2. Potential Diff bet Zn/Zn2+
Electrode potential Zn/Zn2+
= -ve
-
Electrode Potential
Redox Equilibrium
Zn2+
Zn → Zn 2+
+ 2e
(Oxidation)
Zn 2+
+ 2e → Zn
(Reduction)
Zn 2+
+ 2e ↔ Zn
(At equilibrium)
Metal Zn placed in its sol Zn2+
ion
Equilibrium bet Zn/Zn2+
Zn metal reactive lose e form Zn2+
Equilibrium shift to right ←
Potential Diff form bet Zn/Zn2+
Potential Diff
Electrode potential = -ve
Zn2+
Zn2+
Zn
Zn2+
Zn
Zn2+
Zn2+
Zn2+
Zn 2+
+ 2e ↔ Zn
Equi shift to ←
-
--
Zn
-
-
-
-
+
+
+
+
+ +
+ +
+
Voltage of Zn/Zn2+
can’t be measured.
Abs electrode potential can’t measured.
Only Diff in electrode potential can be measured.
Cannot measure
Abs Potential
Metal Cu placed in its sol Cu2+
ion
Equilibrium bet Cu/Cu2+
Cu2+
ion gain -2e form Cu
Equilibrium shift to left ←
Potential Diff form bet Cu/Cu2+
Potential Diff
Electrode potential = +ve
Cu
Cu2+
Cu2+
Cu2+
Cu2+
Cu → Cu2+
+ 2e
(Oxidation)
Cu2+
+ 2e → Cu
(Reduction)
Cu2+
+ 2e ↔ Cu
(At equilibrium)
Cu
-e
-e
-e
Cu2+
Cu2+
Cu2+
Cu2+
+ 2e ↔ Cu
Equi shift to →
Zn Half Cell
+
+
+
Cu
+
+
+
-
--
-
--- ----
--
Potential Diff bet Cu/Cu2+
Electrode potential Cu/Cu2+
= +ve
Cannot measure
Abs Potential
Voltage of Cu/Cu2+
can’t be measured.
Abs electrode potential can’t measured.
Only Diff in electrode potential can be measured.
PDF version
Online version
Click here chem database
(std electrode potential)
Click here chem database
(std electrode potential)
Click here interactive ECS Click here pdf version ECS
Cu Half Cell
3. Potential Diff Cu/Cu2+
Electrode potential
Cu/Cu2+
= +ve
Potential Diff Zn/Zn2+
Electrode potential
Zn/Zn2+
= -ve
Zn2+
Zn → Zn 2+
+ 2e
(Oxidation)
Zn 2+
+ 2e → Zn
(Reduction)
Zn 2+
+ 2e ↔ Zn
(At equilibrium)
Zn2+
Zn2+
Zn
Zn2+
Zn
Zn2+
Zn2+
Zn2+
Zn 2+
+ 2e ↔ Zn
Equi shift to ←
-
-
-
Zn
-
--
-
+
++
+
+ +
+
+
+
Can’t measure
Abs Potential
Cu
Cu2+
Cu2+
Cu2+
Cu2+
Cu → Cu2+
+ 2e
(Oxidation)
Cu2+
+ 2e → Cu
(Reduction)
Cu2+
+ 2e ↔ Cu
(At equilibrium)
Cu
-e
-e
-e
Cu2+
Cu2+
Cu2+
Cu2+
+ 2e ↔ Cu
Equi shift to →
Zn Half Cell
+
+
+
Cu
+
+
+
-
Cu Half Cell
Zn/Cu Voltaic Cell
External circuit – flow of electrons
Complete circuit
-
--
--
-
-
----
-- -
Connect 2 Half Cell with wire/ salt bridge
Zn half cell (-ve)
Oxidation
Cu half cell (+ve)
Reduction
Salt Bridge – flow of ions
Complete the circuit
Cu2+
+ 2e → CuZn → Zn 2+
+ 2e
Zn + Cu2+
→ Zn2+
+ Cu
Anode Cathode
Maintain electrical
neutrality
Salt bridge – saturated KNO3
Zn2+
increase ↑
NO3
-
flow in to balance excess Zn2+
Cu2+ decrease ↓, excess –ve ion ↑
K+
flow in to balance loss of Cu2+
Zn Cu
--
-
-
Zn2+
Zn2+
Zn2+
