How does the molar entropy of a substance change with increasing temperature?
The molar entropy of a substance increases with increasing temperature.
The value of ∆G° for A →B is greater than zero. What can be concluded for B → A ?
It will be spontaneous, since ∆G° will be negative.
What is the substance being oxidized and reduced?
2Ag(s)+H2S⟶Ag2S(g)+H2(g)
Oxidized: Ag
Reduced: H
What can be concluded about the equilibrium constant (K) for a reaction if ∆G° is negative?
K is greater than 1.
For which will entropy decrease the most?
Zn(s) +Cu2+ (aq) ⇌ Zn2+(aq) + Cu(s)
H2CO3(aq) ⇌ H2O (l) + CO2(g)
Fe3+ (aq) +H2O (l) ⇌ Fe(OH)2+(aq) + H+(aq)
AgCl(s) +Br-(aq) ⇌ AgBr(s) +Cl-(aq)
SO3(g) +H2O(l) ⇌ H+(aq) +HSO4-(aq)
SO3(g) +H2O(l) ⇌ H+(aq) +HSO4-(aq)
Calculate ∆G° for the reaction SO2(g) +2H2(g) → S (s)+ 2H2O (g)
∆G°(SO2(g)) =-300 kJ/mol , ∆G°(H2O (g)) = -230 kJ/mol
-160 kJ/mol
Will the following be spontaneous at constant T and P?
A) ∆H = +25 kJ, ∆S = 5.0 J/K , T=300k
B) ∆H=25 kJ , ∆S=100 J/K , T=300K
A) No
B) Yes
Cr3+ +Cl2 → Cr2O7-2 +Cl-
What is the E° for this reaction?
Use
Cr2O7-2+ 14H+ +6e- → 2Cr3+ +7H2O E°= 1.33
Cl2 +2e- → 2Cl- E° = 1.36
E°cell=0.03
Ni2+(aq) + Zn(s) ⇌ Zn2+ (aq) +Ni(s)
Initial concetrations of [Ni2+] = 1.50 M, [Zn2+ ] = 0.100M. What is initial cell potential?
0.56 V
Which reaction will have entropy increase the most?
Solid ⇌ Liquid
Gas ⇌ Liquid
2H2 (g) + O2(g) ⇌ 2H2O (g)
HCl(g) +NH3(g) ⇌ NH4Cl(s)
2SO2(g) + O2(g) ⇌2SO3(g)
Solid ⇌ Liquid
For the reaction at 298K
2NO2(g) ⇌ N2O4 (g) , ∆H°=-58.03 kJ, ∆S°=-176.6 J/K
What is the value of ∆G° at 298K?
At what temperature will the reach have equilibrium?
∆G°=-5.43 kJ
T=328.6K
At which temperature will the following process be spontaneous?
A) ∆H= -18 kJ and ∆S = -60 J/K
B) ∆H = 18 kJ and ∆S = 60 J/K
C) ∆H= 18 kJ and ∆S = -60 J/k
D) ∆H= -18 kJ and ∆S= 60 J/K
A) Spontaneous less than 300K
B) Spontaneous above 300K
C) Non spontaneous at all temperatures, -300K does not exist.
D) Spontaneous at all temperatures
Is this reaction spontaneous?
MnO4- + I- → I2 + Mn2+
Use
MnO4- +8H+ +5e- → Mn2+ +4H2O E=1.51 V
2I-→ I2 +2e- E=-0.54
Ecell = 0.97 V, yes this is spontaneous
Zn2+ +2e- → Zn E = -0.76
Fe2+ + 2e- → Fe E= -0.44
Calculate E°cell, ∆G°, and K, at 25 Celsius
E°cell = 0.32 v
∆G° = -61750.4 J = -61.75 kJ
K = 6.7 x 1010
C2H4 (g)+ H2O (g)→CH3CH2OH(l)
C2H6(g)+ H2O (g)→CH3CH2OH(l) +H2(g)
Which would be more thermodynamically feasible ?
C2H4 (g)+ H2O (g)→CH3CH2OH(l)
Calculate ∆G° for H2O(g) +0.5O2(g) ⇌H2O2(g) at 600K
use
H2(g) +O2(g) ⇌H2O2(g) K=2.3 x 106
2H2(g) +O2(g) ⇌ 2H2O(g) K = 1.8 x 1037
∆G° = 140.89 kJ/mol
Which process(es) are driven by an increase in the entropy of the surroundings?
A) condensation of water
B)the sublimation of dry ice
C) the freezing of water
A) condensation of water,
C) the Freezing of water
Give the complete reaction and determine Ecell
use
Mn2+ +2e- → Mn E=-1.18 V
Fe3+ + 3e- → Fe E= -0.036
3Mn + 2Fe3+ → 2Fe +3Mn2+
Ecell=3.468
2SO2(g) +O2(g) → 2SO3(g)
At equilibrium partial pressures are pO2 =0.50 atm, pSO3= 2.0. Determine partial pressure of SO2.
∆G°(SO2(g)) =-300 kJ, ∆G°(SO3(g))= -371 kJ
pSO2= 10-12 atm
Predict sign of entropy
A) Si6(aq) +H2 (g) → 2HF (g) +SiF4(g)
B) 4Al(s) +3O2(g) → 2Al2O3(s)
A) +
B) -
Calculate ∆G° for the following reaction:
6C(s) + 3H2(g) →C6H6(l)
given that
2C6H6(l) +15O2→ 12CO2(g) +6H2O(l) ∆G°=-6399 kJ
C(s) + O2(g) → CO2(g) ∆G° = -394 kJ
H2(g) + 0.5O2(g) → H2O (l) ∆G° = -237 kJ
∆G° = 124 kJ
Which process is spontaneous at 298K.
∆G°rxn=8.5
A) H2O (l) → H2O(g, 1 atm)
B) H2O (l) → H2O(g, 0.10 atm)
C) H2O (l) → H2O(g, 0.010 atm)
C) H2O (l) → H2O(g, 0.010 atm)
A galvanic cell is base on these half reactions at 25 Celsius. Predict E given the concentrations, [Ag+] =1.00 M,
[H2O2] = 2.0 M, [H+] = 2.0 M
Ag+ + e-→Ag E=0.80 v
H2O2 + 2H+ + 2e- → 2H2O E=1.78 V
E = 1.01 V approximately
Hgb + O2 → HgbO2 ∆G° =-70 kJ
Hgb + CO → HgbCO ∆G°= -80kJ
Estimate the equilibrium constant at 25 Celsius for:
HgbO2 + CO ⇌ HgbCO + O2
K= 56.60
Determine S° for Fe(CO)5(g) given:
Fe(s)+ 5CO(g) → Fe(CO)5(g) ∆S°= ?
Fe(CO)5(l) → Fe(CO)5(g) ∆S°=107 J/K
Fe(s) + 5CO (g) → Fe(CO)5(l) ∆S°=-677 J/K
S°(CO(g)) =198 J/K, S(Fe(s))= 27 J/K
S°(Fe(CO)5(g))=447 J/K