Definitions [11]
Any reaction that involves both oxidation and reduction occurring simultaneously is called an oxidation-reduction reaction or simply a redox reaction.
or
The chemical reaction in which both oxidation and reduction occur simultaneously is called a redox reaction.
The species which gets itself oxidised and reduce another species is called reducing agent.
or
A substance which involves an increase in the oxidation number of one or more of its elements. A reducing agent helps reduce the other substance by being oxidised.
\[\begin{aligned} & \mathrm{ZnO}+\mathrm{C}\longrightarrow\mathrm{Zn}+\mathrm{CO} \\ & \mathrm{Reducing} \\ & \mathrm{agent} \end{aligned}\]
The species which gets itself reduced and oxidise another species is called oxidising agent.
or
A substance which involves a decrease in the oxidation number of one or more of its elements. An oxidising agent helps oxidise the other substance by being reduced itself.
\[\begin{aligned} & \mathrm{S}+6\mathrm{HNO}_{3}\longrightarrow\mathrm{H}_{2}\mathrm{SO}_{4}+2\mathrm{H}_{2}\mathrm{O}+6\mathrm{NO}_{2} \\ & \mathrm{Oxidising} \\ & \mathrm{agent} \end{aligned}\]
"Reduction" is defined as the removal of oxygen/ electronegative element from a substance or the addition of hydrogen/Electron/ electropositive element to a substance.
or
A process involving decrease in oxidation number by gain of electrons.
"Oxidation" is defined as the addition of oxygen/electronegative element to a substance or the removal of hydrogen/ Electron/ electropositive element from a substance.
or
A process involving an increase in oxidation number by the loss of electrons.
Electrochemistry is the branch of chemistry that deals with the production of electricity from the energy released during spontaneous reactions and the use of electrical energy to drive non-spontaneous reactions.
Oxidation number (also called oxidation state) is the charge that an atom of an element appears to have when present in a combined state with other atoms. It is a hypothetical charge assigned by assuming all bonds are ionic — atoms in real molecules like H₂O do not actually carry these charges.
Define the following term:
Kohlrausch’s Law.
It states that at infinite dilution, the molar conductance of an electrolyte is the sum of molar conductances of its ions with molar conductance of each ion multiplied with the number of ions present in the formula of the electrolyte.
Define the following term:
Fuel cell
Fuel cells are the galvanic cells in which the energy of combustion of fuels like hydrogen, methanol, etc., is directly converted into electrical energy.
Define anode
The electrode at which the oxidation occur is called anode.
Define cathode
The electrode at which the reduction occur is called cathode.
Theorems and Laws [2]
The limiting molar conductivity of an electrolyte (i.e., molar conductivity at infinite dilution) is the sum of the limiting ionic conductivities of the cation and the anion, each multiplied by the number of ions present in one formula unit of electrolyte.
\[\Lambda_{m}\operatorname{for}A_{x}B_{y}=x\mathrm{l}_{(A)}{}^{0y+}+yl_{(B)}{}^{0x-}\]
Where l°A and l°B are the limiting ionic conductivities of the cation and anion.
Faraday's laws of electrolysis are quantitative laws that describe the effects of electrolysis. They are:
First Law: The mass of any substance deposited or liberated at any electrode is directly proportional to the quantity of electricity passed through the electrolyte.
W ∝ Q
W = ZQ (Z = electrochemical equivalent)
W = ZIt
\[(Z=\frac{\text{Equivalent Weight}}{96500})\]
Second Law: When the same quantity of electricity is passed through solutions of different electrolytes connected in series, the weight of substances produced at the electrodes is directly proportional to their equivalent weights.
\[\frac{\text{Weight of }M_1\mathrm{~Deposited}}{\text{Weight of }M_2\mathrm{~Deposited}}=\frac{\text{Eq. wt. of }M_1}{\text{Eq. wt. of }M_2}\cdots\cdots\]
Key Points
Redox Reactions:
- A substance that oxidises another substance (and is itself reduced) is called an oxidising agent.
- A substance that reduces another substance (and is itself oxidised) is called a reducing agent.
What is Oxidation and Reduction?
| Perspective | Oxidation | Reduction |
|---|---|---|
| In terms of oxygen | Gain of one or more O atoms | Loss of one or more O atoms |
| In terms of hydrogen | Loss of hydrogen | Gain of hydrogen |
| In terms of electropositive element | Loss of electropositive element | Gain of electropositive element |
| In terms of electronegative element | Gain of electronegative element | Loss of electronegative element |
| In terms of electrons | Loss of electrons | Gain of electrons |
| In terms of oxidation number | Increase in oxidation number | Decrease in oxidation number |
Redox in Terms of Electron Transfer:
A reaction in which electrons are lost by one substance and gained by another is called a redox reaction.
