carbohydrates Flashcards

monosaccharides, disaccharides, polysaccharides

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1
Q

define monomer and polymer. Give some examples

A
  • monomer - smaller units that join together to form larger molecules - monosaccharides, amino acids, nucleotides
  • polymer - molecules formed when many monomers join together - polysaccharides, proteins, DNA/RNA
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2
Q

name the elements found in carbohydrates, lipids, proteins and nucleic acids

A

carbohydrates and lipids - CHO
proteins - CHONS
nucleic acids - CHONP

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2
Q

why happens in a condensation and hydrolysis reaction

A

condensation: chemical bond forms between 2 molecules and a molecule of water is produced
hydrolysis - a water molecule is used to break a chemical bond between 2 molecules

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3
Q

describe the properties of alpha glucose

A

small and water soluble - easily transported in bloodstream
complementary shape to antiport for co-transport for absorption in gut
complementary shape to enzymes for glycolysis - respiratory substrate

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4
Q

what type of bond forms when monosaccharides react

A

1,4 or 1,6 glycosidic bond
2 monomer = 1 chemical bond = disaccharide
multiple monomers = many chemical bonds = polysaccharides

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5
Q

name three disaccharides. describe how they form

A

maltose = a glucose + a glucose
lactose = b glucose + galactose
sucrose = fructose + a glucose

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6
Q

describe the structure and function of starch

A

storage polymer of alpha glucose in plant cells
insoluble = no osmotic effect on cells
large = does not diffuse out of cells

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7
Q

what are the two types of starch

A

amylose
amylopectin

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8
Q

describe the structure and function of glycogen

A

main storage polymer of alpha glucose in animal cells
1,4 and 1,6 alpha glycosidic bonds
branched = many terminal ends for hydrolysis
insoluble = no osmotic effect and does not diffuse out of cells
compact

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9
Q

describe the structure and function of cellulose

A

polymer of beta glucose
gives rigidity to plant cell walls (prevents bursting under turgor pressure, holds stem up)
1,4 beta glycosidic bond
straight chain, unbranched molecule
alternate glucose molecules are rotated 180 degrees
H bonds crosslinks between parallel strands form microfibrils = high tensile strength
- cannot be stretched, stops the cell bursting

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10
Q

what is the difference between reducing and non-reducing sugars

A

reducing sugars can donate their electrons - the sugars become the reducing agent, thus reducing sugars can be detected using Benedict’s test as they reduce the soluble copper sulphate to insoluble brick-red copper oxide
non-reducing sugars cannot donate their electrons therefore they cannot be oxidised. it has to be hydrolysed first to break the disaccharides into its two monosaccharides before a Benedict’s test can be carried out.

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11
Q

what are some examples of reducing and non-reducing sugars

A

reducing - galactose, glucose and fructose
non-reducing - sucrose

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12
Q

what are 2 functions of glucose

A

as an energy source - it is the main substance used in respiration, releasing energy for the production of ATP
soluble and so can be transported in water

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13
Q

what are the 2 different forms of glucose

A

alpha (α) glucose and beta (β) glucose

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14
Q

what is an isomer

A

organic molecules with the same molecular formula but different structure which results in different properties
e.g. alpha (α) glucose and beta (β) glucose

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15
Q

what is the difference between ribose and deoxyribose

A

deoxyribose has lost one oxygen atom at carbon number 2

16
Q

what are the advantages of have monosaccharides bonded together

A

more suitable for transport
storage - more compact
cell osmolarity - polysaccharides and disaccharides have less -OH groups

17
Q

what are 3 common disaccharides

A

maltose: the sugar formed in the production and breakdown of starch
sucrose: the main sugar produced in plants
lactose: a sugar found in milk

18
Q

what are 3 examples of polysaccharides

A

starch
glycogen
cellulose

19
Q

amylose
1. name of bond
2. name of monosaccharide
3. shape + why

A

1,4 alpha glycosidic bond
alpha glucose
helix shape (twisted) caused by the hydrogen bonds between the -OH groups of the molecules

20
Q

amylopectin
1. name of monosaccharides
2. name of bond
3. structure

A

alpha glucose
1,4 alpha glycosidic and 1,6 alpha glycosidic bonds
branched (1,6 bonds create a branch)
branches can store lots of glucose molecules for when the body needs it
many terminals/ends of glucose units allows the rapid release / hydrolysis of glucose
make molecules compact so it can be stored in a small space

21
Q

what are the similarities of glycogen and amylopectin and what are the differences

A

glycogen has a similar structure to amylopectin but has more branches
glycogen is the animal storage molecule of alpha glucose and as animals, we have a higher metabolic rates and respire more and have a higher glucose requirement

22
Q

what are the 4 properties of a good storage molecule and what are the disadvantages

A

compact - not much volume by being coiled or branched
insoluble if they were soluble they would be able to dissolve in water instead of staying in the cell. due to condensation reaction, polysaccharides have less -OH groups
no osmotic effect - when polymerisation occurs, the glucose no longer attracts/pulls water into the cell due to less -OH groups
easy to hydrolyse/polymerise - lots of -OH groups that form H bonds

23
Q

amylopectin and glycogen have very similar structures and functions.
list the structural features shared by both amylopectin and glycogen and explain how they relate to their function

A

1,6 alpha glycosidic bond - branches - rapid release or digestion of glucose
lots of alpha 1,4 and 1,6 bonds - easy to polymerise / hydrolyse
insoluble + no osmotic effect - efficient
polysaccharides of alpha glucose - storage of alpha glucose