Excess of Zn2+
ion
+
+
++
-
-
-
-
---
-
-
-
-
-
Excess of –ve ion
+
+
+
+
++
+
Without Salt Bridge
-+
+
+
+
With Salt Bridge
(electron unable to flow due to ESF)
NO3
-
NO3
-
NO3
-
NO3
-
+
+
+ K
+
K
+
K
+
-
-
-
K+
flow in to balance
excess of – ion
NO3
-
flow in to balance
excess of + ion
2 Half Cell to make a Voltaic Cell
-e -e
-
-
-
-
+
+
+
+
4. Potential Diff Cu/Cu2+
Electrode potential
Cu/Cu2+
= +ve
Potential Diff Zn/Zn2+
Electrode potential
Zn/Zn2+
= -ve
Zn2+
Zn → Zn 2+
+ 2e
(Oxidation)
Zn 2+
+ 2e → Zn
(Reduction)
Zn 2+
+ 2e ↔ Zn
(At equilibrium)
Zn2+
Zn2+
Zn
Zn2+
Zn
Zn2+
Zn2+
Zn2+
Zn 2+
+ 2e ↔ Zn
Equi shift to ←
-
-
-
Zn
-
--
-
+
++
+
+ +
+
+
+
Can’t measure
Abs Potential
Cu
Cu2+
Cu2+
Cu2+
Cu2+
Cu → Cu2+
+ 2e
(Oxidation)
Cu2+
+ 2e → Cu
(Reduction)
Cu2+
+ 2e ↔ Cu
(At equilibrium)
Cu
-e
-e
-e
Cu2+
Cu2+
Cu2+
Cu2+
+ 2e ↔ Cu
Equi shift to →
+
+
+
Cu
+
+
+
-
External circuit – flow of electrons
Complete circuit
-
--
--
-
-
----
-- -
Connect 2 Half Cell with wire/ salt bridge
Zn half cell (-ve)
Oxidation
Cu half cell (+ve)
Reduction
Voltmeter – High resistance
(No current flow) Salt Bridge – flow of ions
Complete the circuit
Cu2+
+ 2e → CuZn → Zn 2+
+ 2e
1.10Volt
Potential diff can be measured.
Voltmeter across – EMF
1.10 Volt
Zn + Cu2+
→ Zn2+
+ Cu
Anode Cathode
Zn(s) | Zn2+
(aq) || Cu2+
(aq)| Cu (s)
Cell diagram
Anode Cathode
Half Cell Half Cell
(Oxidation) (Reduction)
Phase boundarySalt Bridge Flow
electrons
Maintain electrical
neutrality
Salt bridge – saturated KNO3
Zn2+
increase ↑
NO3
-
flow in to balance excess Zn2+
Cu2+ decrease ↓
K+
flow in to balance loss of Cu2+
Zn/Cu Voltaic Cell 2 Half Cell to make a Voltaic Cell
Zn Half Cell Cu Half Cell
-e -e
-
-
-
-
+
+
+
+
5. Potential Diff Ag/Ag2+
Electrode potential
Ag/Ag2+
= +ve
Potential Diff Zn/Zn2+
Electrode potential
Zn/Zn2+
= -ve
Zn2+
Zn → Zn 2+
+ 2e
(Oxidation)
Zn 2+
+ 2e → Zn
(Reduction)
Zn 2+
+ 2e ↔ Zn
(At equilibrium)
Zn2+
Zn2+
Zn
Zn2+
Zn
Zn2+
Zn2+
Zn2+
Zn 2+
+ 2e ↔ Zn
Equi shift to ←
-
-
-
Zn
-
--
-
+
++
+
+ +
+
+
+
Can’t measure
Abs Potential
Ag
Ag+
Ag+
Ag+
Ag+
Ag → Ag+
+ e
(Oxidation)
Ag+
+ e → Ag
(Reduction)
Ag+
+ e ↔ Ag
(At equilibrium)
Ag
-e
-e
-e
Ag+
Ag+
Ag+
Ag+
+ e ↔ Ag
Equi shift to →
+
+
+
Ag
+
+
+
-
External circuit – flow of electrons
Complete circuit
-
--
--
-
-
----
-- -
Connect 2 Half Cell with wire/ salt bridge
Zn half cell (-ve)
Oxidation
Ag half cell (+ve)
Reduction
Voltmeter – High resistance
(No current flow) Salt Bridge – flow of ions
Complete the circuit
Ag+
+ e → AgZn → Zn 2+
+ 2e
1.56Volt
Potential diff can be measured.
