4.4 Entropy and Gibbs free energy Flashcards

1
Q

what can be exchanged in an OPEN SYSTEM

A

energy and matter

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2
Q

what can be exchanged in a CLOSED SYSTEM

A

energy only

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3
Q

what can be exchanged in an ISOLATED SYSTEM

A

neither energy nor matter

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4
Q

entropy is a measure of…

A

possible arrangements with the same overall energy

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5
Q

entropy change equation

A

∆S = S(products) − S(reactants)

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6
Q

2nd law of thermodynamics

A

entropy of the universe is always increasing

∆S(system) + ∆S(surroundings) = ∆S(universe) > 0

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7
Q

increasing temperature…

A

increases kinetic energy > increases possible arrangements > increases entropy

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8
Q

increasing concentration…

A

increases possible arrangements > increases entropy

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9
Q

why entropy of liquid > solid

A

non-fixed vs fixed structure

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10
Q

why entropy of gas > liquid

A

continual movement and occupying more volume

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11
Q

what is solid dissolution and why does it increase entropy

A

a solid solute dissolves in a solvent to form an aqueous solution

solute particles have more possible arrangements

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12
Q

spontaneous reaction

A

any natural reaction that doesn’t need external energy

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13
Q

3rd law of thermodynamics

A

the THEORETICAL entropy of a perfect crystal (lattice) is zero

only 1 arrangement; no vibration; no kinetic energy

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14
Q

standard enthalpy

A

standard conditions 25C and 1 bar pressure

∆Sdeg = ΣSdeg(products) - ΣSdeg(reactants)

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15
Q

Gibbs free energy equation and all units involved

A

∆G = ∆H - T∆S

∆G in kJ/mol
∆H in kJ/mol
T in Kelvins (careful)
∆S in J K-1 mol-1 (careful)

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16
Q

∆G < 0, ∆G > 0
and ∆G = 0

A

if ∆G = neg, it’s spontaneous
if ∆G = pos, it’s not spontaneous

if ∆G = 0, the reaction is at equilibrium (module 5)

17
Q

reaction is spontaneous at all T when:

A

∆H < 0 (neg)
T∆S > 0 (pos)

18
Q

reaction is NOT spontaneous at any T when:

A

∆H > 0 (pos)
T∆S < 0 (neg)

19
Q

if ∆H = pos,
reaction is spontaneous at HIGH T when:

A

∆H < T∆S
so ∆H - T∆S < 0 if T is large

20
Q

if ∆H = neg,
reaction is spontaneous at LOW T when:

A

∆H > T∆S
so ∆H - T∆S < 0 if T is small