Entropy

1
Entropy and Free Energy

How to predict if a
reaction can occur,
given enough time?
THERMODYNAMICS
How to predict if a
reaction can occur at a
reasonable rate?
KINETICS
Thermodynamics 2
• If the state of a chemical system is such

that a rearrangement of its atoms and
molecules would decrease the energy of
the system---
• AND the K is greater than 1,
• then this is a product-favored system.

• Most product-favored reactions are
exothermic
—but this is not the only criterion
Thermodynamics 3
• Both product- and reactant-favored reactions can proceed to

equilibrium in a spontaneous process.
AgCl(s) e Ag+(aq) + Cl–(aq)
K = 1.8 x 10-10
Reaction is not product-favored, but it moves
spontaneously toward equilibrium.
• Spontaneous does not imply anything about time for reaction
to occur.
4
Thermodynamics and Kinetics

Diamond is
thermodynamically
favored to convert to
graphite, but not
kinetically favored.
Paper burns — a
product-favored
reaction. Also
kinetically favored once
reaction is begun.
5
Spontaneous Reactions
In general, spontaneous
reactions are
exothermic.
Fe2O3(s) + 2 Al(s) --->
2 Fe(s) + Al2O3(s)
∆H = - 848 kJ
6
Spontaneous Reactions
But many spontaneous reactions or
processes are endothermic or even
have ∆H = 0.
NH4NO3(s) + heat ---> NH4NO3(aq)

Entropy, S
7
One property common to

spontaneous processes is
that the final state is more
DISORDERED or RANDOM
than the original.
Spontaneity is related to
an increase in
randomness.
The thermodynamic property
related to randomness is
Reaction of K
ENTROPY, S.
with water
8
The entropy of
liquid water is
greater than
the entropy of
solid water
(ice) at 0˚ C.
9
Directionality of Reactions
How probable is it that reactant
molecules will react?
PROBABILITY suggests that a
spontaneous reaction will result in
the dispersal
* of energy
* or of matter
* or of energy & matter.
10
Probability suggests that a spontaneous
reaction will result in the dispersal of
energy or of matter or both.
Matter Dispersal
11
Probability suggests that a spontaneous
reaction will result in the dispersal of
energy or of matter or both.
Energy Dispersal
12
Energy Dispersal
Exothermic reactions involve a release of
stored chemical potential energy to the
surroundings.
The stored potential energy starts out in a few
molecules but is finally dispersed over a
great many molecules.
The final state—with energy dispersed—is
more probable and makes a reaction
spontaneous.
13
Entropy, S
So (J/K•mol)
H2O(liq) 69.95
H2O(gas) 188.8
S (gases) > S (liquids) > S (solids)

14
Entropy and States of Matter
S˚(Br2 liq) < S˚(Br2 gas) S˚(H2O sol) < S˚(H2O liq)
15
Entropy, S
Entropy of a substance increases
with temperature.
Molecular motions Molecular motions of
of heptane, C7H16 heptane at different temps.
16
Entropy, S
Increase in molecular
complexity generally
leads to increase in S.
17
Entropy, S
Entropies of ionic solids depend on
coulombic attractions.
So (J/K•mol)
MgO 26.9
NaF 51.5
Mg2+ & O2- Na+ & F-

18
Entropy, S
Entropy usually increases when a
pure liquid or solid dissolves in a
solvent.
19
Standard Molar Entropies
20
Entropy Changes for Phase Changes
For a phase change,

∆S = q/T
where q = heat transferred in
phase change
For H2O (liq) ---> H2O(g)
∆H = q = +40,700 J/mol
Entropy and Temperature 21
S increases
slightly with T
S increases a
large amount
with phase
changes
22
Calculating ∆S for a Reaction

∆So = Σ So (products) - Σ So (reactants)
Consider 2 H2(g) + O2(g) ---> 2 H2O(liq)

∆So = 2 So (H2O) - [2 So (H2) + So (O2)]
∆So = 2 mol (69.9 J/K•mol) -
[2 mol (130.7 J/K•mol) +
1 mol (205.3
J/K•mol)]
∆So = -326.9 J/K
Note that there is a decrease in S because
3 mol of gas give 2 mol of liquid.
23
2nd Law of Thermodynamics
A reaction is spontaneous if ∆S for the
universe is positive.
∆Suniverse = ∆Ssystem + ∆Ssurroundings

∆Suniverse > 0 for spontaneous
process
First calc. entropy created by matter
dispersal (∆Ssystem)
Next, calc. entropy created by energy
dispersal (∆Ssurround)
24
Dissolving NH4NO3 in
water—an entropy
driven process.
∆Suniverse =
∆Ssystem + ∆Ssurroundings
25
2 H2(g) + O2(g) ---> 2 H2O(liq)

∆Sosystem = -326.9 J/K
Can calc. that ∆Horxn = ∆Hosystem = -571.7 kJ
∆Sosurroundings = +1917 J/K

2nd Law of Thermodynamics 26
2 H2(g) + O2(g) ---> 2 H2O(liq) • The entropy of

the universe is
∆Sosystem = -326.9 J/K increasing, so
∆Sosurroundings = +1917 J/K the reaction is
product-favored.
∆Souniverse = +1590. J/K
27
Spontaneous or Not?
Remember that –∆H˚sys is proportional to ∆S˚surr

An exothermic process has ∆S˚surr > 0.

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1

Entropy and Free Energy

• If the state of a chemical system is such

• then this is a product-favored system.

• Both product- and reactant-favored reactions can proceed to

Thermodynamics and Kinetics

NH4NO3(s) + heat ---> NH4NO3(aq)

One property common to

S (gases) > S (liquids) > S (solids)

Entropy and States of Matter

Mg2+ & O2- Na+ & F-

Entropy Changes for Phase Changes

For a phase change,

Calculating ∆S for a Reaction

Consider 2 H2(g) + O2(g) ---> 2 H2O(liq)

∆Suniverse = ∆Ssystem + ∆Ssurroundings

2 H2(g) + O2(g) ---> 2 H2O(liq)

Can calc. that ∆Horxn = ∆Hosystem = -571.7 kJ

∆Sosurroundings = +1917 J/K

2 H2(g) + O2(g) ---> 2 H2O(liq) • The entropy of

Remember that –∆H˚sys is proportional to ∆S˚surr

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