Voltmeter across – EMF
1.56 Volt
Zn + 2Ag+
→ Zn2+
+ 2Ag
Anode Cathode
Zn(s) | Zn2+
(aq) || Ag+
(aq)| Ag (s)
Cell diagram
Anode Cathode
Half Cell Half Cell
(Oxidation) (Reduction)
Phase boundarySalt Bridge Flow
electrons
Maintain electrical
neutrality
Salt bridge – saturated KNO3
Zn2+
increase ↑
NO3
-
flow in to balance excess Zn2+
Ag+ decrease ↓
K+
flow in to balance loss of Ag+
Zn/Ag Voltaic Cell 2 Half Cell to make a Voltaic Cell
Zn Half Cell Ag Half Cell
Ag
Ag+
-e -e
-
-
-
-
+
+
+
+
6. Potential Diff Ag/Ag2+
Electrode potential
Ag/Ag2+
= +ve
Potential Diff Cu/Cu2+
Electrode potential
Cu/Cu2+
= -ve
Cu2+
Cu → Cu 2+
+ 2e
(Oxidation)
Cu 2+
+ 2e → Cu
(Reduction)
Cu 2+
+ 2e ↔ Cu
(At equilibrium)
Cu2+
Cu2+
Cu
Cu2+
Cu
Cu2+
Cu2+
Cu2+
Cu 2+
+ 2e ↔ Cu
Equi shift to ←
-
-
-
Cu
-
--
-
+
++
+
+ +
+
+
+
Can’t measure
Abs Potential
Ag
Ag+
Ag+
Ag+
Ag+
Ag → Ag+
+ e
(Oxidation)
Ag+
+ e → Ag
(Reduction)
Ag+
+ e ↔ Ag
(At equilibrium)
Ag
-e
-e
-e
Ag+
Ag+
Ag+
Ag+
+ e ↔ Ag
Equi shift to →
+
+
+
Ag
+
+
+
-
External circuit – flow of electrons
Complete circuit
-
--
--
-
-
----
-- -
Connect 2 Half Cell with wire/ salt bridge
Cu half cell (-ve)
Oxidation
Ag half cell (+ve)
Reduction
Voltmeter – High resistance
(No current flow) Salt Bridge – flow of ions
Complete the circuit
Ag+
+ e Ag→Cu → Cu 2+
+ 2e
0.46Volt
Potential diff can be measured.
