Chemistry Class 12 Electrochemistry Notes

chemistry 12 electrochemistry notes

This article is on the Electrochemistry Class 12 Notes of Chemistry. The notes on the electrochemistry of class 12 chemistry have been prepared with great care keeping in mind the effectiveness of it for the students. This article provides the revision notes of the electrochemistry chapter of Class 12 Chemistry for the students so that they can give a quick glance of the chapter.

The entire chapter of electrochemistry has been divided into two articles. This article (Part 2) is on Electrolysis, Batteries, Fuel Cells and Corrosion. The first article (Part 1) includes the Electrochemical cell, Electrolytic cell, Nernst equation, Conductance, Types of electrolytes and Kohlrausch Law.

ELECTROCHEMISTRY (PART 2)

Electrolysis:

In electrolytic cells, electrical energy is used to carry out non-spontaneous chemical reactions and the reaction which takes place in an electrolytic cell is called electrolysis.

Many metals such as Na Mg, Al are produced by electrochemical reduction of their respective cations on a large scale where no suitable chemical reducing agents are available for this purpose.

Faraday’s Law of Electrolysis:

The quantitative aspect of electrolysis was studied extensively by Michael Faraday and his laws of electrolysis are known as Faraday’s law of electrolysis.

Faraday’s First Law of Electrolysis:

The amount of chemical reaction which occurs at any electrode during electrolysis by a current is proportional to the quantity of electricity passed through the electrolyte, i.e., m = ZQ or ZIt, where, m is the mass of substance deposited, current ‘I’ is in ampere and t is the time in seconds.

Q = It

Z= Equivalent weight/96500

where Z is the electrochemical equivalent of the substance deposited.

[Charge on 1 electron= 1.602x 10-19 C, charge on 1 mole of electrons = 1.602x 10-19 x 6.023x 1023 = 96500 C]

Faraday’s Second Law of Electrolysis:

The amounts of different substances liberated by the same quantity of electricity passing through the electrolytic solution are proportional to their chemical equivalent weight w1/E1 = w2/E2 = w3/E3 ……. where w1 is the mass of substance 1 deposited and E1 is the equivalent weight and so on.

Products of Electrolysis:

It depend upon the nature of electrolyte being electrolysed and the nature of electrodes. If electrodes are inert like Pt or Au, they do not take part in chemical reaction. The products of electrolysis also depend upon the electrode potentials of oxidising and reducing species.

(i) Electrolysis of CuC12 @q) using Pt electrode,

CuCl2 (aq) —> Cu2+ (aq) + 2 Cl (aq)

At anode 2 Cl (aq) —> Cl2(g) + 2e

At cathode   Cu2+ (aq) + 2e —> Cu(s)

(ii) Electrolysis of CuCl2 using Cu electrode.

At anode Cu(S) —> Cu2+ (aq) + 2e

At cathode:  Cu2+(aq) + 2e —> Cu (s)

(iii) Electrolysis of AgNO3 (aq) using Pt electrode:

AgNO3 (aq) —> Ag+(aq) + NO3

At cathode Ag+ (aq) + e–  —> Ag (s)

At anode  2H20 (l) —> O2 (g) + 4H+ (aq) +4e

(iv) Electrolysis of AgNO3 using Ag electrode

At anode Ag (s)  —> Ag+ (aq) + e

At cathode  Ag+ (aq) + e–   —>  Ag (s)

Electrolysis of Molten and Aqueous Sodium Chloride:

If we use molten NaCl, the products of electrolysis are sodium metal and Cl2 gas. Here, we have only one cation [Na+ ] which is reduced at the cathode (Na+ + e—> Na) and one anion (Cl) which is oxidised at the anode (Cl—>1/2  Cl2 + e). During the electrolysis of aqueous sodium chloride solution, the products are NaOH, Cl2 and H2. In this case besides Na+ and Cl- ions, we also have H+ and OH ions along with the solvent molecules, H2O.

At the cathode, there is competition between the following reduction reactions:

Na+ (aq) + e —> Na (s)

H+ (aq) + e — ½ H2 (g)

The reaction with higher value of E° is preferred and therefore, the reaction at the cathode during electrolysis is

H+ (aq) + e — ½ H2 (g)

but H+ (aq) is produced by the dissociation of H2O, i.e.,

H20 (l) —> H+ (aq) + OH (aq)

Therefore, the net reaction at the cathode may be written as

H2O (l) + e —> ½ H2 (g)+ OH.

At the anode, the following oxidation reactions are possible

Cl (aq) –> ½  Cl2 (g) + e                                             E°cell =1.36 V

2H20 (l) —>  02 (g) + 4H+ (aq) + 4e                           E°cell  =1.23V

The reaction at anode with lower value of E° is preferred and therefore, water should get oxidised in preference to Cl (aq). However, on account of over potential of oxygen, oxidation of Cl ions is preferred. Thus, the net reactions may be summarised as

NaCl (aq) —> Na+ (aq) + Cl (aq)

Cathode H20 (l) + e —>  H2 (g) + OH(aq)

Anode Cl (aq) —>  ½  Cl2 (g) + e

Net reaction

NaCl(aq) + H2O (l) —> Na+ (aq) + OH (aq) + ½ H­2 (g) + Cl2 (g)

Batteries:

A battery or a cell that we use as a source of electrical energy is basically a galvanic cell where the chemical energy of the redox reaction is converted into electrical energy.

