ELECTROCHEMISTRY

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Some key concepts covered include calculating standard cell potential from half reactions, factors that affect cell potential such as concentration based on Nernst equation, and calculations related to electrolysis including time and mass deposited.

To calculate the standard cell potential, one must first write the balanced half reactions and oxidation/reduction potentials. The cell potential is then calculated as the reduction potential minus the oxidation potential.

According to Nernst equation, the cell potential depends on concentration through a logarithmic term involving the ratio of product and reactant concentrations. Higher concentrations of products or lower concentrations of reactants result in lower (more negative) cell potentials.

Faculty-Wide Courses 2009-2010

ELECTROCHEMISTRY

SHEET 3
1- Consider a galvanic cell based on the reaction
Al+++ (aq) + Mg(s) → Al(s) + Mg++(aq)
E Al    → Al  -1.66 v

EMg 
→Mg
 -2.37 v

Give the balanced cell reaction and calculate E° for the cell.

Since a galvanic cell, so that E° have to be +ve value


1-Half reactions
A-Oxidation Mg++ (aq) + 2 e- → Mg(s) 
EMg 
→Mg
 -2.37 v

Mg(s) → Mg++ (aq) + 2 e- 


EMg →Mg 
 2.37 v

B-Reduction Al+++ (aq) + 3 e- → Al(s) E Al  → Al  -1.66 v

2-Balance the equation


3Mg(s) → 3Mg++ (aq) + 6 e- 
EMg →Mg 
 2.37 v

2Al+++ (aq) + 6 e- → 2Al(s) E Al  → Al  -1.66 v

3-Net equation 3Mg(s) +2Al+++ (aq) →3Mg++ (aq)+ 2Al(s)

4- Ecell = E(Cathod, Reduction) - E (Anode, Oxidation)


E° = (-1.66) – (-2.37) = 0.71 v
Ecell = E(Cathod, Reduction) + E (Anode, Oxidation)
E° = (-1.66) + (2.37) = 0.71 v

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ELECTROCHEMISTRY

2- Describe completely the following galvanic cell based on the following


half reactions.
Cl2 + 2e- → 2 Cl- E°=1.36 v
Br2 + 2e- → 2 Br- E°= 1.09 v

Since a galvanic cell, so that E° have to be +ve value


Note:
As he didn’t give me the final “net” reaction so, I will make assumption which of
the two reaction is will be oxidation “Anode” and which will be reduction “Cathode”,
on my assumption, I will take care that the net value of the E° have to be +ve value
I will assume that the reaction have a E° highest value is the reduction
“Cathode”, and the other is the oxidation “anode” to ensure that the net value of E° is
+ ve value.

1-Half reactions
A-Oxidation Br2 + 2e- → 2 Br- E°= 1.09 v
2 Br- → Br2 + 2e- E°= -1.09 v
B-Reduction Cl2+ 2 e- → 2 Cl - E°= 1.36 v
2-Balance the equation
2 Br- → Br2 + 2e- E°= -1.09 v
Cl2+ 2 e- → 2 Cl - E°=1.36 v

3-Net equation 2 Br + Cl2 → Br2 + 2 Cl -

4- Ecell = E(Cathod, Reduction) - E (Anode, Oxidation)


E° = (1.36) – (1.09) = 0.27 v
Ecell = E(Cathod, Reduction) + E (Anode, Oxidation)
E° = (1.36) + (-1.09) = 0.27 v

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3- Predict whether the following reaction would proceed spontaneously as


written at 298 K.
Co(s) + Fe++ (aq) → Co++ (aq) + Fe(s)
Given that [Co++] =0.15 M and [Fe++] =0.68 M
E = -0.28 v
C o++ → C o

E = -0.44 v
F e++ → F e

1-Half reactions and balance the equation


A-Oxidation Co++ (aq) + 2e- → Co(s) E°= -0.28 v
Co(s) → Co++ (aq) + 2e- E°= 0.28 v
B-Reduction Fe++ (aq) + 2 e- → Fe(s) E°= -0.44 v

2-Net equation Co(s) + Fe++ (aq) → Co++ (aq) + Fe(s)

3- Ecell = E(Cathod, Reduction) - E (Anode, Oxidation)