Voltmeter across – EMF
0.46 Volt
Cu + 2Ag+
→ Cu2+
+ 2Ag
Anode Cathode
Cu(s) | Cu2+
(aq) || Ag+
(aq)| Ag (s)
Cell diagram
Anode Cathode
Half Cell Half Cell
(Oxidation) (Reduction)
Phase boundarySalt Bridge Flow
electrons
Maintain electrical
neutrality
Salt bridge – saturated KNO3
Cu2+
increase ↑
NO3
-
flow in to balance excess Cu2+
Ag+ decrease ↓
K+
flow in to balance loss of Ag+
Cu/Ag Voltaic Cell 2 Half Cell to make a Voltaic Cell
Cu Half Cell Ag Half Cell
Ag
Ag+
Cu
Cu2+
-e -e
-
-
-
-
+
+
+
+
7. Standard Electrode Potential
Standard Hydrogen Electrode (SHE)
Platinum coat with Platinum oxide/black
– increase surface area for adsorption H2
- catalyze equilibrium bet H2 /H+
- H2 ↔ 2H+
+ 2e-
Eθ
Standard Reference electrode
All Cell Potential are measured against
• Conc ( 1M)
• Pressure (1 atm)
• Temp (298K)
• Platinum- inert electrode
(sys without metal)
Standard
condition
H2 at 1 atm
Platinum
H2 gas
Pt wire
Platinum
2H+
+ 2e ↔ H2
Eθ
= 0V
Types of Half Cells
Metal/ Ion (M/M+
)
Gas/ Ion (M/M-
)
Ion/ Ion (Fe3+
/Fe2+
)
• Pure Zn metal
• Conc (1M Zn2+
)
• Pressure (1 atm)
• Temp (298K)
Condition Std Zn/Zn2+
Condition Std CI2/CI-
• CI2 gas
• Platinum electrode
• Conc (1M CI-
)
• Pressure (1 atm)
• Temp (298K)
• Platinum electrode
• Conc (1M Fe3+
/Fe2+
)
• Pressure (1 atm)
• Temp (298K)
Condition Std Fe3+
/ Fe2+
Zn2+
Zn
Fe3+
/Fe2+
CI-
Condition for Standard
C
A
N
T
M
E
A
S
U
R
E
A
B
S
P
O
T
E
N
T
I
A
L
1
2
3
How to measure
electrode
potential ?
Pt
1M H+
Measure
Difference?
8. Standard Electrode Potential
Std Hydrogen Electrode (SHE)
Eθ
= 0V
Types of Half Cells
Metal/ Ion (M/M+)
Gas/ Ion (M/M+
)
Ion/ Ion (Fe3+
/Fe2+
)
• Pure Zn metal
• Conc (1M Zn2+
)
• Pressure (1 atm)
• Temp (298K)
Condition Std Zn/Zn2+
Condition Std CI2/CI-
• CI2 gas
• Platinum electrode
• Conc (1M CI-
)
• Pressure (1 atm)
• Temp (298K)
• Platinum electrode
• Conc (1M Fe3+
/Fe2+
)
• Pressure (1 atm)
• Temp (298K)
Condition Std Fe3+
/ Fe2+
Zn2+
Zn
Fe3+
/Fe2+
1
2
3
Connect to SHE
Connect to SHE
Connect to SHE
Eθ
= 0V
Eθ
= 0V
Eθ
= -0.76V
Standard electrode potential Zn/Zn2+
= -0.76V
Eθ
cell = -0.76V
Eθ
= +0.77V
Eθ
= +1.35V
Standard electrode potential Fe3+
/Fe2+
= +0.77V
Eθ
cell = +0.77V
Standard electrode potential CI2 /CI-
= +1.35V
Eθ
cell = +1.35V
Eθ
= -0.76V
Eθ
= +0.77V
Eθ
= +1.35V
2 Half Cell with SHE as reference electrode
CI-
Pt
+
+
+
Pt
36. Eθ
value DO NOT depend surface area of metal electrode.
