Electrolysis-Definition, Process, Applications, Electrolysis of Water

What Is Electrolysis?

Electrolysis is defined as a process of decomposing ionic compounds into their elements by passing a direct electric current through the compound in a fluid form. The cations are reduced at the cathode, and anions are oxidized at the anode. The main components that are required to conduct electrolysis are an electrolyte, electrodes, and some form of external power source is also needed. Additionally, a partition, such as an ion-exchange membrane or a salt bridge, is also used, but this is optional. They are used mainly to keep the products from diffusing near the opposite electrode.

An acidified or salt-containing water can be decomposed by passing an electric current to its original elements, hydrogen and oxygen. Molten sodium chloride can be decomposed into sodium and chlorine atoms.

Electrolysis was first popularised in the 19th century by Michael Faraday. It is a process that helped in the study of chemical reactions in obtaining pure elements. Today, electrolysis is commercially important as it is used widely in separating or obtaining pure elements from naturally occurring sources such as ores.

Electrolysis is usually done in a vessel named ‘electrolytic cell’ containing two electrodes (cathode and anode), connected to a direct current source and an electrolyte which is an ionic compound undergoing decomposition, in either molten form or in a dissolves state in a suitable solvent. Generally, electrodes that are made from metal, graphite and semiconductor materials are used. However, the choice of a suitable electrode is done based on the chemical reactivity between the electrode and electrolyte as well as the manufacturing cost.

Electrolytic Process

In the process of electrolysis, there is an interchange of ions and atoms due to the addition or removal of electrons from the external circuit. Basically, on passing current, cations move to the cathode, take electrons from the cathode (given by the supply source battery), and are discharged into the neutral atom. The neutral atom, if solid, is deposited on the cathode and, if gas, moves upwards. This is a reduction process, and the cation is reduced at the cathode.

At the same time, anions give up their extra electrons to the anode and are oxidized to neutral atoms at the anode. Electrons released by the anions travel across the electrical circuit and reach the cathode completing the circuit. Electrolysis involves a simultaneous oxidation reaction at the anode and a reduction reaction at the cathode.

For example, when an electric current is passed through molten sodium chloride, the sodium ion is attracted by the cathode, from which it takes an electrode and becomes a sodium atom.

Chloride ion reaches the anode, gives its electron, and becomes chlorine atoms to form chlorine molecules.

Na+(in electrolyte) + e(from cathode) → Na …. At Cathode

Cl(from electrolyte) → e + Cl → Cl2 …. At Anode

The electrolysis process, while useful to get elemental forms from compounds directly, can also be used indirectly in the metallurgy of alkali and alkaline earth metals, purification of metals, deposition of metals, preparation of compounds, etc.

Cell Potential or Voltage

The minimum potential needed for the electrolysis process depends on the ability of the individual ions to absorb or release electrons. It is also sometimes described as decomposition potential or decomposition voltage which is the minimum voltage (difference in electrode potential) between the anode and cathode of an electrolytic cell that enables electrolysis to occur.

The voltage at which electrolysis is thermodynamically preferred is the difference of the electrode potentials, as calculated using the Nernst equation. Applying additional voltage, referred to as overpotential, can increase the rate of reaction and is often needed above the thermodynamic value. It is especially necessary for electrolysis reactions involving gases such as oxygen, hydrogen or chlorine.

This ability is measured as an electrode potential of the ions present in the electrolytic cell. The cell potential is the sum of the potential required for the reduction and oxidation reaction. The potential involved in various redox reactions is available in literature as standard reduction potential.

Reaction with positive redox cell potentials will only be feasible as per thermodynamic Gibbs free energy (or standard potential). Generally, the electrolysis is thermodynamically controlled.

In electrolysis, a potential equal to or slightly more than that is applied externally. The ions, which are stable and not reacting, are made to undergo reaction in the presence of externally applied potential. External potential, hence, causes an unfavourable reaction to take place. In electrolysis, chemical bonds connecting atoms are either made or broken; hence, electrolysis involves the conversion of electrical energy into chemical energy.

