Enthalpy and Entropy Word Stimulants Flashcards
Lattice Enthalpy
Measure of ionic strength in giant ionic lattice
Exothermic (formation of bonds) H -
Lattice Enthalpy* Definition
Enthalpy change that accompanies the formation of one mole of an ionic compound from its gaseous ions under standard conditions.
Born - Harber Cycle
Left: Formation (down arrow) ; elements standard states; Atomisation ^; gaseous atoms; first ionisation energy ^
Right: Electron affinity (down arrow); gasous ions; lattice enthalpy change (down arrow)
Bottom : ionic lattice
Enthalpy Change of Formation*
Enthalpy change for the formation of 1 mol of a compound from its elements in their standard states under standard conditions.
Enthalpy change of atomisation
Formation of 1 mol of gaseous atoms from the electrons in SS under SC.
First ionisation energy*
Enthalpy change for the removal of 1 e- from each arom in 1 mol of gaseous atoms to form 1 mol of gaseous 1+ ions.
First electron affinity
Addition of 1 e- to each atom in 1 mol of gaseous atoms to form 1- ions.
Enthalpy change in solution
Dissolve ionic compound in H2O
Ionic lattic breaks up -> gaseous ions -> bond to h2o -> aq ions
Lattice enthalpy in solution
Energy to break ionic bonds
Formation : endothermic
Breaking : exothermic
Enthalpy Change of hydration
Enthalpy change when one mole of gaseous ions dissolve in water to form aqueous ions
g + aq -> aq
Exothermic
Enthalpy change of solution
Enthalpy change when one mole of a solute dissolves in a solvent
Exothermic or endothermic
Born-Harber Soltution
Top: Gaseous ions
Bottom: Ionic Lattice
Left : Lattice Enthalpy
Right: Hydration (down arrows); aq ions; Solution ^ (at bottom)
Factors affecting lattice enthalpy
Ionic size
ionic charge
Ionic size increase
Attraction between oppositiely charge ions decrease - ionic radius +
Lattice enthalpy change - less exothermic
Melting point decrease - less energy to overcome decreased attraction
Ionic charge increase
Attraction between oppositiely charge ions increase
Lattice enthalpy change - more exothermic
Melting point increased - more energy to overcome increased attraction
Factors affecting Hydration enthalpy
Ionic size
Ionic charge
Ionic size decrease, ionic charge increase
Attraction between ions and h20 +
Enthalpy change of hydration more exothermic
Entropy
S
Measure of the dispersal of energy in a system
Greater Entropy
Greater dispersal, greater disorder
More positive
Standard Entropy Change
Entropy content of 1 mol of a substance under standard conditions
KJ-1mol-1
Always positive
Solid > Liquid > Gas
Particals more random
S increases , more +
Gaseous moles
Increase in gaseous molecules = increase entropy
Decrease in gaseous molecules = decrease entropy
S calculation
(Sum of) S products - (Sum of) S reactants
Free Energy Change
G
Overall energy change of reaction
Feasible
Products lower energy than reactants
G<0 (negative G)
H-TS<0
G Calculation
G = H - TS (kJmol-1) Enthalpy change (kJ mol-1) Temp (K) Entropy change of system (JK-1mol-1) divide by 1000
Temperature increase effect on G
TS more significant
May outweigh H
Not feasible
Limitations of free energy
G not take into account rate (slow)