EMF = Energy per unit charge. (Joule)/C
EMF 10v = 10J energy released by 1C of charge flowing
= 100J energy released by 10C of charge flowing
Eθ
– intensive property– independent of amt – ratio energy/charge
Increasing surface area metal will NOT increase EMF
Eθ
Zn/Cu = 1.10V
Surface area exposed 10 cm2
Total charges 100C leave electrode
EMF = 1.10V = 1.1 J energy for 1 C (charges leaving)
1C release 1.1J energy
100 C release 110 J energy
Voltmeter measure energy for 1C – 110J/100C – 1.1V
EMF no change
Current – measured in Amperes or Coulombs per second
1A = 1 Coulomb charge pass through a point in 1 second = 1C/s
1 Coulomb charge (electron) = 6.28 x 10 18
electrons passing in 1 second
1 electron/proton carry charge of – 1.6 x 10 -19 C ( very small)
6.28 x 10 18
electron carry charge of - 1 C
ond
electron
ond
Coulomb
A
sec.1
.1028.6
sec1
1
1
18
×
==
Surface area increase ↑
Total Energy increase ↑
Total Charge increase ↑Current increase ↑
BUT EMF remain SAME
EMF = (Energy/charge)
t
Q
I
tIQ
=
×=
Q up ↑ – I up ↑
100C flow
110J released
VEMF
EMF
eCh
Energy
EMF
10.1
100
110
arg
=
=
=
Surface area exposed 10 cm2
Surface area exposed 100cm2
Surface area exposed 100 cm2
Total charges 1000C leave electrode
EMF = 1.10V = 1.1 J energy for 1 C (charges leaving)
1C release 1.1J energy
1000 C release 1100 J energy
Voltmeter measure energy for 1C – 1100J/1000C – 1.1V
EMF no change
VEMF
EMF
eCh
Energy
EMF
10.1
1000
1100
arg
=
=
=
Eθ
Zn/Cu = 1.10V
1000C flow
1100J released
t
Q
I =
t
Q
I =
37. Iron rust in presence of water + oxygen
Iron galvanized/coated with zinc.
Oxidized sp ↔ Reduced sp Eθ
/V
Zn2+
+ 2e- Zn↔ - 0.76
Fe2+
+ 2e- ↔ Fe -0.44
O2 + 2H2O + 4e ↔ 4OH-
+0.40
Iron rusting
Rusting Process happen
Eθ
/V
Fe2+
+ 2e- ↔ Fe -0.44
O2 + 2H2O + 4e ↔ 4OH-
+0.40
O2 + 4H+
+ 4e ↔ 2H2O + 1.23
H2O + O2 less reactive (cathode region) – reduction – gain e
Fe more reactive (anode region) – oxidation - lose e
OxidationReduction
Fe2+
+ 2e- Fe -0.44↔
O2 +2H2O+4e ↔ 4OH-
+0.40
Fe Fe↔ 2+
+ 2e Eθ
= +0.44
O2+2H2O+4e ↔ 4OH-
Eθ
= +0.40
2Fe+O2 +2H2O→2Fe2+
+4OH-
Eθ
= +0.84V
Eθ
= +0.84V +ve (spontaneous)
О
О
Dissolve O2
in water
Dissolve O2
in acid
How galvanizing reduces rusting
Iron Galvanized
with Zn
Iron/Steel Galvanized
with tin
Zn more reactive – lose e instead of Fe
Zn as Sacrificial metal/ Cathodic Protection
Electron flow to O2/H2O region
Prevent Fe rusting/lose e
O2 gain e
Fe
O2 + 2H2O + 4e ↔ 4OH-
flow e-
Zn oxidation/lose e
Zn2+
+ 2e- ↔ Zn -0.76
O2 +2H2O+4e ↔ 4OH-
+0.40
Zn lose e- (Stronger RA)
Zn ↔ Zn2+
+ 2e Eθ
= +0.76
O2+2H2O+4e ↔ 4OH-
Eθ
= +0.40
2Zn+O2 +2H2O→2Zn2+
+4OH-
Eθ
= +1.16V
Eθ
= +1.16 +ve (spontaneous)
water
О
О
Anodic region
Cathodic region
Zn Zn
FeFeFe
38. Eθ
= +0.84V +ve (spontaneous)
Iron rust in presence of water + oxygen
Iron can coated with tin widely used in canning
Tin corrodes less readily than iron (protect iron)
Oxidized sp ↔ Reduced sp Eθ
/V
Fe2+
+ 2e- ↔ Fe -0.44
Sn2+
+ 2e- Sn -0.14↔
O2 + 2H2O + 4e ↔ 4OH-
+0.40
Iron rusting
If tin coat broken, iron rust faster as it will displace tin ions from its solution
Will iron rust spontaneously, if Sn2+
(tin ions) are formed.
