Chapter 22: enthalpy and entropy (22.1 - 22.3) Flashcards

1
Q

what does lattice enthalpy measure

A

the strength of the ionic bonding in a giant ionic lattice

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2
Q

define lattice enthalpy (Δlatt H)

A

the enthalpy change the accompanies the formation of 1 mole of an ionic compounds from its gaseous ions under standard conditions.
It is always exothermic

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3
Q

how do you work out lattice enthalpy (not experimentally)

A

born-haber cycles (see page 346 in textbook)

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4
Q

define standard enthalpy of formation (Δf H)

A

the enthalpy change that takes place for the formation of one mole of gaseous atoms from the elements in their standard states under standard conditions

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5
Q

define standard enthalpy of atomization (Δatt H)

A

the enthalpy change that takes place for the formation of 1 mole of gaseous atoms from the element in its standard state under standard conditions

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6
Q

define first ionization energy (ΔIE1 H)

A

the enthalpy change required to remove 1 electron from each atom in 1 mole of gaseous atoms to form 1 mole of gaseous 1+ ions.

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7
Q

define first/second electron affinity (ΔEA1 H / ΔEA2 H)

A

Energy required for each atom/ion in 1 mole of gaseous atoms/1- ions to gain 1 electron to form 1 mole of gaseous 1- ions/2- ions

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8
Q

difference between first and second electron affinity

A

EA1 is exothermic (-ΔH)

EA2 is endothermic (+ΔH)

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9
Q

factors affecting lattice enthalpy

A

ionic radius: smaller ions = stronger attraction = larger lattice enthalpy

ionic charge: larger charge = stronger attraction = larger lattice enthalpy

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10
Q

define enthalpy change of solution (Δsol H)

A

the enthalpy change that takes place when 1 mole of solute is dissolved in a solvent.
If the solvent is water, the ions from the ionic lattice are surrounded with water molecules as aqueous ions.
Can be endothermic or exothermic.

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11
Q

what happens when an ionic compound dissolves

A
  • ionic lattice eurekas up forming gaseous ions (opposite of Δlatt H)
  • water molecules are attached to, and surround the ions. Gaseous ions interact w polar water molecules to from hydrated aqueous ions (Δhyd H)
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12
Q

how does water attach to the ions which are being dissolved

A

𝛿- oxygen attracted to positive ion

𝛿+ hydrogen attracted to negative ion

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13
Q

equation to work out energy change

A

q = mcΔT

q joules, m grams, c given, ΔT in K (change in temp)

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14
Q

define enthalpy change of hydration (Δhyd H)

A

the enthalpy change that accompanies the dissolving of gaseous ions in water forming 1 mole of aqueous ions

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15
Q

general properties of ionic compounds

A

high melting and boiling points
soluble in polar solvents
conduct electricity when molten or in aqueous solution

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16
Q

factors effecting hydration

A

ionic radius: smaller ions = stronger attraction between ion and water molecule = hydrations energy more negative

ionic charge: larger charge = stronger attraction = more negative hydration energy

17
Q

what is entropy

A

a measure of the dispersal of energy in a system

units: J/K/mol

18
Q

greater the entropy means

A

greater disorder / greater dispersal of energy
eg. solid -> liquid is increase in entropy
1 mol gas -> 2 mol gas is increase in entropy

19
Q

why do reactions tend towards higher entropy

A

energy has a natural tendency to spread out rather than be concentrated in one place

20
Q

equation for entropy change ΔS°

A

ΔS° = ΣS°(products) - ΣS°(reactants)

21
Q

what is feasibility

A

feasibility describes weather a process can take place. A reaction is ‘energetically feasible’ if the free energy change (ΔG) is negative

22
Q

equation for free energy ΔG

A

ΔG = ΔH - TΔS
(ΔH= enthalpy change of reaction. K= temp in K. ΔS= entropy change of reaction)
remember to convert ΔS into kJ as its standardly in J

23
Q

units of ΔG

A

kJ/mol

24
Q

limitations on ΔG for determining if a reaction will happen

A
  • takes no account of the kinetics (rate of reaction, activation energy)
  • assumes standard conditions