Faraday’s Law of Electrolysis

The amount of the redox reaction depends on the quantity of electricity flowing through the cell. The amount of reaction or the number of ions discharged is given by Faraday’s law of electrolysis. There are two laws: Faraday’s first law and second law.

Faraday’s first law can be summarised as follows:

\(\begin{array}{l}m=\frac{EQ}{96485}=\frac{EIt}{96485}\end{array} \)

. Here, m is the mass of the substance that has undergone change, E is the equivalent mass of the substance, ‘I’ is the current and ”t is the time in seconds of the passing of current.

Faraday’s second law compares the mass of different substances undergoing a change for the same current.

According to the second law,

\(\begin{array}{l}\frac{M_1}{M_2}=\frac{E_1}{E_2}\,\,\,\ or\,\,\,\, \frac{M_1}{M_2}=\frac{M_1}{E_2}\end{array} \)

Here, M and E are the changed mass and equivalent mass of the substances, respectively.

Product of Electrolysis

The products of electrolysis reactions depend on the oxidising and reducing species present in the electrolytic cell. Electrolysis will produce products present in the compound. When more than one cation and anions are present, each ion will compete for reduction and oxidations. Reactions with more positive redox potentials will be reduced or oxidized in preference to others.

So, in spite of multiple redox couples present, only one can be reduced or oxidized. Sometimes, the ions that are reduced or oxidized may depend on their relative amount. In other words, the redox reaction and electrolysis may become kinetically controlled. In such cases, the product of analysis may differ on the relative concentration of the various ions present in the electrolyte.

For example, electrolysis of aqueous sodium chloride may give different products:

  1. Hydrogen and chlorine
  2. Hydrogen and oxygen
  3. Hydrogen, oxygen and chlorine.

Factors Affecting Electrolysis

The factors that may affect electrolysis are listed below:

i) The nature of the electrode

ii) Nature and state of the electrolyte

iii) Nature and electrode potential of ions present in the electrolyte

iv) Overvoltage at the electrodes.

i) Nature and State of the Electrolyte

Electrolysis involves the movement of ions towards the oppositely charged electrodes. Naturally, the electrolyte should have mobile ions. In solids, ions are in specific positions and cannot move at ordinary temperatures. Hence, solids are unsuitable for electrolysis.

For electrolysis, electrolytes should be in the liquid form – molten or in solution with a suitable polar solvent. Sodium chloride will undergo electrolysis in the molten state or in an aqueous solution.

ii) Nature and Electrode Potential of Ions Present in the Electrolyte

  • Electrolysis of electrolytes of two elemental ions is straightforward, giving the two elements on electrolysis. Molten sodium chloride gives sodium atoms and chlorine molecules.
  • Electrolysis of radical ions does not give the elemental atoms.
  • Electrolytes containing more than one ionic compound depend on the relative redox potentials.
  • Electrolysis of aqueous solutions of electrolytes – Water molecules also can undergo redox reactions and will compete with redox reactions of the electrolyte ions.
  • Electrolysis of molten sodium chloride gives sodium and chlorine. But, electrolysis of aqueous sodium chloride gives hydrogen and chlorine, and not sodium.

iii) Nature of the Electrode

For the same electrolyte, the nature of the electrolyte may give different products. When aqueous copper sulphate solution is, electrolyzed, the following redox reactions are possible.

At cathode: Reduction at pH =7

Cu2+ (aq) + 2e →Cu (s) E° = 0.34V and 2H2O + 2e→H2 + 2OH E° = -1.02V

At anode: Oxidation at pH = 7

Cu(s) →Cu2+ (aq) + 2e E° = – 0.34V and 2H2O → O2(g) + 4H+ + 4e E° = +1.4 V

At the cathode, out of the two electrodes, the reduction potential of copper ions is more positive than the reduction of water. So, irrespective of the electrode, copper ions from the electrolyte will be reduced and deposited on the cathode, increasing its mass. But, the reaction at the anode depends on the electrode.