Rusting Process happen
Eθ
/V
Fe2+
+ e- ↔ Fe -0.44
O2 + 2H2O + 4e ↔ 4OH-
+0.40
O2 + 4H+
+ 4e ↔ 2H2O + 1.23
H2O + O2 less reactive (cathode region) – reduction – gain e
Fe more reactive (anode region) – oxidation - lose e
OxidationReduction
Fe2+
+ 2e- Fe -0.44↔
O2 +2H2O+4e ↔ 4OH-
+0.40
Fe Fe↔ 2+
+ 2e Eθ
= +0.44
O2+2H2O+4e ↔ 4OH-
Eθ
= +0.40
2Fe+O2 +2H2O 4Fe→ 2+
+4OH-
Eθ
= +0.84V
Eθ
= +0.84V +ve (spontaneous)
О
О
Dissolve O2
in water
How coating reduces rusting
Iron/Steel coated with tin/Sn
BUT if it is exposed - Fe will rust
Fe more reactive Sn
Tin/Sn protect Fe metal
Electron flow Fe to O2/H2O region
water
Fe oxidation/lose e
flow e-
O2 + 2H2O + 4e ↔ 4OH-
Iron metal
water
O2 gain e
Sn Sn2+
Oxidized sp ↔ Reduced sp Eθ
/V
Fe2+
+ 2e- ↔ Fe -0.44
Sn2+
+ 2e- Sn -0.14↔
O2 + 2H2O + 4e ↔ 4OH-
+0.40
Fe Fe↔ 2+ + 2e Eθ = +0.44
O2+2H2O+4e ↔ 4OH-
Eθ
= +0.40
2Fe+O2 +2H2O 4Fe→ 2+
+4OH-
Eθ
= +0.84V
Fe Fe↔ 2+ + 2e Eθ = +0.44
Sn2+
+ 2e ↔ Sn Eθ
= -0.14
Fe + Sn2+
→ Fe2+
+ Sn Eθ
= +0.30V
Eθ
= +0.30V +ve (spontaneous)
О
О
О
О
Sn SnSn
FeFeFe Fe
39. State which is able to convert Fe2+
to Fe3+
Oxidized sp ↔ Reduced sp Eθ
/V
AI3+
+ 3e- AI -1.66↔
I2 + 2e- ↔ 2I-
+0.54
Fe3+
+ e- ↔ Fe2+
+0.77
H2O2 + 2H+
+ 2e ↔ 2H2O +1.07
Co3+
+ e ↔ Co2+
+1.51
2Fe2+
2Fe↔ 3+
+ 2e Eθ
= -0.77
H2O2 + 2H+
+ 2e 2H↔ 2O Eθ
=+1.07
2Fe2+
+ H2O2 + 2H+
2Fe→ 3+
+ 2H2O Eθ
= +0.30V
Eθ
= +0.30 +ve (spontaneous)
Fe2+
Fe↔ 3+
+ e Eθ
= -0.77
Co3+
+ e ↔ Co 2+
Eθ
=+1.51
Fe2+
+ Co3+
Fe→ 3+
+ Co2+
Eθ
= +0.74V
Eθ
= +0.74 +ve (spontaneous)
Eθ
cell = EMF in V (std condition)
Eθ
= Show ease/tendency of species to accept/lose electron
Eθ
= +ve std electrode potential = stronger oxidizing agent – weaker reducing agent – accept e
Eθ
= - ve std electrode potential = stronger reducing agent - weaker oxidizing agent – lose e
EMF when half cell connect to SHE std condition
Std potential written as std reduction potential
Eθ value DO NOT depend on stoichiometric coefficient. EMF = Energy per unit charge. (Joule)/C
EMF 10v = 10J energy released by 1C of charge flowing
= 100J energy released by 10C of charge flowing
Eθ
, Std electrode potential – intensive property – not dependent on amt – ratio energy/charge
Eθ
= +ve suggest rxn feasible, does not tell rate, feasible but may be slow, give no indication rate
Eθ
= +ve = Energetically feasible but kinetically non feasible
E = ↑ +ve ↑ (OA)
Oxidized sp ↔ Reduced sp Eθ
/V
Fe3+
+ e- ↔ Fe2+
+0.77
H2O2 +2H+
+2e ↔ 2H2O +1.07
Oxidized sp ↔ Reduced sp Eθ
/V
Fe3+
+ e- ↔ Fe2+
+0.77
Co3+
+ e ↔ Co2+
+1.51
Stronger OA
Strongest OA
Redox Question
Aluminium air battery
Excellent Zn/Cu gravity cell for IA
Zinc air battery
Videos on battery making
40. Arrange the species in order of
increasing oxidizing/reducing strength
Oxidized sp ↔ Reduced sp Eθ
/V
Zn2+
+ 2e- Zn -0.76↔
Br2 + 2e- ↔ 2Br-
+1.07
I2 + 2e- ↔ 2I-
+0.54
Fe3+
+ e- ↔ Fe2+
+0.77
MnO4
-
+ 8H+
+ 5e- ↔ Mn2+
+ 4H2O +1.51
Oxidizing agent (OA)
MnO4
_
> Br2 > Fe3+
> I2 > Zn2+
Reducing agent (RA)
Zn > I-
> Fe 2+
> Br-
> Mn2+
Arrange in order of increasing reducing strength.
