1.1. Amorphous solids - disordered structures (rubber, wax, glass) 1.2. Crystalline solids - particles arranged in a repeating pattern 1.2.1. Ionic solids - metal and nonmetal 1.2.1.1. Melting ionic compounds breaks ionic bonds 1.2.1.2. Lattice energy 1.2.1.2.1. Higher lattice energy with higher over ion charge, smaller ions, and higher melting point 1.2.1.3. Properties - high melting points, brittle, dissolves in polar solvents, conductor when melted/molten but not when solid or dissolved in water as they dissociate into free ions 1.2.2. Molecular solids - covalently bonded nonmetals 1.2.2.1. Held together by IMF’s 1.2.2.2. Properties - not conductible, relatively soft, low melting point 1.2.3. Atomic solids - atoms in a repeating pattern 1.2.3.1. Metallic solids - metal cations sharing delocalized valence electrons. Conductors, malleable, and ductile 1.2.3.1.1. Alloys 1.2.3.1.1.1. Substitutional alloys - similar atomic radius and density, malleable and ductile 1.2.3.1.1.2. Interstitial alloys - different atomic radii, smaller atoms fit in interstitial spaces of smaller atoms, rigid and strong but less malleable and ductile 1.2.3.1.1.3. Both are good conductors 1.2.3.2. Network solids - atoms with covalent bonds (usually group IV), hard, high density and high melting point (melting network solids breaks covalent bonds) 1.2.3.2.1. Carbon - many allotropes 1.2.3.2.1.1. Graphite - pressed into sheets, sheet held by covalent bonds, many sheets held together by IMF’s, high melting point and electric conductor 1.2.3.2.1.2. Diamond - hardest mineral, high durability, abrasive and high thermal conductivity 1.2.3.2.1.3. Fullerenes - stable, withstands high temperatures and pressures, investigated for use as a conductor (and nanotechnology) 1.2.3.2.2. Silicon - 3D network solid, strong, high melting point, semi conductor as electrical conductivity increases with increasing temp 1.2.3.2.3. Silica - silicon dioxide, found in sand and quartz, used for glass 1.3. Stronger bonding, higher melting/boiling points; ionic and metallic bonds are conductors; dipole dipole, hydrogen, and ionic bonds are soluble in water; there so much to knowwWW AAAAAAAAAAHHHHHHHHHHHHHHHHHH (p 9 notes) 2. Liquids - medium molecular motion and spacing 2.1. Higher IMF’s, higher surface tensions, viscosity, but lower vapour pressure (thus non-volatile, or less readily evaporatable 2.1.1. Pvapour =760 mmHg - PHg column 2.1.2. Vapour pressure increases with increases temperature (molecules move faster) 3. Gases - fast molecules and spaced very far apart 3.1. Kinetic energy 3.1.1. v= 1 √ 3RT M where M is mass of one mole of gas in kg/mol 3.1.2. 2 mv 2 = 32 RT 3.2. Diffusion - gas particles spread from high to low concentration r1 M2 3.3. Effusion - gas escapes from a hole in it’s container r2 = √ M1 where r is rate of a gas and M is molar mass 3.4. Gas collection over water - Pgas=Ptotal-Pwater from there use PV=nRT to solve for moles 3.5. Formation of gases in a reaction 3.5.1. Sulphide salt + acid = H2S and salt 3.5.2. Carbonate salt + acid = carbonic acid and salt which decomposes into carbon dioxide gas and water 3.5.3. Sulphite salt + acid = sulphurous acid and salt which decomposes into sulphur dioxide gas and water 3.5.4. Ammonium salt + base = ammonium hydroxide and salt which decomposes into ammonia gas and water 3.6. Real gases - ideal gas works when gases behave ideally. Gases not ideal when polar, at high pressures, or low temperatures. 4. Phase changes