Electrolysis with inert electrodes like platinum, graphite, etc. – Inert electrodes do not react with the electrolyte or the products, so does not undergo any changes. Since the oxidation of water has more positive potential, oxygen will be evolved at the anode.

But, if the copper is used as an anode, it will react with the sulphate ion to retain the electrolyte concentration. So, there will not be any gas evolution; instead, the anode mass slowly decreases, going into the solution.

iv) Overvoltage at the Electrodes

The redox potential of electrolyte ions decides the electrolysis reactions and products. Sometimes, the redox potentials of some half-reactions during the electrolysis are more than the thermodynamic potentials. This excess voltage (over-voltage) of the half-reaction may make the reaction unfavourable and change the product of electrolysis.

In the hydrolysis of aqueous sodium chloride at the anode, two oxidation reactions can take place. The reduction potential of water and chloride is +0.82V and 0.1.36V, respectively.

2H2O→O2(g) + 4H+ + 4e E° = -0.82 V

2Cl→ Cl2 + 2e E = – 1.36V

Oxidation of water being more positive is more feasible, so the evolution of oxygen gas should happen at the anode. But, the evolution of oxygen from water has an overvoltage of -0.6V, making the voltage for the oxidation of water as -1.42V. Chloride oxidation is more positive than the net voltage of water oxidation. Chloride is oxidized to chlorine at the anode. Chlorine is liberated, and not oxygen, because of overvoltage.

Electrolysis Applications

Electrolysis, as stated above, is a process of converting the ions of a compound in a liquid state into their reduced or oxidized state by passing an electric current through the compound. Thus, electrolysis finds many applications, both in experimental and industrial products. Some of the important ones are given below:

1) Determination of equivalent weight of substances.
2) Metallurgy of alkali and alkaline earth metals.
3) Purification of metals.
4) Manufacture of pure gases.
5) Manufacture of compounds like sodium hydroxide, sodium carbonate, potassium chlorate etc.
6) Electroplating for corrosion resistance, ornaments etc.

We will discuss the different applications of electrolysis in detail below.

Determination of Equivalent Weight of Substances

We know Faraday’s second law states that the mass of substances deposited is proportional to their equivalent weight. The mass of any deposited substance can be, mathematically related as:

\(\begin{array}{l}\frac{M_1}{E_1} = \frac{M_2}{E_2}\end{array} \)

The equivalent mass of an unknown metal or substance can be calculated by passing a known current through the solutions and determining the mass of substances (M1 and M2) deposited in their respective cells. If the equivalent mass of one substance is known, the equivalent mass of the unknown substance can be calculated from the above equation.

Electrolysis of Molten Salts

Metallurgy of alkali and alkaline earth and third group metals ores of metal is concentrated and converted mostly to oxides. Oxides are reduced with reducing agents such as carbon, aluminium etc. Since alkali and alkali earth metals have the largest reduction potentials, any other metals or their compounds cannot reduce them.

The only way of isolation of alkali and alkali earth metals is to directly electrolyze their molten chlorides. Mixing with other halides, like calcium chlorides, reduces the melting point of pure halides.

Electrorefining – Purification of Metals

Metals obtained after concentration and reduction of ores have a purity of about 90-99%. An aqueous solution of the metal salt with the impure metal as the anode and the pure metal as the cathode is electrolyzed. The pure metal of more than 99% purity deposits on the cathode, and the impurities are collected at the bottom as mud. Copper and nickel are some examples of the metal purified by electrorefining.

Electroplating

An object can be coated to the required thickness with a select metal by electrolysis. The object to be coated is made of the cathode. An aqueous solution of the metal salt to be coated is the electrolyte. The same metal or any inert metal can be the anode. In electrolysis, metal ion from the electrolyte deposit on the object. The loss of metal ions in the solution will be compensated if the same metal made the anode.

