SME
General Chemistry II

Entropy and Gibbs free energy

Use this for “The ionization of ethanoic acid has ΔG° = +27.1 kJ/mol at 25 °C. Find K.”

Diagram

010203000.250.50.751Extent ξ: pure A (0) to pure B (1)G (kJ/mol)minimum: Q = Kzoom: ξ from 0ξ = 1.79 × 10⁻⁵
−40−2002040−10−8−6−4−20log₁₀ QΔG (kJ/mol)log K = −4.75
K
=
exp(−ΔG°
÷
RT)
=
1.79 ×
10
-5
:
the
minimum
is
at
ξ
=
K
1 + K
=
1.79 ×
10
-5
,
pressed
against
the
edge:
the
inset
magnifies
it,
and
the
line
below
shows
it
at
log
K.
Drawn for a model A ⇌ B with ideal mixing; G of pure A is 0.
This is an example. Type your own values to start a new problem.
ΔG° (kJ/mol)
=
−R
T (K)
ln
K
ln K
Natural log of K
calculated

Formulas

ΔG°
×
1,000
=
−8.314
×
T
×
(ln
K
)
27.1 × 1,000 = −8.314 × 298.15 × (−10.9326)
K
=
e
ln
K
1.79 ×
10
-5
=
e
−10.9326

Assumptions

•
ΔG° = −RT ln K links the free energy change of the reaction with every species in its standard state to K at the same temperature.
•
R = 8.314 J/(mol·K) and ΔG° is in kJ/mol, so ΔG° is multiplied by 1000 to put it in J/mol.
•
ΔG° < 0 means K > 1 (products favored at equilibrium), not that the reaction is fast.
•
Temperatures are in kelvins (°C + 273.15): 25 °C is 298.15 K.

Step-by-step

WE KNOW
ΔG° = +27.1 kJ/mol, T = 298.15 K
FIND
natural log of K (ln K), equilibrium constant (K)
Step 1 · Find natural log of K (ln K)
Use ΔG° × 1,000 = −8.314 × T × (ln K)
Put ΔG° into J/mol, then divide −ΔG° by RT.
ln
K
=
−ΔG°
×
1,000
8.314 ×
T
ln
K
=
−27.1
×
1,000
8.314 × 298.15
ln
K
=
−27.1
×
1,000
2,478.8191
ln
K
=
−
27,100
2,478.8191
ln
K
=
−10.9326
Step 2 · Find equilibrium constant (K)
Use K = eˡⁿᴷ
Undo
the
natural
log:
raise
e
to
ln
K
.
K
=
e
−10.9326
K
=
1.79 ×
10
-5
→
K
<
1:
reactants
are
favored
at
equilibrium.
Check
Put the numbers back in. Both sides should match.
27.1 × 1,000 = −8.314 × 298.15 × (−10.9326) ✓
1.79 ×
10
-5
=
e
−10.9326
✓
Topic check
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