7.2. Energetics 2 Flashcards

1
Q

enthalpy change of a reaction =

A

enthalpy of formation (products) - enthalpy of formation (reactants)

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2
Q

is there a change is enthalpy if only the intermolecular bonds are broken?

A

yes, the enthalpy of formation is different for different states of the same compound

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3
Q

Born-Haber cycle equation

A

enthalpy of formation = enthalpy of sublimation + first ionization enthalpy + first electron affinity + enthalpy of disssociation + lattice energy (MX example)

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4
Q

standard enthalpy change of atomisation

A

the enthalpy change when one mole of atoms in a gasous state is formed from the element in its standard state
- (delta)Hat

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5
Q

first electron affinity

A

the enthalpy change when one mole of gaseous atoms each gain one electron
- (delta)HEa

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6
Q

first ionization enthalpy

A

the enthalpy change when one mole of gaseous 1+ ions are formed from one mole of gaseous atoms
- (delta)Hi(1)

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7
Q

lattice enthalpy

A

the enthalpy change when one mole of solid ionic compound is made from gaseous ions - it increases with the charge of ions and increases with the decreasing size of ions
- (delta)HLE

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8
Q

the greater the charges of ions,…

A

the greater the E holding them together (lattice E)

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9
Q

spontaneous reactions/processes

A
  • generally exothermic
  • the final state is more disordered/random than the original => (delta)S>0
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10
Q

spontaneity is related to ___, and the thermodynamic property related to ___ is…

A

an increase in randomness,
randomness,
entropy (S) [J/Kmol)

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11
Q

entropy increases with:

A

1) state (g>l>s)
2) temperature (less than state)
3) molecular complexity
4) depending on coulombic attractions

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12
Q

(delta)S=

A

S(products) - S(reactants)

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13
Q

when is a reaction spontaneous (relating to (delta)H and (delta)S?
(table)

A

H<0, S>0 - spontaneous
H<0, S<0/H>0, S>0 - depends on magnitudes (more favorable in lower T/more favorable in higher T)
H>0, S<0 - not spontaneous

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14
Q

(delta)S<0/>0 meaning

A

<0 = more order
>0 = less order (characteristic of spontaneous reactions)

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15
Q

-(delta)H (system) is proportional to…
*

A

(delta)S (surroundings) - an exothermic process has (delta)S (surroundings)>0

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16
Q

Gibbs free E change =

A

total E change for the system ((delta)H (system)) - E lost in disordering the system (T*(delta9S (system))

17
Q

when is a reaction P and when R-favored (relating to Gibbs free E change, (delta)H and (delta)S)?
(table)

A

1) H<0, S>0 => G<0 (P-favored, spontaneous)
2) H>0, S<0 => G>0 (R-favored, not spontaneous)
3) H, S<0 / H, S>0 - depends on T values (spontaneous at low T(spontaneous at high T)

18
Q

Gibbs free E change for an element is…

A

zero

19
Q

(delta)G>/<0 meaning
*

A

(delta)G<0 => spontaneous, enthalpy driven
(delta)G>0 => not spontaneous, entropy driven

20
Q

(delta)G (reaction) =

A

(delta)G (products) - (delta)G (reactants)