There are two types of batteries

  1. Primary Cell:

The cell in which products cannot be changed into reactants back is called a primary cell, e.g., Daniell cell, mercury cell.

Dry Cell (Leclanche Cell):

Dry Cell (Leclanche Cell)

It is also known as the primary voltaic cell and consists of a zinc container which acts as an anode and carbon (graphite) rod as a cathode surrounded by powdered manganese dioxide and carbon. A moist paste of NH4Cl and ZnCl2 is filled in between the electrodes space.

The reactions are

At anode Zn(s) —> Zn2+ +2e

At cathode MnO2 + NH4+ + e —>  MnO(OH) + NH3

Ammonia produced in the reaction forms a complex with Zn2+ to give [Zn(NH3)4]2+. The cell has a potential of nearly 1.5 V.

Mercury Cell:

chemistry 12 electrochemistry notes

It consists of Zn-Hg amalgam as an anode. The cathode is a paste of mercuric oxide (HgO) and carbon powder. The electrolyte is a paste of KOH and ZnO.

The electrodes reactions are given as

At anode Zn(Hg) + 2 OH–   —>  ZnO (s) + H20+ 2e

At cathode HgO+ H20+ 2e –> Hg(l) + 20H

The overall reaction is

Zn(Hg) + HgO(s) –> ZnO (s) + Hg(l)

The cell potential is approximately 1.35 V and remains constant during its life because the overall reaction does not involve any ion in solution whose concentration can change during its life time.

  1. Secondary Cell:

A secondary cell is capable of being charged after discharge again and again, e.g., lead storage battery, nickel-cadmium battery.

Lead Storage Battery:

Lead Storage Battery

It consists of a lead anode and a grid of lead packed with lead dioxide as the cathode. A solution of sulphuric acid acts as the electrolyte.

When the battery is in use (discharging), the cell reactions are

At anode Pb(s) + SO42- (aq) —>  PbSO4 (s)

At cathode Pb02 (s) + SO42- (aq) + 4H+ (aq) + 2e –> PbSO4 (s) + 2H2O (l)

The overall reaction is

Pb(s) + Pb02(s) + H2SO4 (aq) –> 2PbSO4 (s) + 2H2O (l)

During charging, the reactions are reversed.

Nickel-Cadmium Battery (Ni-Cd Cell):

chemistry 12 electrochemistry notes

It consists of a cadmium anode and metal grid containing Ni02 as the cathode. A solution of KOH acts as an electrolyte.

The overall cell reaction of Ni-Cd cell during discharging is

Cd(s) + 2Ni (OH)3 (s) –> CdO (s) + Ni(OH)2 (s) + 2H2O (l)

It has a longer life than the lead storage cell but more expensive to manufacture.

Fuel Cells:

These are the galvanic cells that convert the energy of combustion of fuels directly into electrical energy. Energy can be obtained indefinitely from the fuel cell as long as outside supply of fuel is maintained.

Hydrogen-Oxygen Fuel Cell:

Hydrogen-Oxygen Fuel Cell

In this fuel cell, H2 and 02 gases are bubbled through porous carbon electrodes into concentrated aqueous sodium hydroxide solution. Finely divided platinum or palladium acts as a catalyst.

The electrode reactions of H2 – 02 fuel cell are

At anode 2H2 (g) + 4OH (aq) —>  4H20 + 4e

At cathode 02 (g) + 2H2O(l) + 4e  —> 40H(aq)

The overall reaction is 2H2 (g) + 02 (g) —> 2 H20(l)

Efficiency of a cell = ∆G/∆H = Useful work/Total work

Fuel cells are pollution free, produce electricity with an efficiency of about 70%. It is also used as an primary source of electrical energy on the moon flights.

Corrosion:

corrosion

It is basically an electrochemical phenomenon in which a metal oxide or other salt of the metal forms a coating on the metal surface. The rusting of iron, tarnishing of silver surface, the surface of copper and bronze turning green are some of the examples of corrosion.

Rusting is an electrochemical phenomenon that occurs in the presence of water and air.

Oxidation: Fe(s) —> Fe2+(aq) + 2e

Reduction:  O2 (g) + 4H+ (aq) + 4e —>2H 2O (1)

The overall reaction is

2Fe (s) + 02 (g) + 4H+ (aq) —> 2 Fe2+ (aq) + 2 H20 (l)

Atmospheric oxidation (when Fe2+ ions are further oxidised by atmospheric oxygen).

2Fe2+ (aq) + 2H20 (1) + —1/2 02(g) —> Fe2O3 (s) + 4H+ (aq)

Prevention of Corrosion:

One of the simplest method of preventing corrosion is to prevent the metal surface to come in contact with the atmosphere. This can be done by barrier protection through coating of paints or electroplating. Another simple method is galvanization or coating of surface with tin metal. It can also be done by the use of anti-rust solutions.

The notes on electrochemistry (Part 1) for class 12 Chemistry has been given below.

Electrochemistry (Part 1): Electrochemical cell, Electrolytic cell, Nernst equation, Conductance, Types of electrolytes and Kohlrausch Law.

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