- Oxidising agent = electron acceptor
- Reducing agent = electron donor
Example:
(Hg₂²⁺ gains electrons → reduced; Sn²⁺ loses electrons → oxidised)
| Feature | Metallic Conductors | Electrolytic Conductors |
|---|---|---|
| Charge Carriers | Free electrons | Ions (cations and anions) |
| Medium | Solid metals | Molten state or aqueous solution |
| Conduction Mechanism | Movement of electrons | Movement of ions |
| Type of Ions | No ions involved | Positive (cations) and negative (anions) |
| Effect of Temperature | Conductance decreases with an increase in temperature | Conductance increases with an increase in temperature |
| Examples | Copper, Aluminium | NaCl solution, molten salts |
Electrical conductance and resistance:
\[\mathrm{K}=\mathrm{G}\frac{l}{A}\]
K = Conductivity
G = Conductance
\[\mathrm{G}=\mathrm{}\frac{1}{R}\]
R = Resistance
\[\mathrm{K}=\mathrm{}\frac{l}{RA}\]
Rules for Assigning Oxidation Numbers:
| Species | Rule |
|---|---|
| Free elements | Oxidation number = 0 (e.g., Na, O₂, O₃, Hg, S₈, P₄) |
| Monoatomic ions | Oxidation number = charge on the ion (e.g., Mn²⁺ = +2, Cr³⁺ = +3) |
| Fluorine | Always −1 in all compounds |
| Oxygen | Usually −2; Exceptions: −1 in peroxides (H₂O₂), −1/2 in superoxides (KO₂), +2 in oxygen fluoride (OF₂) |
| Hydrogen | Usually +1; Exception: −1 in metal hydrides (e.g., CaH₂, NaH) |
| Halogens (Cl, Br, I) | Usually −1 in binary compounds; can be positive when bonded to a more electronegative element or oxygen |
| Neutral compound | Sum of all oxidation numbers = 0 |
| Polyatomic ion | Sum of all oxidation numbers = charge on the ion |
- Oxidation number of N can be −3 (bonded to less electronegative atoms) or +3 (bonded to more electronegative atoms)
- Oxidation number of halogens is always −1 in metal halides
- In interhalogen compounds, the more electronegative halogen gets the oxidation number of −1
- Oxidation number of metals in amalgams and carbonyls is zero (e.g., Fe in [Fe(CO)₅] = 0)
- In complex ions, the algebraic sum of oxidation numbers of all atoms = net charge on the ion
- Oxidation number can be positive, negative, zero, a whole number, or a fraction
- Oxidation number greater than +6 or less than −4 is unusual — double-check for errors
Stock Notation
Variable oxidation states are indicated using Roman numerals in parentheses after the element symbol:
| Formula | Name | Stock Notation |
|---|---|---|
| Cu₂O | Cuprous oxide | Copper (I) oxide |
| Fe₂O₃ | Ferric oxide | Iron (III) oxide |
| HgCl₂ | Mercuric chloride | Mercury (II) chloride |
| SnCl₂ | Stannous chloride | Tin (II) chloride |
| Type | Core Idea | General Form | Key Feature | Example |
|---|---|---|---|---|
| Combination Reaction | Two or more reactants combine to form one product | A + B → AB | Single product formed | C + O₂ → CO₂ |
| Decomposition Reaction | One compound breaks into simpler substances | AB → A + B | Reverse of combination | 2NaH → 2Na + H₂ |
| Displacement Reaction | More reactive element displaces less reactive element | X + YZ → XZ + Y | Based on reactivity series | Zn + CuSO₄ → ZnSO₄ + Cu |
| a) Metal Displacement | Metal replaces another metal in compound | M₁ + M₂X → M₁X + M₂ | More reactive metal displaces less reactive | Zn + CuSO₄ → ZnSO₄ + Cu |
| b) Non-metal Displacement | Non-metal replaces another non-metal | X₂ + 2Y⁻ → 2X⁻ + Y₂ | Less common, includes H displacement | 2Na + 2H₂O → 2NaOH + H₂ |
| Disproportionation Reaction | Same element is oxidized and reduced | A → A⁺ + A⁻ | One element, two oxidation states | 2H₂O₂ → 2H₂O + O₂ |
Two methods are used to balance redox reactions:
Method 1: Oxidation Number Method
The change in oxidation number is used to balance electron gain and loss.
Steps (Acidic Medium):
- Write the skeleton equation; balance all atoms except O and H first
- Identify which atoms change oxidation number; calculate the net increase and decrease
- Multiply coefficients to make total increase in oxidation number = total decrease
- Balance O atoms by adding H₂O to the side with fewer O atoms
- Balance H atoms by adding H⁺ ions
- Check that all atoms and charges are balanced
Method 2: Ion Electron Method (Half-Reaction Method)
The reaction is split into two half-reactions (oxidation and reduction) which are balanced separately and then combined.
