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Define monomer
Smaller, repeating units from which larger molecules/polymers are made.
Define Polymer
Molecules made from many identical/similar monomer molecules.
What 3 things happen in a condensation reaction?
2 molecules join together
forming a chemical bond
releasing a water molecule
What 3 things happen in a hydrolysis reaction?
2 molecules seperated
breaking a chemical bond
Using a water molecule
Nucleotide is a monomer. What is its polymer?
Polynucleotide (DNA or RNA)
What is the polymer of glucose?
starch
What is the polymer of amino acids?
proteins
What are monosaccharides?
monomers from which large carbohydrates are made.
Give 3 examples of monosaccharides
Glucose
fructose
galactose
Draw structure of a-glucose
OH on bottom of both sides
Describe the difference between the structure of a-glucose and B-glucose
Isomers - same molecular formula but differently arranged atoms
OH group is below carbon 1 in a-glucose but above carbon 1 in B-glucose
What are disaccharides and how are they formed?
2 monosaccharides joined together with a glycosidic bond.
Formed by a condensation reaction, releasing a water molecule
List 3 common disaccharides and monosaccharides from which they’re made.
a-glucose + a-glucose = maltose
glucose + galactose = lactose
fructose + glucose = sucrose
What are polysaccharides and how are they formed?
many monosaccharides joined together with glycosidic bonds
Formed by many condensation reactions, releasing many water molecules
What’s the basic function of starch?
Energy store in plant cells
What’s the basic function of glycogen?
Energy store in animal cells
State 3 points regarding the basic structure of starch
Polysaccharide of a-glucose
Some has 1,4-glycosidic bonds so is unbranched (amylose)
some has 1,4- and 1,6-glycosidic bonds so is branched (amylopectin)
State 2 points regarding the basic structure of glycogen
polysaccharide made of a-glucose
1,4- and 1,6-glycosidic bonds = branched
Explain how the structure of starch (amylose) relates to its function.
Helical - compact for storage in cell
Large, insoluble polysaccharide molecule - can’t leave cell/cross cell membrane
Insoluble in water - water potential of cell not affected (no osmotic effect)
Explain how the structures of glycogen and starch amylopectin relate to their functions
branched = compact
branched = more ends for faster hydrolysis - release glucose for respiration to make ATP for energy release
Large, insoluble polysaccharide molecule - can’t leave cell/cross cell membrane
insoluble in water - water potential of cell not affected (no osmotic effect)
Describe the basic function of cellulose
Provides strength and structural support to plant/algal cell walls
Describe the basic structure of cellulose
Polysaccharide of B-glucose
1,4-glycosidic bonds so forms straight, unbranched chains
Chains linked in parallel by hydrogen bonds, forming microfibrils
Explain how the structure of cellulose relates to its function
Every other B-glucose molecule is inverted in a long, straight, unbranched chain.
Many hydrogen bonds link parallel strands to form microfibrils (strong fibres).
Hydrogen bonds are strong in high numbers
so provides strength to plant cell walls
Name 3 reducing sugars
monosaccharides, maltose and lactose
Describe the test for reducing sugars in 3 steps
Add Benedict’s solution (blue) to sample
Heat in a boiling water bath
Positive result = green/yellow/orange/brick red precipitate
Describe the test for non-reducing sugars in 5 steps
Do Benedict’s test and stays blue/negative
heat in a boiling water bath with acid (to hydrolyse into reducing sugars)
neutralise with alkali (e.g. sodium bicarbonate)
heat in a boiling water bath with benedict’s solution
positive result = green/yellow/orange/brick red precipitate
Name a non-reducing sugar
sucrose
Suggest a method to measure the quantity of sugar in a solution
Carry out Benedict’s test, then filter and dry precipitate
find mass/weight
Describe the biochemical test for starch
Add iodine dissolved in potassium iodide (orange/brown) and shake/stir
Positive result = blue-black
Name 2 groups of lipid
triglycerides and phospholipids