(Strongest reducing agent)
Redox Questions
1 2
E = most +ve ↑
strongest OA
E = most -ve ↑
strongest RA
Oxidized sp ↔ Reduced sp Eθ
/V
Zn2+
+ 2e- Zn -0.76↔
I2 + 2e- ↔ 2I-
+0.54
Fe3+
+ e- ↔ Fe2+
+0.77
Br2 + 2e- ↔ 2Br-
+1.07
MnO4
-
+ 8H+
+ 5e- ↔ Mn2+
+ 4H2O +1.51
arrange increasing ↑ E value
E = ↑ +ve ↑ (OA)
Eθ
/V
X 3+
+ 3e- X -1.56↔
Y 2+
+ 2e- Y -2.70↔
Z 2+
+ 2e- Z +0.90↔
E = ↑ -ve ↑(RA)
E = most -ve ↑
strongest RA
Reducing agent
Y > X > Z
arrange increasing ↑ E value
Eθ
/V
Y 2+
+ 2e- Y -2.70↔
X 3+
+ 3e- X -1.56↔
Z 2+
+ 2e- Z +0.90↔
E = ↑ -ve ↑ (RA)
4433
Oxidized sp ↔ Reduced sp Eθ
/V
Ti2+
+ 2e- Ti -1.63↔
2H+
+ 2e- H↔ 2 0.00
Rxn bet Ti + H+
Will it happen ?
Ti Ti↔ 2+
+ 2e Eθ
= +1.63
2H+
+ 2e H↔ 2 Eθ
= 0.00
Ti + 2H+
Ti→ 2+
+ H2 Eθ
= +1.63V
Eθ
= +1.63V
+ve (spontaneous)
What happen when gold added to acid
Oxidized sp ↔ Reduced sp Eθ
/V
2H+
+ 2e- H↔ 2 0.00
Au3+
+ 3e ↔ Au +1.58
Rxn bet Au + H+
Will it happen ?
What happen when titanium added to acid
2Au 2↔ Au3+
+ 6e Eθ
= -1.58
6H+
+ 6e 3H↔ 2 Eθ
= 0.00
2Au + 6H+
2Au→ 3+
+ 3H2 Eθ
= -1.58V
Eθ
= -1.58V
-ve ( NON spontaneous)
acid acid
41. Redox Question
6Predict if manganate will oxidize chloride ion?
MnO2 + 4H+
+ 2CI-
Mn→ 2+
+ 2H2O + CI2 Eθ
= ?