The deposition can be used to protect the metal from corrosion for making ornaments, etc. Coating iron with metals like zinc, lead, chromium, and nickel improves the corrosion resistance of iron. Gold and silver coating on cheaper metals is used for making ornaments.

It is also used in electrochemical machining (ECM). Here, an electrolytic cathode is used as a shaped tool for removing material by anodic oxidation from a workpiece. ECM technique is often used for deburring or for putting a permanent mark or logo on metal surfaces like tools or knives.

Electro-forming

Electroforming is a process of making a replica of objects using electrolysis. The object to be replicated is pressed in wax to make a mould. Graphite powder is coated uniformly to make it conductive. This is used as a cathode, and the salt of the metal to be deposited is taken as the electrolyte. After getting the required coating by electrolysis, the wax and the graphite are melted away.

Manufacture of Pure Gases

Aqueous salts on hydrolysis yield different products depending on the relative concentrations of salt and water. Electrolysis of concentrated brine (sodium chloride) forms pure hydrogen and chlorine gases. Pure chlorine gas is collected in the Chlor-alkali industries by the electrolysis of brine aqueous solution.

Pure hydrogen and oxygen are obtained by hydrolysis of water in the presence of acid or base or inert salt of alkali and alkaline earth metals. The percentage of hydrogen for commercial use is manufactured by the electrolysis of water worldwide.

Continuous electrolysis of water removes all the normal hydrogen isotopes leaving the deuterium ions. The deuterium oxide leftover after electrolysis of normal water is ‘heavy water’. Heavy water is used as a moderator in nuclear reactors producing electrical energy from nuclear reactions.

Manufacture of Compounds

Compounds like sodium hydroxide, sodium hydrosulphite, potassium permanganate, potassium chlorate, ammonium per-sulphate, heavy water etc., are manufactured by electrolysis. Sodium hydroxide is a side product in the chloralkali industries, preparing chlorine gas by the electrolysis of brine.

Potassium permanganate is obtained by the electrolysis of potassium manganite solution. Ammonium sulphate or ammonium bisulphate on electrolysis forms ammonium persulphate.

Electrocrystallization

This is a specialised application of electrolysis. In this process, conductive crystals are grown on one of the electrodes from oxidized or reduced species that are generated in situ. This technique is popularly used to manufacture single crystals of low-dimensional electrical conductors, such as linear chain compounds or charge-transfer salts.

Electrolysis Problems with Solutions

1. An iron pipe with a 14 cm diameter and length of 1 metre is to be galvanized to a thickness of 0.01 cm using zinc nitrate solution and a current of 25 amp. What will be the loss of mass from the zinc anode, and what will be the time required for the electrolysis? The density of zinc is 7.14g/cm3. The equivalent weight of zinc is 32.8

Volume of the zinc coating = 2πrxl × 0.01 cm3

Mass of the zinc to be coated= V × d

\(\begin{array}{l}=2\times\frac{22}{7}\times\frac{14}{2}\times1000\times0.01\end{array} \)

= 440g

The mass of the zinc lost from the anode = 440g.

By Faraday’s first law of electrolysis,

\(\begin{array}{l}m =\frac{EQ}{96485}=\frac{EIt}{96485}\,or\,t= \frac{96485\times m}{E\times l}=\frac{ 96485 \times 440}{32.8\times 25}\end{array} \)

= 51772sec

= 14.4hrs

2. A current of 3 amperes is passed through neutral water containing a small amount of sodium sulphate for one hour. Calculate the amount of hydrogen liberated at one atmosphere.

