Lipids. Flashcards
Gylcerol formula.
C3H8O3.
DIAGRAM.
Fatty acid tail formula.
At beginning, O=C-OH.
CH2 for each new tail.
CH3 at the end.
DIAGRAM.
Trigylceride properties.
One glycerol molecule.
Three molecules of fatty acids.
Fatty acid component can vary but glycerol always the same.
Formation of a triglyceride.
Fatty acids join to glycerol through a condensation reaction.
3 molecules of water are removed.
Ester bonds are formed between glycerol and fatty acids.
By product= 3H2O.
O-C=O is an ester bond.
3 reactions/3 ester bonds/3 water molecules for each triglyceride.
Lose hydrogen from glycerol and OH from the fatty acid= 3H2O.
Hydroxal from glycerol reacts with carboxyl group from fatty acid.
DIAGRAM.
Hydrolysis definition.
Water is chemically inserted in order to split up the H2O formed in the condensation reactions.
Saturated fatty acids.
- If the hydrocarbon chain has only single C-C bonds.
- All Carbon atoms are linked to the maximum possible numbers of Hydrogen atoms= saturated with hydrogen atoms.
- Chain= A straight zig-zag.
- Molecules can align easily so solid at room temp, more packing, strong attraction between fatty acid tails, regular pattern of CH2, fit readily.
- Found in animal lipids.
- Useful for storage in animnals.
DIAGRAM.
Unsaturated fatty acids.
- Carbon-Carbon bond is not a single bond.
- Mono= 1 double bond between Carbons.
- Poly= more than 1 double bond between Carbons.
DIAGRAMS. - Kink in the chain.
- Molecules cannot align uniformly/less packing/less attraction/irregular CH2 pattern so don’t solidify readily and usually liquid at room temp.
- Plant fats.
- Higher number of carbons= higher melting point.
What are steroid hormones made of?
Fats.
Uses of phospholipids.
- In biological membranes.
- Electrical insulation, myelin sheath surrounding axon on nerve cells.
Uses of triglycerides.
- Energy reserves in plants and animals (more C-H bonds than carbs so store more energy).
- Thermal insulation.
- Protection of delicate internal organs.
- Metabolic water (water released during chemical reactions in the body, lots produced by triglycerides when oxidised).
Uses of waxes.
- Waterproofing (reduce water loss in insect exoskeletons or cuticle of plants).
- Buoyancy (less dense than H2O).
Phospholipid structure.
2 fatty acid tails (hydrophobic), Glycerol, Phosphate group (PO4-).
Glycerol+Phosphate group=Phosphate/polar head.
DIAGRAM.
Properties of phosphate head.
Polar= hydrophilic= interacts with water= soluble in water.
Lots of O atoms= polar.
Fatty acid tails properties.
- Hydrophobic.
- Non-polar.
- Does not interact with water.
- No oxygen atoms= non-polar.
Glycerol properties.
Polar.
Hydrophilic.
Interacts with water/soluble.