Polar molecule due to uneven distribution of charge; oxygen is more electronegative than hydrogen. Makes water a good solvent; it can form electrostatic interactions with other polar molecules and ions.
Water in reactions
Can act as a metabolite in reactions such as condensation and hydrolysis. Can act as a buffer because of its high SHC; minimises its temperature fluctuations.
Water's density
Maximum density of water is 4*C
Density of ice vs. density of water
Ice is less dense than water so can float on top; creates an insulating layer preventing animals living in water from freezing - water can act as a habitat.
Water and Latent Heat of Vaporisation
Has a high Latent Heat of Vaporisation; strong hydrogen bonds which gives the evaporation of water provides a cooling effect through sweating (little H2O is lost) and prevents dehydration in transpiration.
Incompressible
Water in incompressible; provide good support. For example a hydrostatic skeleton for small animals and gives turgidity to plant cells.
Cohesion of Water
Strong hydrogen bonds give water strong cohesive forces and hence, high tensile strength. Strong cohesion is good for supporting columns of water; high surface tension slows water loss through transpiration.
Cohesion
Refers to the attraction of one water molecule to another.
Condensation Reaction
Forms bonds; water is produced.
Hydrolysis Reactions
Breaks bonds; water is added to break bonds.
Monomer
Smaller units that join together to form large molecules (e.g. monosaccharides, amino acids, nucleotides)
Polymer
Molecules formed when many monomers joing together, e.g. polysaccharides, proteins, DNA/RNA.
Macromolecules
Large and complex molecules that are formed due to the polymerisation of smaller monomers.
Carbohydrates
Contain the elements C,H,O. Have three types; mono, di, and polysaccharides.
Monosaccharides
Simplest carbohydrate, can't be hydrolysed.
Glucose
Glucose is a monosaccharide and is the main substrate for respiration. Has two isomers.
Disaccharides
Two monosaccharides joined by a glycosidic bond.
maltose —> two glucose molecules
sucrose —> glucose + fructose
lactose —> glucose + galactose
Alpha Glucose vs Beta Glucose
Hydroxyl (OH) is on the bottom in alpha glucose, at the top in beta glucose.
Glycosidic bonds
Covalent bond formed due to a condensation reaction to make di and polysaccharides.
Polysaccharides
Formed from many glucose units joined togther
Glycogen
Formed from the condensation of alpha glucose; joined together by 1,4 and 1,6 glycosidic bonds.
Properties of glycogen
Branched; easily hydrolysed so glucose (hence energy) can be released quickly. Large but compact; maximises energy it can store. Insoluble; doesn't affect water potential and doesn't diffuse out of cells.
Starch
Mixture of two polysaccharides; amylopectin and amylose. Highly compact and stores energy.
Amylose
Unbranched, 1-4 glycosidic bonds, coiled, very compact (stores lots of energy).
Amylopectin
Branched, 1-4 and 1-6 glycosidic bonds, branches for rapid digestion by enzymes to release energy quickly.
Cellulose
Polymer of beta glucose that gives rigidity to plant cell walls. Has 1-4 glycosidic bonds in a unbranched, straight chain; alternate beta glucose molecules are rotated 180* to form these bonds. Hydrogen bonds form between parallel molecules to form microfibrils (high tensile strength) - helps them withstand osmotic pressure, and are freely permeable.
NO3-
Used in DNA, amino acids, NADP (photosynthesis), NAD (respiration)
NH4+
Can be converted to NO3- during the nitrogen cycle. Produced by the deamination of amino acids in the liver.
OH-
Affects pH and interacts with bonds in proteins to cause denaturation.
(PO4)3-
Component of ATP/ADP for energy release, and NADP.
Na+ and K+
Generates nerve impulses. Na+ is involved in co-transport mechanisms.
Cl-
Keeps the pH of the blood constant in gas exchange.
Form from a condensation reaction between a glycerol and three fatty acid chains, forming an ester bond. Broken down by hydrolysis. Only soluble in organic solvents, e.g. alcohols.
Saturated Triglycerides
Contain only single bonds; straight chain molecules with many contact points. Have higher melting points (solid at room temperature), found in animal fats.
Unsaturated Trigylcerides
Contain C=C double bonds, causing kinks. Hence, less points of contact, lower melting points (weaker IMF's) so are liquid at room temperature. Found in plant oils.
Formation of Triglycerides
Glycerol undergoes condensation reaction with three fatty acid chains, forming triglyceride and a bi-product of 3H2O.