Number of coulombs passed = 3 × 60 × 60

Half reactions of the hydrolysis of water are –

At cathode: 2H2O + 2e → H2(g) + 2OH

At anode: 2H2O → O2(g) + 4H+ + 4e

The net reaction of electrolysis of water is, 2H2O → 2H2(g) + O2(g)

Four faradays or 4 x 96485 coulomb of electric current liberates 2 moles or 2× 22.4L of hydrogen gas.

10800 coulombs of electric current liberates hydrogen

\(\begin{array}{l}=\frac{2\times22.4\times10800}{4\times96485}\end{array} \)

= 1.25L

Total pressure above water = pressure of water vapour + pressure of hydrogen

The pressure of hydrogen = Total pressure above water – pressure of water vapour

The pressure of hydrogen = 1atm – 0.0316atm =0.9684atm

So, volume of hydrogen liberated 

\(\begin{array}{l}=\frac{1.25}{0.968}\end{array} \)

= 1.29L

Frequently Asked Questions on Electrolysis

Q1

What is electrolysis?

Electrolysis is a chemical reaction that occurs when an electric current is passed through a substance. The substance receives or loses an electron during a chemical reaction.

Q2

What is an electrolytic cell?

A positive and a negative electrode are kept apart and dipped into a solution containing positively and negatively charged ions in an electrolytic cell.

Q3

Where is the process of electrolysis used?

The process of electrolysis is widely used in metallurgical processes, including metal extraction and purification from other compounds and electroplating. Electrolysis of molten sodium chloride produces metallic sodium and chlorine gas. The electrolysis of water produces hydrogen and oxygen.

Er. Neeraj K.Anand is a freelance mentor and writer who specializes in Engineering & Science subjects. Neeraj Anand received a B.Tech degree in Electronics and Communication Engineering from N.I.T Warangal & M.Tech Post Graduation from IETE, New Delhi. He has over 30 years of teaching experience and serves as the Head of Department of ANAND CLASSES. He concentrated all his energy and experiences in academics and subsequently grew up as one of the best mentors in the country for students aspiring for success in competitive examinations. In parallel, he started a Technical Publication "ANAND TECHNICAL PUBLISHERS" in 2002 and Educational Newspaper "NATIONAL EDUCATION NEWS" in 2014 at Jalandhar. Now he is a Director of leading publication "ANAND TECHNICAL PUBLISHERS", "ANAND CLASSES" and "NATIONAL EDUCATION NEWS". He has published more than hundred books in the field of Physics, Mathematics, Computers and Information Technology. Besides this he has written many books to help students prepare for IIT-JEE and AIPMT entrance exams. He is an executive member of the IEEE (Institute of Electrical & Electronics Engineers. USA) and honorary member of many Indian scientific societies such as Institution of Electronics & Telecommunication Engineers, Aeronautical Society of India, Bioinformatics Institute of India, Institution of Engineers. He has got award from American Biographical Institute Board of International Research in the year 2005.

CBSE Class 12 Chemistry Syllabus Download PDF

Below is the CBSE Class 12 Syllabus along with the marking scheme and time duration of the Chemistry exam.

S.NoTitleNo. of PeriodsMarks
1Solutions107
2Electrochemistry129
3Chemical Kinetics107
4d -and f -Block Elements127
5Coordination Compounds127
6Haloalkanes and Haloarenes106
7Alcohols, Phenols and Ethers106
8Aldehydes, Ketones and Carboxylic Acids108
9Amines106
10Biomolecules127
Total70

CBSE Class 12 Chemistry Practical Syllabus along with Marking Scheme

The following is a breakdown of the marks for practical, project work, class records, and viva. The total number of marks for all parts is 15. The marks for both terms are provided in the table below.

Evaluation Scheme for ExaminationMarks
Volumetric Analysis08
Salt Analysis08
Content-Based Experiment06
Project Work and Viva04
Class record and Viva04
Total30

CBSE Class 12 Chemistry Syllabus (Chapter-wise)

Unit -1: Solutions

  • Raoult's law.
  • Colligative properties - relative lowering of vapour pressure, elevation of boiling point, depression of freezing point, osmotic pressure, determination of molecular masses using colligative properties, abnormal molecular mass.
  • Solutions, Types of solutions, expression of concentration of solutions of solids in liquids, solubility of gases in liquids, solid solutions.
  • Van't Hoff factor.

