Topic 12 Flashcards
Entropy
disorderliness of the system
more molecules / phase of the substance can increase the entropy
ΔS(system)
change of state / change of number of molecules between solid and gases
ΔS(system) = ∑S(products) - ∑S(reactants)
ΔS(surrounding)
ΔS(surrounding) = -ΔH/T
exothermic –> energy given out into surroundings, more ways arranging energy –> increase entropy
endothermic –> energy transferred from surroundings, number of ways to arrange energy decreased –> decrease entropy
ΔS(total)
ΔS(total)=ΔS(surrounding)+ΔS(system)
positive ΔS(total) –> reaction is THERMODYNAMICALLY stable and is spontaneous
Enthalpy change of formation
The energy required to form a mole of the compound from its elements under standard conditions. (at elements normal state)
Enthalpy of atomisation
Enthalpy change when a mole of gaseous atom is formed from the element in its standard state.
Na(s) –> Na(g)
1/2 O2(g) –> O(g)
First ionisation enthalpy
Enthalpy change required to remove a mole of electrons from a mole of gaseous atoms to form a mole of gaseous ion with a +1 charge
Second ionisation enthalpy
Enthalpy change required to remove a mole of electrons from a mole of gaseous ion with +1 charge to form a mole of gaseous ion with a +2 charge
First electron affinity
Enthalpy change that is required when a mole of gaseous atoms gain a mole of electrons to form a mole of gaseous ions with -1 charge
Secondary electron affinity
Enthalpy change that is required when a mole of gaseous -1 ion gains a mole of electron to form a gaseous ion with -2 charge
(endothermic as it requires energy to overcome the repulsive force between -1 ion and the electron)
Enthalpy of lattice formation
Enthalpy change when a mole of an ionic crystal lattice is formed from its constituent ion in gaseous form.
How does size of ions and charges of ion affect the enthalpy of lattice formation
Larger ions, less negative the enthalpies of lattice formation as the ions are larger the charges become further apart and so have a weaker attractive force between them
Bigger the charge of ion, greater the attraction between the ions so stronger the lattice enthalpy (more negative value)
Born Haber Cycle
remember to add electron for ionisation energy
if need 2 like MgCl2 , when doing atomisation and electron affinity need to times 2
if one like NaCl, but Cl2 is standard state, need to write 1/2 Cl2
Perfect ionic model
ions are 100% ionic and spherical and attractions are purely electrostatic
Theoretical value vs Experimental lattice enthalpies
Because have covalent character due to polarisation. Negative ion becomes distorted and more covalent –> polarised by the positive ion.
Polarising power of cation
Increases when positive ion is small and has larger charge = larger charge density –> polarise anion better
Enthalpy of hydration
Enthalpy change when a mole of gaseous ions becomes hydrated such that further dilute causes no further heat change
Enthalpy of solution
Enthalpy change when a mole of an ionic solid dissolves in a large enough amount of water
Calculation to determine enthalpy change of solution
Δsol. H = -ΔLE H + ∑Δhyd H
Δsol. H: MgCl2(s) + aq –> Mg2+(aq) + 2Cl- (aq)
ΔLE H: Mg2+(g) + 2Cl- (g) –> MgCl2 (s)
Δhyd H: Mg2+ (g) + aq –> Mg2+ (aq)
Why some ionic solids are soluble and some are not
Δsol.H is exothermic to be soluble
Δsol.H is endothermic to be insoluble