first ionisation energy = enthalpy change when each atom in one mole of gaseous atoms loses one electron to form one mole of gaseous 1+ ions
second ionisation energy = enthalpy change when each ion in one mole of gaseous 1+ ions loses one electron to form one mole of gaseous2+ions
Endothermic
eg 1. Mg(g) -> Mg+(g) + e-
eg 2. Mg+(g) -> Mg2+(g) +e-
Electron affinity ΔeaH⦵
First electron affinity= enthalpy change when each atom in one mole of gaseous atoms gainsoneelectron to form one mole of gaseous 1- ions (exothermic)
Second electron affinity= enthalpy change when each ion in one mole of gaseous 1- ions gainsoneelectron to form one mole of gaseous 2- ions (endothermic)
eg 1. O(g) + e- -> O-
eg 2. O-(g) + e- -> O-2
Enthalpy of atomisation ΔatH⦵
Enthalpy change when onemole of gaseous atoms is produced from an element in its standard state
Endothermic
1/2I2(s) -> I(g)
Hydration enthalpy ΔhydH⦵
enthalpy change when one mole of gaseous ions become hydrated
Exothermic
eg. Mg2+(g) + aq -> Mg2+(aq)
Enthalpy of solution ΔsolH⦵
Enthalpy change when one mole of an ionic solid dissolves in an amount of water large enough so that the dissolved ions are well separated and do not interact with each other
Exo/Endo varies
eg. MgCl2(s) + aq -> Mg2+(aq) + 2cl-(aq)
Bond dissociation enthalpy ΔdisH⦵
Enthalpy change when one mole of covalent bonds is broken in the gaseous state
Endothermic
eg. I2(g) -> 2I(g)
Lattice enthalpy of formation ΔlefH⦵
enthalpy change when one mole of a solidioniccompound is formed into its constituentions in the gas phase
exothermic
eg. Mg2+(g) + 2Cl-(g) -> MgCl2(s)
lattice enthalpy of dissociation ΔledH⦵
Enthalpy change when one mole of a solid ionic compound is broken up into its constituent ions in the gas phase
endothermic
eg. MgCl2(s) -> Mg2+(g) + 2Cl-(g)
Enthalpy of vaporisation ΔvapH⦵
Enthalpy change when one mole of a liquid is turned into a gas
Endothermic
eg. H2O(l) -> H2O(g)
Enthalpy of fusion ΔfusH⦵
enthalpy change when one mole of a solid is turned into a liquid