Unit -2: Electrochemistry

  • Redox reactions, EMF of a cell, standard electrode potential
  • Nernst equation and its application to chemical cells
  • Relation between Gibbs energy change and EMF of a cell
  • Kohlrausch's Law
  • Electrolysis and law of electrolysis (elementary idea)
  • Dry cell-electrolytic cells and Galvanic cells
  • Conductance in electrolytic solutions, specific and molar conductivity, variations of conductivity with concentration.
  • Lead accumulator
  • Fuel cells

Unit -3: Chemical Kinetics

  • Rate of a reaction (Average and instantaneous)
  • Rate law and specific rate constant
  • Integrated rate equations and half-life (only for zerfirst-order order reactions)
  • Concept of collision theory (elementary idea, no mathematical treatment)
  • Factors affecting rate of reaction: concentration, temperature, catalyst;
  • Order and molecularity of a reaction
  • Activation energy
  • Arrhenius equation

Unit -4: d and f Block Elements  

  • Lanthanoids- Electronic configuration, oxidation states, chemical reactivity and lanthanoid contraction and its consequences.
  • Actinoids- Electronic configuration, oxidation states and comparison with lanthanoids.
  • General introduction, electronic configuration, occurrence and characteristics of transition metals, general trends in properties of the first-row transition metals – metallic character, ionization enthalpy, oxidation states, ionic radii, color, catalytic property, magnetic properties, interstitial compounds, alloy formation, preparation and properties of K2Cr2O7 and KMnO4.

Unit -5: Coordination Compounds  

  • Coordination compounds - Introduction, ligands, coordination number, color, magnetic properties and shapes
  • The importance of coordination compounds (in qualitative analysis, extraction of metals and biological system).
  • IUPAC nomenclature of mononuclear coordination compounds.
  • Bonding
  • Werner's theory, VBT, and CFT; structure and stereoisomerism

Unit -6: Haloalkanes and Haloarenes  

  • Haloarenes: Nature of C–X bond, substitution reactions (Directive influence of halogen in monosubstituted compounds only). Uses and environmental effects of - dichloromethane, trichloro methane, tetrachloromethane, iodoform, freons, DDT.
  • Haloalkanes: Nomenclature, nature of C–X bond, physical and chemical properties, optical rotation mechanism of substitution reactions.

Unit -7: Alcohols, Phenols and Ethers   

  • Phenols: Nomenclature, methods of preparation, physical and chemical properties, acidic nature of phenol, electrophilic substitution reactions, uses of phenols.
  • Ethers: Nomenclature, methods of preparation, physical and chemical properties, uses.
  • Alcohols: Nomenclature, methods of preparation, physical and chemical properties (of primary alcohols only), identification of primary, secondary and tertiary alcohols, mechanism of dehydration, and uses with special reference to methanol and ethanol.

Unit -8: Aldehydes, Ketones and Carboxylic Acids   

  • Carboxylic Acids: Nomenclature, acidic nature, methods of preparation, physical and chemical properties; uses.
  • Aldehydes and Ketones: Nomenclature, nature of carbonyl group, methods of preparation, physical and chemical properties, mechanism of nucleophilic addition, the reactivity of alpha hydrogen in aldehydes, uses.

Unit -9: Amines    

  • Diazonium salts: Preparation, chemical reactions and importance in synthetic organic chemistry.
  • Amines: Nomenclature, classification, structure, methods of preparation, physical and chemical properties, uses, and identification of primary, secondary and tertiary amines.