E° = (-0.44) – (-0.28) = -0.16 v
Ecell = E(Cathod, Reduction) + E (Anode, Oxidation)
E° = (-0.44) + (0.28) = -0.16 v
Dependence of Cell Potential on Concentration
4- Nernest Equation
0.0591
E = E - log( Q)
n
E = -0.16 – (0.0591/ 2) * ( log ( [Co++] / [Fe++] )
E = -0.16 – (0.02955) * ( log ( [0.15] / [0.68] )
E = -0.16 – (0.02955) * ( log ( [0.220588] )
E = -0.16 – (0.02955) * ( -0.65641 )
E = -0.16 – (-0.019397 )
E = -0.140 v
Since the value of E is –ve, so that this is an electrolytic cell
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4- Calculate the EMF for the cell based on the following half reactions
VO2 + 2 H+ + e- → VO++ + H2O E° = 1.00 v
Zn++ + 2 e- → Zn E° = -0.76 v
Where: T=25°C [VO2++] =2.0M
[H+]=0.5M
[VO++] =1.0x10-2M
[Zn++]=1.0x10-1M

See page 839, and 840 in CHEMISTRY ZUMDAHL|ZUMDAHL BOOK


EXAMPLE 18.9

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5- Consider the cell described below:


Zn|Zn++ (1.00M) || Cu++ (1.00 M) |Cu
Calculate the cell potential after the reaction has operated long enough for
the [Zn++] to have changed by 0.2 mol/L. (Assume T=25°C)

1-Half reactions and make the Balance


A-Oxidation Zn++ + 2e- → Zn E°= -0.76 v
Zn → Zn++ + 2e- E°= 0.76 v
B-Reduction Cu+++ 2 e- → Cu E°= 0.34 v

2-Net equation Zn + Cu++ → Cu + Zn++

3- Ecell = E(Cathod, Reduction) - E (Anode, Oxidation)


E° = (0.34) – (-0.76) = 1.1 v
Ecell = E(Cathod, Reduction) + E (Anode, Oxidation)
E° = (0.34) + (0.76) = 1.1 v

Dependence of Cell Potential on Concentration


4- Nernest Equation
0.0591
E = E - log( Q)
n
E = 1.1 – (0.0591/ 2) * ( log ( [ Zn++ ] / [Cu++ ] )
E = 1.1 – (0.02955) * ( log ( [ 200 ] / [1 ] )
E = 1.1 – (0.02955) * ( log ( [ 200] )
E = 1.1 – (0.02955) * ( log ( [ 2] )
E = 1.1 – (8.8 *10-3)
E = 1.091 v

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6- Calculate EMF of the following cell if E Zn++→Zn = -0.76


Zn(s) |Zn++ (aq, 0.1M) ||Zn++ (aq, 1.0M) |Zn(s)

1-Half reactions and make the Balance


A-Oxidation Zn++ + 2e- → Zn E°= -0.76 v
Zn → Zn++ + 2e- E°= 0.76 v
B-Reduction Zn++ + 2e- → Zn E°= -0.76 v

2-Net equation ..... → .....

3- Ecell = E(Cathod, Reduction) - E (Anode, Oxidation)


E° = (-0.76) – (-0.76) = ZERO v
Ecell = E(Cathod, Reduction) + E (Anode, Oxidation)
E° = (-0.76) + (0.76) = ZERO v

Dependence of Cell Potential on Concentration


4- Nernest Equation
0.0591
E = E - log( Q)
n
E = 0 – (0.0591/ 2) * ( log ( [ Zn++ 0.1 M] / [Zn++ 1 M] )
E = 0 – (0.02955) * ( log ( [ 0.1 ] / [1 ] )
E = 0 – (0.02955) * ( log ( [ 0.1] )
E = 0 – (0.02955) * ( -1 )
E = 0.02955 v

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7- Calculate the [Cu++] / [Zn++] ratio at which the following reaction will
become spontaneous at 25°C.
Cu(s) + Zn++ (aq) → Cu++ (aq) + Zn(s)

Reaction to become spontaneous it have to be a galvanic cell, so that the E have a + ve


value
1-Half reactions and make the Balance
A-Oxidation Cu+++ 2 e- → Cu E°= 0.34 v
Cu → Cu+++ 2 e- E°= -0.34 v
B-Reduction Zn++ + 2e- → Zn E°= -0.76 v