Steps:
- Write the redox reaction in ionic form
- Split into oxidation half-reaction and reduction half-reaction
- Balance atoms in each half-reaction (except O and H first)
- Balance O by adding H₂O; balance H by adding H⁺ (acidic) or OH⁻ (basic)
- Balance charge by adding electrons to the appropriate side
- Equalise electrons transferred — multiply one or both half-reactions by suitable factors so electrons cancel
- Add both half-reactions; cancel identical species on both sides
- Check that all atoms and charges are balanced
For Basic Medium (Ion Electron Method):
After balancing in acidic conditions:
- Add OH⁻ ions to both sides equal to the number of H⁺ ions
- H⁺ + OH⁻ → H₂O (combine)
- Eliminate H₂O molecules appearing on both sides
- Final check: all elements and charges must balance
Two methods are used to balance redox reactions:
Method 1: Oxidation Number Method
The change in oxidation number is used to balance electron gain and loss.
Steps (Acidic Medium):
- Write the skeleton equation; balance all atoms except O and H first
- Identify which atoms change oxidation number; calculate the net increase and decrease
- Multiply coefficients to make total increase in oxidation number = total decrease
- Balance O atoms by adding H₂O to the side with fewer O atoms
- Balance H atoms by adding H⁺ ions
- Check that all atoms and charges are balanced
Method 2: Ion Electron Method (Half-Reaction Method)
The reaction is split into two half-reactions (oxidation and reduction) which are balanced separately and then combined.
Steps:
- Write the redox reaction in ionic form
- Split into oxidation half-reaction and reduction half-reaction
- Balance atoms in each half-reaction (except O and H first)
- Balance O by adding H₂O; balance H by adding H⁺ (acidic) or OH⁻ (basic)
- Balance charge by adding electrons to the appropriate side
- Equalise electrons transferred — multiply one or both half-reactions by suitable factors so electrons cancel
- Add both half-reactions; cancel identical species on both sides
- Check that all atoms and charges are balanced
For Basic Medium (Ion Electron Method):
After balancing in acidic conditions:
- Add OH⁻ ions to both sides equal to the number of H⁺ ions
- H⁺ + OH⁻ → H₂O (combine)
- Eliminate H₂O molecules appearing on both sides
- Final check: all elements and charges must balance
| Type | Electrolytic Cell | Galvanic (Voltaic) Cell |
|---|---|---|
| Energy conversion | Electrical → Chemical | Chemical → Electrical |
| Nature of reaction | Non-spontaneous | Spontaneous |
| Anode | Positive | Negative |
| Cathode | Negative | Positive |
| Electron flow | Cathode → Anode | Anode → Cathode |
| Salt bridge | Not required | Required |
Electrolysis of NaCl
1. Molten NaCl:
-
Oxidation: Cl⁻ → Cl₂ (gas)
-
Reduction: Na⁺ → Na (metal)
-
Products: Na (cathode), Cl₂ (anode)
2. Aqueous NaCl:
-
Oxidation: Cl⁻ → Cl₂
-
Reduction: H₂O → H₂ + OH⁻
-
Products: H₂ (cathode), Cl₂ (anode), NaOH formed
The Nernst equation is used to calculate the electrode or cell potential under non-standard conditions.
\[E_{cell}=E_{cell}^\circ-\frac{RT}{nF}\ln Q\]
At 25°C, it becomes:
\[E_{cell}=E_{cell}^\circ-\frac{0.0591}{n}\log Q\]
Where E°cell is the standard cell potential, n is the number of electrons transferred, and Q is the reaction quotient.
The equation helps determine the direction and spontaneity of a reaction:
- Ecell > 0 → spontaneous
- Ecell = 0 → equilibrium (Q = K)
It also relates to Gibbs energy:
ΔG = −nFEcell
Thus, the Nernst equation is important for electrochemical calculations and equilibrium analysis.
Concepts [17]
- Concept of Redox Reactions
- Classical Idea of Redox Reactions - Oxidation and Reduction Reactions
- Metallic Conductors and Electrolytic Conductors
- Conductance of Electrolytic Solutions
- Redox Reactions in Terms of Electron Transfer Reactions - Introduction
- Redox Reactions in Terms of Electron Transfer Reactions - Competitive Electron Transfer Reactions
- Oxidation Number
- Types of Redox Reactions
- Balancing of Redox Reactions
- Redox Reactions as the Basis for Titrations
- Limitations of Concept of Oxidation Number
- Balancing of Redox Reactions
- Redox Reactions and Electrode Processes
- Kohlrausch's law
- Faraday's Laws of Electrolysis
- Electrochemical Cells
- Nernst Equation
