Form triangle shape, hydrogen atoms are 104.5° from each other
Polar molecule
Due to unequal distribution of electron within the molecule<|>Oxygen atom is more electronegative than hydrogen atom<|>Shared electron of the covalent bond are closer at oxygen atom then hydrogen atom
Hydrogen bond
Attraction between δ+ H atom of one water molecule and δ- O atom of nearby water molecules<|>Weaker than covalent bonds but strong enough to hold water molecules
One water molecule can form maximum of 4 hydrogen bonds with 4 water molecules
In liquid state, water molecules continuously form, break and reform hydrogen bonds with each other
Universal solvent
Water's ability to dissolve many substances such as ionic compounds, other polar molecules and organic molecules
Specific heat capacity
Quantity of heat that must be absorbed or lost for 1g of substance to increase temperature by 1°C
Water has high specific heat capacity because a lot of energy is needed to increase the temperature of water to 1°C
Latent heat of vaporization
Quantity of heat must be absorbed for 1g of liquid to be converted to gaseous state
Water has high latent heat of vaporization because a lot of energy is absorbed to break the hydrogen bonds between water molecules to change from liquid to vapor
Cohesion of water molecules
Attractive forces between molecules of the same type (water)
Cohesive forces enable water molecules to stick together by hydrogen bond, producing high surface tension
Water has maximum density at 4°C
Above 4°C, water expands as it warms and contracts as it cools
At 0°C, water molecules form a crystalline lattice with each molecule hydrogen bonded to 4 other molecules
Ice is less dense than water because the hydrogen bonds in ice space the water molecules relatively far apart
The floating layer of ice insulates the water below, preventing them from losing heat and freezing
Classes of carbohydrates
Monosaccharide
Disaccharide
Polysaccharides
Formation and breakdown of maltose
1. Condensation reaction to form maltose
2. Hydrolysis reaction to break down maltose
α-glucose
Monomer of amylose, amylopectin and glycogen
Amylose
Monomers: α-glucose molecules
Joined together by α-1,4 glycosidic bond
Helical, unbranched chain (variable length of monomers)
Amylopectin
Monomers: α-glucose molecules
Joined together by α-1,4 glycosidic bond and α-1,6 glycosidic bond
Helical, branched chain (variable length of monomers)
Branches occur within 30 units
Folded & branched ~ very compact (ideal for storage)
Glycogen
Monomers: α-glucose molecules
Joined together by α-1,4 glycosidic bond and α-1,6 glycosidic bond
Helical, highly branched chain (variable length of monomers)
Structure is similar to amylopectin, but more branched
Cellulose
Monomers: β-glucose<|>Bonded by β-1,4 glycosidic bond<|>Unbranched, long straight chain
Cellulose
Major component of plant cell wall
Straight chains are arranged parallel to one another
Linked together by hydrogen bonds (form microfibril)
Very stable & tough structure ~ provide support to plant cell
Types of lipid
Triglycerides (fat & oil)
Phospholipids
Steroids
Lipids
Water insoluble organic molecules that contain C, H & O atoms<|>Soluble in organic solvent (alcohol, ether & chloroform)<|>Not true polymer- Not big enough to be considered macromolecules<|>Group of hydrophobic molecules ~ insoluble in water
Triglycerides
Consist of three fatty acids linked to one glycerol by ester linkage<|>Can be classified as saturated fat or unsaturated fat
Phospholipids
Major component of cell membrane<|>Amphipathic molecule, have both polar hydrophilic head and non-polar hydrophobic tails<|>Made up of glycerol, fatty acids and phosphate group
Steroids
Carbon skeleton consisting of 4 fused rings<|>No fatty acids
Glycerol
3C alcohol with 3 hydroxyl groups (-OH) attached
Fatty acids
Have a carboxyl group (-COOH) at one end and a hydrocarbon chain (R) at the other end<|>Can be classified as saturated or unsaturated
Formation of triglycerides
1. 3 condensation/esterification reactions between 3 fatty acids and 1 glycerol
2. Removal of 3 water molecules
Breakdown of triglycerides
1. 3 hydrolysis reactions to break the 3 ester linkages
2. Addition of 3 water molecules
Amino acids
Building blocks/monomers of proteins<|>Have a central carbon atom, amino group (-NH2), carboxyl group (-COOH) and a side chain (R group)