Unit -10: Biomolecules     

  • Proteins -Elementary idea of - amino acids, peptide bond, polypeptides, proteins, structure of proteins - primary, secondary, tertiary structure and quaternary structures (qualitative idea only), denaturation of proteins; enzymes. Hormones - Elementary idea excluding structure.
  • Vitamins - Classification and functions.
  • Carbohydrates - Classification (aldoses and ketoses), monosaccharides (glucose and fructose), D-L configuration oligosaccharides (sucrose, lactose, maltose), polysaccharides (starch, cellulose, glycogen); Importance of carbohydrates.
  • Nucleic Acids: DNA and RNA.

The syllabus is divided into three parts: Part A, Part B, and Part C. Part A consist of Basic Concepts of Chemistry, which covers topics such as atomic structure, chemical bonding, states of matter, and thermochemistry. Part B consists of Topics in Physical Chemistry, which includes topics such as chemical kinetics, equilibrium, and electrochemistry. Part C consists of Topics in Organic Chemistry, which covers topics such as alkanes, alkenes, alkynes, and aromatic compounds.

Basic Concepts of Chemistry:

  • Atomic structure: This section covers the fundamental concepts of atomic structure, including the electronic configuration of atoms, the Bohr model of the atom, and the wave nature of matter.
  • Chemical bonding: This section covers the different types of chemical bonds, including ionic, covalent, and metallic bonds, as well as the concept of hybridization.
  • States of the matter: This section covers the three states of matter - solid, liquid, and gas - and the factors that influence their properties.
  • Thermochemistry: This section covers the principles of thermochemistry, including the laws of thermodynamics and the concept of enthalpy.

Chapters in Physical Chemistry:

  • Chemical kinetics: This section covers the study of the rate of chemical reactions and the factors that influence it, including the concentration of reactants, temperature, and the presence of catalysts.
  • Equilibrium: This section covers the principles of chemical equilibrium, including the concept of Le Chatelier's principle and the equilibrium constant.
  • Electrochemistry: This section covers the principles of electrochemistry, including the concept of half-cell reactions, galvanic cells, and electrolysis.

Chapters in Organic Chemistry:

  • Alkanes: This section covers the properties and reactions of alkanes, including their structure, isomerism, and combustion.
  • Alkenes: This section covers the properties and reactions of alkenes, including their structure, isomerism, and addition reactions.
  • Alkynes: This section covers the properties and reactions of alkynes, including their structure, isomerism, and addition reactions.
  • Aromatic compounds: This section covers the properties and reactions of aromatic compounds, including their structure, isomerism, and electrophilic substitution reactions.

In addition to the topics covered in the syllabus, the CBSE Class 12 Chemistry exam also tests students on their analytical and problem-solving skills, as well as their ability to apply the concepts learned in the classroom to real-world situations.

Students can also check out the Tips for the Class 12 Chemistry Exam. They can easily access the Class 12 study material in one place by visiting the CBSE Class 12 page at ANAND CLASSES (A School Of Competitions). Moreover, to get interactive lessons and study videos, download the ANAND CLASSES (A School Of Competitions) App.

Frequently Asked Questions on CBSE Class 12 Chemistry Syllabus

Q1

How many chapters are there in the CBSE Class 12 Chemistry as per the syllabus?

There are 10 chapters in the CBSE Class 12 Chemistry as per Syllabus. Students can learn all these chapters efficiently using the study materials provided at ANAND CLASSES (A School Of Competitions).

Q2

What is the marking scheme for CBSE Class 12 Chemistry practical exam according to the syllabus?

The marking scheme for CBSE Class 12 Chemistry practical exam, according to the syllabus, is 8 marks for volumetric analysis, 8 marks for salt analysis, 6 marks for the content-based experiment, 4 marks for the project and viva and 4 marks for class record and viva.

Q3

Which is the scoring chapter in Chemistry as per CBSE Class 12 syllabus?

The chapter Electrochemistry in Chemistry is the scoring chapter as per CBSE Class 12 syllabus.