2-Net equation Cu + Zn++ → Zn + Cu++

3- Ecell = E(Cathod, Reduction) - E (Anode, Oxidation)


E° = (-0.76) – (0.34) = -1.1 v
Ecell = E(Cathod, Reduction) + E (Anode, Oxidation)
E° = (-0.76) + (-0.34) = -1.1 v

Dependence of Cell Potential on Concentration


4- Nernest Equation
0.0591
E = E - log( Q)
n
E = -1.1 – (0.0591/ 2) * ( log ([Cu++ ] / [ Zn++ ]))
E = -1.1 – (0.02955) * ( log ([Cu++ ] / [ Zn++ ]))
E have a + ve value
-1.1 – (0.02955) * ( log ([Cu++ ] / [ Zn++ ])) > zero
-1.1 > (0.02955) * ( log ([Cu++ ] / [ Zn++ ]))
-1.1 / 0.02955 > ( log ([Cu++ ] / [ Zn++ ]))
-37.225 > ( log ([Cu++ ] / [ Zn++ ]))
10-37.225 > ([Cu++ ] / [ Zn++ ])

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8- Consider the following half reactions


MnO4-(aq) + 8 H+(aq) + 5e- → Mn++(aq) + 4 H2O (L) E°=1.51
NO3-(aq) + 4 H+(aq) + 3 e- → NO(g) + 2 H2O (L) E°=0.96
Predict whether NO3- ions will oxidize Mn2+ to MnO4- under standard
state conditions.

1-Half reactions
A-Oxidation Mn++(aq) + 4 H2O (L)→ MnO4-(aq) + 8 H+(aq) + 5e-
E°= -1.51 v
B-Reduction NO3-(aq) + 4 H+(aq) + 3 e- → NO(g) + 2 H2O (L)
E°=0.96 v
2-Balance the two equation
A-Oxidation 3Mn++(aq) + 12 H2O (L)→ 3MnO4-(aq) + 24 H+(aq) + 15e-
E°= -1.51 v
B-Reduction 5NO3-(aq) + 20 H+(aq) + 15 e- → 5NO(g) + 10H2O (L)
E°=0.96 v
3-Net equation
3Mn++(aq) + 2 H2O (L)+ 5NO3-(aq) → 3MnO4-(aq) + 4 H+(aq)+ 5NO(g)

4- Ecell = E(Cathod, Reduction) - E (Anode, Oxidation)


E° = (0.96) – (1.51) = -0.55 v
Ecell = E(Cathod, Reduction) + E (Anode, Oxidation)
E° = (0.96) + (-1.51) = -0.55 v

Since the value of E is –ve, so that this is an electrolytic cell

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9- How long will it take to plate out 1.0 kg Al from aq Al+++ with a current of
100.0 A? (M.wt. of Al=26.98).

1- Plate out 1.0 kg Al


2- Moles of Al = [Mass/M.wt.Al] = [1.0*1000 gm/ 26.98] = 37.0644 gmole
3-Moles of Electron Al from aq Al+++
1 gmole of Al 3 e-
37.0644 gmole ??? e-

??? e- = 3*37.0644 = 111.193 e-

4- Quantity of charge in coulombs


1e 96,485 coulombs
111.193 e ??? coulombs

??? coulombs = 96,485*111.193 = 10,728,502.59451 coulombs

5-Current and time


Ampere= Coulombs / sec
100.0 A= 10,728,502.59451 coulombs / ??? sec
??? sec = 10,728,502.59451 coulombs / 100 A
??? sec = 10,728,5.02 sec
Time ≈ 30 hr

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10- What mass of Co from aq Co++ can be produced in 1.0 h with a current of
15 A? (M.wt. of Co= 59).

See page 866, in CHEMISTRY ZUMDAHL|ZUMDAHL BOOK QUESTION


NO.91.a

11-An unknown metal M is electrolyzed. It took 74.1 s for a current of 2.00 A


to plate out 0.107 g of the metal from a solution containing M(NO3)3.
Identify the metal.

See page 866, in CHEMISTRY ZUMDAHL|ZUMDAHL BOOK QUESTION


NO.93

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