Physical Chemistry 2 Flashcards

1
Q

Thermodynamics- Enthalpy Change of Formation

A
  • enthalpy change when one mole substance formed from constituent elements under standard conditions, standard states
  • Na(s) + 1/2Br2(l) -> NaBr(s)
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2
Q

Thermodynamics- Born-Haber Cycles

A
  • Method:
    Enthalpy of formation AB -
    Atomisation of A +
    Atomisation of B +
    Ionisation energy A +
    Electron affinity B -
    Lattice formation enthalpy AB -
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3
Q

Thermodynamics- Enthalpy of Solution

A
  • Enthalpy change of solution=Enthalpy change when one mole of substance completely dissolved in water
  • Made of two steps:
    Lattice dissociation enthalpy (endo)
    Hydration enthalpy (exo)
  • Hydration enthalpy=enthalpy change when one mole gaseous ions completely dissolved in water
  • Factors affecting size of hydration enthalpy:
    Smaller ion=stronger attraction
    More highly charged an ion=stronger attraction
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4
Q

Thermodynamics- Perfect Ionic Model

A
  • Theoretical value:
    Fully ionic (no covalent character)
    All ions are point charges
  • Experimental value:
    Born-Haber cycles- standard enthalpy changes
    Hess cycles
  • Shared electrons add covalent character
  • Theoretical and experimental similar (no covalent character):
    High difference in electronegativity
    Relatively small anion(negative)
  • Theoretical and experimental different (add covalent character):
    Small difference in electronegativity
    Large anions(negative)
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5
Q

Thermodynamics- Entropy Change

A
  • Entropy=a numerical measure of disorder in a chemical system
  • Factors affecting entropy:
    High temp=high entropy
    Arrangement in space
    Highly ordered (solid)=low entropy
    Highly disordered (gas)=high entropy
  • Entropy(ΔS)=products - reactants
  • Gibb’s free energy:
    ΔG=ΔH-TΔS
  • When ΔG=0, this is the point at which the reaction is feasible (reaction takes place of its own accord)
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6
Q

Equilibrium Constant Kp- Homogenous Systems

A
  • Partial pressure=the pressure the gas would exert if it occupied a container on its own
  • Total pressure=sum of partial pressures of all the gases in a mixture
  • Partial pressure of A=mole fraction of A x total pressure
  • Mole fraction of gas A=number of moles of gas A in mixture / total number of moles of gas in mixture
  • Kp=products / reactants
  • Effect of changing temp and pressure on gaseous equilibrium:
    Increase temperature=decrease Kp=decrease yield
    Increase pressure=increase Kp=increase yield
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7
Q

Thermodynamics- Enthalpy Change of Combustion

A
  • enthalpy change when one mole of substance completely burned in oxygen under standard conditions, standard states
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8
Q

Thermodynamics- Enthalpy Change of Atomisation

A
  • enthalpy change when one mole of gaseous atoms is formed from an element under standard conditions in standard states
  • 1/2 O2(g) -> O(g)
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9
Q

Thermodynamics- First Ionisation Energy

A
  • standard enthalpy change when one mole gaseous atoms converted into one mole of positive gaseous ions
  • Mg(g) -> Mg+(g) + e-
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10
Q

Thermodynamics- First Electron Affinity

A
  • standard enthalpy change when one mole gaseous atoms converted into one mole of negative gaseous ions
  • O2(g) + e- -> O2-(g)
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11
Q

Thermodynamics- Lattice Enthalpy of Formation

A
  • standard enthalpy change when one mole solid ionic compound formed from constituent elements
  • Na+(g) + Br-(g) -> NaBr(s)
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12
Q

Thermodynamics- Lattice Enthalpy of Dissociation

A
  • standard enthalpy change one mole solid ionic compound dissociates into gaseous ions
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13
Q

Thermodynamics- Enthalpy of Hydration

A
  • standard enthalpy change one mole gaseous ions converted into aqueous ions
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14
Q

Thermodynamics- Enthalpy of Solution

A
  • standard enthalpy change when one mole solute dissolves completely in sufficient solvent to form solution where ions won’t interact with each other
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15
Q

Thermodynamics- Mean Bond Enthalpy

A
  • enthalpy change when one mole gaseous molecules breaks covalent bond to form two free-radicals, averaged over range of compounds
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