Lecture 17- Thermodynamics 3 Flashcards

1
Q

Thermodynamically favored process

A
  • spontaneous
  • proceeds without any assistance from outside the system
  • Ex. Water evaporates at 25C, iron rusts with O2 and H2O
  • NaCl dissolves in water
  • A process that is thermodynamically favored in one direction is non-thermodynamically favored in the other direction
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2
Q

TFP exothermic

A
  • exothermic reactions are often thermodynamically favored
  • nature tends to favor processes that cause a reduction in energy
  • In an exothermic reaction, the bonds in the products contain less energy than the bonds in the reactants. The excess energy is released as heat.
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3
Q

TFP endothermic

A
  • endothermic reactions can be thermodynamically favored
  • evaporation is thermodynamically favored
  • dissolving soluble compounds is thermodynamically favored
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4
Q

entropy

A
  • a measure of the disorder of a system
  • a greater degree is favorable
  • a positive value for ^S is favorable
    ^S=S(products)-S(reactants)
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5
Q

laws of thermodynamics

A
  1. The energy contained within the universe is constant

2. The entropy of the universe is constantly increasing

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6
Q

S>0

A
  • melting
  • vaporization
  • reactions where the products are in the same phase as the reactants but contain more particles than the reactants
  • making most solutions
  • adding heat
  • increasing volume of gas
  • when products have more particles
  • volume increases
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7
Q

calculating ^S

A

^S=sum n S(products) - sum n S(reactants)

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8
Q

How to tell if a process is thermodynamically favored

A
  • exothermic reactions are favored so ^H0
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9
Q

Two methods for determining if a process is thermodynamically favored

A
  1. ^S(universe)- theoretical

2. ^G (Gibbs free energy)

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10
Q

^S universe

A

^S (universe)=^S (system) + ^S (surroundings)

- If ^S>0, the reaction is thermodynamically favored, its its negative then it won’t happen at all

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11
Q

Gibbs free energy

A

^G=^H-T^S

  • G= free energy change KJ
  • H=enthalpy change KJ, calculate using calorimetry and Hess’s law or the enthalpy of formation values
  • T- temperate of system K
  • ^S= entropy change KJ/K, calculate using entropy values
  • If G
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12
Q

Temperature and Thermodynamic favorability

A
^H and ^S: 
- + =yes at all temps
\+ - = no at all temps
- - =yes at low, no at high 
\+ + = yes at high, no at low
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13
Q

Free energy of formation

A

^Grxn=sum n G(products) - Sum n G (reactants)

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14
Q

Find the ^S for the following reactions using the S values given

A

^S=sum n S(products) - sum n S(reactants)

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15
Q

calculate ^G

A

^G=^H-T^S

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16
Q

at what temperature does it become thermodynamically favored?

A

rearrange ^G=^H-T^S and solve where G=0.

17
Q

why can it still be thermodynamically favored when the entropy of the system decreases so dramatically?

A

still exothermic and contributes to the entropy of the universe

18
Q

Find the value of g using the Gf vales

A

^Grxn=sum n G(products) - Sum n G (reactants)

19
Q

Spontaneous signs for G, S, H

A

spontaneous:

  • G -
  • S+
  • H -
20
Q

the G positive at low temps and negative at high temps. predict sign for H

A

negative

21
Q

under what conditions does the is process become thermodynamically favored?

A

when temp is low and G is negative

22
Q

Find S at this temp

A

^G=^H-T^S rearrange to solve for ^S