Topic 15: Energetics and Themochemistry (HL) Flashcards
Born-Haber cycle
A series of reactions that can be combines to determine the enthalpy of formation of an ionic compound
Constructing a Born-Haber cycle
Step 1: Lattice enthalpy
MX (s) → M^(+)(g) + X^(-)(g) ∆Hlat > 0
Process is endothermic
Step 2: Enthalpy of atomization
M(s) → M(g) ΔHat>0
1/2X2(g) → X(g) ΔHat>0
Step 3: Ionization energy
IE1: M(g) → M+(g) +e ∆HIE>0
IE2: M+(g) → M2+(g) + e ∆HIE2>0
Step 4: Electron affinity
X(g) + e → X (g) ∆HEA<0
Lattice enthalpy
The standard enthalpy change that occurs on the formation of 1 mol of gaseous ions from the solid lattice
MX (s) → M^(+)(g) + X^(-)(g) ∆Hlat > 0
Directly affected by both the charge on the ions and the atomic radii, ie. an increase in ionic charge equals greater attraction between oppositely charged ions, increasing the energy required to break apart the ionic lattice.
As the ionic radii increases, the electrostatic attraction decreases, ie decrease in lattice enthalpy
Enthalpy of atomization
The standard enthalpy change
that occurs on the formation of 1 mol of separate gaseous atoms of an element in its standard state
M(s) → M(g) ΔHat>0
1/2X2(g) → X(g) ΔHat>0
Electron affinity
The standard enthalpy change
on the addition of 1 mol of electrons to 1 mol of atoms in the gaseous phase
Standard enthalpy change of solution
The change in
enthalpy when 1 mol of a substance is dissolved in a large excess of a pure solvent
Enthalpy change of hydration
For an ion is the enthalpy
change when 1 mol of the gaseous ion is added to water to form a dilute solution.
Always has a negative value
M+(g) → M+(aq) ∆Hhyd= - kJ mol 1
X (g) → X (aq)
∆Hhyd= - kJ mol 1
Solvation
term used in place of hydration for solvents other than water
Spontaneous reaction
When a reaction moves towards either completion or equilibrium under a given set of conditions without external intervention.
Occur at different rates.
Either endothermic or exothermic
Lead to an increase in the total entropy within the system and surroundings.
Entropy, S
A measure of the distribution of total available energy between the particles.
The greater the shift from energy being localized to being widespread amongst the particles, the lower the chance of the particles returning to their original state and the higher the entropy of the system.
Increase in entropy as the particles gain more freedom of movement, ie solid to liquid to gas.
How to determine entropy?
It’s a state function, so a change in entropy is determined by the difference between its final and initial values:
∆ S 298(reaction) = ∑∆ S 298 (products) - ∑∆ S 298 (reactants)
Second law of thermodynamics
Chemical reactions that result in an overall increase in the entropy of the universe are spontaneous.
When the overall entropy of the universe remains unchanged, the system is in equilibrium.
∆Stotal = ∆Ssystem + ∆Ssurroundings
∆Stotal > 0
spontaneous
∆Stotal = 0
equilibrium
∆Stotal < 0
non-spontaneous