55
MnO2 +4H+
+ 2e- Mn↔ 2+
+ 2H2O +1.23
1/2CI2 + e- ↔ CI-
+1.36
2CI-
CI↔ 2 + 2e Eθ
= -1.36
MnO2 + 4H+
+ 2e Mn↔ 2+
+ 2H2O Eθ
= +1.23
MnO2 + 4H+
+2CI-
Mn→ 2+
+2H2O+CI2 Eθ
= -0.13V
Eθ
= -0.13V -ve (NON spontaneous)
Oxidized sp ↔ Reduced sp Eθ
/V
Cr2O7
2-
+ 14H+
+ 6e- ↔ 2Cr3+
+ 7H2O +1.33
MnO2 +4H+
+ 2e- Mn↔ 2+
+ 2H2O +1.23
1/2CI2 + e- ↔ CI-
+1.36
MnO4
-
+ 8H+
+ 5e- ↔ Mn2+
+ 4H2O +1.51
Predict if MnO4
-
able to oxidize aq CI-
to CI2
2MnO4 + 16H+
+ 10CI-
2Mn→ 2+
+ 8H2O + 5CI2
E = ↑ +ve ↑ (OA)О
О
Oxidized sp ↔ Reduced sp Eθ
/V
Cr2O7
2-
+ 14H+
+ 6e- ↔ 2Cr3+
+ 7H2O +1.33
MnO2 +4H+
+ 2e- Mn↔ 2+
+ 2H2O +1.23
1/2CI2 + e- ↔ CI-
+1.36
MnO4
-
+ 8H+
+ 5e- ↔ Mn2+
+ 4H2O +1.51
О
О
2CI-
CI↔ 2 + 2e Eθ
= -1.36
MnO4
-
+ 8H+
+ 5e Mn↔ 2+
+ 4H2O Eθ
= +1.51
2MnO4 + 16H+
+10CI-
2Mn→ 2+
+8H2O+5CI2 Eθ
= +0.15V
1/2CI2 + e- ↔ CI-
+1.36
MnO4
-
+ 8H+
+ 5e- ↔ Mn2+
+ 4H2O +1.51
Eθ
= +0.15V +ve (spontaneous)
Predict if iron react with HCI a) absence air
Which is stronger OA ?
Fe Fe↔ 2+
+ 2e Eθ
= +0.44
2H+
+ 2e H↔ 2 Eθ
= 0.00V
Fe + 2H+
Fe→ 2+
+ H2 Eθ
= +0.44V
Eθ
= +0.44V +ve (spontaneous)
Oxidized sp ↔ Reduced sp Eθ
/V
Fe2+
+ 2e- Fe -0.44↔
2H+
+ 2e- H↔ 2 0.00
O2 +2H2O+4e ↔ 4OH-
+0.40
Fe Fe↔ 2+
+ 2e Eθ
= +0.44
O2+2H2O+4e ↔ 4OH-
Eθ
= +0.40
2Fe+O2 +2H2O→2Fe2+
+4OH-
Eθ
= +0.84V
Predict if iron react with HCI b) presence of air
Fe2+
+ 2e- Fe -0.44↔
2H+
+ 2e- H↔ 2 0.00
О
О
Fe2+
+ 2e- Fe -0.44↔
O2 +2H2O+4e ↔ 4OH-
+0.40
О
О
Oxidized sp ↔ Reduced sp Eθ
/V
Fe2+
+ 2e- Fe -0.44↔
2H+
+ 2e- H↔ 2 0.00
O2 +2H2O+4e ↔ 4OH-
+0.40
Eθ
= +0.84V +ve (spontaneous)
Iron rusting
E = ↑ +ve
↑ (OA)
42. Acknowledgements
Thanks to source of pictures and video used in this presentation
Thanks to Creative Commons for excellent contribution on licenses
http://creativecommons.org/licenses/
http://spmchemistry.onlinetuition.com.my/2013/10/electrolytic-cell.html
http://www.chemguide.co.uk/physical/redoxeqia/introduction.html
http://educationia.tk/reduction-potential-table
http://2012books.lardbucket.org/books/principles-of-general-chemistry-v1.0/s23-
electrochemistry.html
http://wps.prenhall.com/wps/media/objects/4680/4792445/ch18_10.htm
Prepared by Lawrence Kok
Check out more video tutorials from my site and hope you enjoy this tutorial
http://lawrencekok.blogspot.com