose fibre
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16
Q

B-glucose vs A-glucose chains

A

Beta- OH group on top so chain is alternating every other monomer is flipped (180) upsidedown relative to neighbouring molecule
Alpha H group on top

17
Q

which sugars have reducing properties?

A

maltose and lactose

18
Q

which sugar has is non-reducing?

19
Q

explain when polymerised glucose forms cellulose and not starch

A

the hydroxly group on c1 is above the ring so alternate glucose molecules must rotate 180, so the hydroxyfrom c1 and c4 are close enough to react, when condensation takes place this forms glycosidic bonds the rotation of glucose molecules produces straight chain cellulose, the sahpe of alpha molecules that dont need to rotate 180 causes the starch to coil.