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NEB Class 12 Routine 2080-2081: Class 12 Routine

Class 12 Chemistry Syllabus, Grid, Model Questions (NEB)

Latest NEB Class 12 Chemistry Syllabus, Specification Grid, and Model Questions for the year 2080. Marks distribution, Formal Plan are also available

Class 12 Chemistry Syllabus, Specific Grid, Model Questions 2079

Welcome to our post on the Class 12 Chemistry specific grid, curriculum, syllabus, and model question for the Nepal Examination Board (NEB) board exam in 2080.

The NEB has recently updated the syllabus and curriculum for the Class 12 Chemistry course.

The syllabus covers various topics including inorganic, applied, physical and organic chemistry.

The specific grid for the exam includes a total of 11 multiple choice questions worth 11 marks, 8 short answer questions worth 40 marks, and 3 long answer questions worth 24 marks.


Table of Contents

Specification Grid - Class 12 Chemistry

The Nepal Examination Board (NEB) has released the specification grid for Class 12 Chemistry, which outlines the format and content of the exam.

Question Type Number of Questions Total Marks
Multiple Choice 11 * 1 11
Short Answer 8 * 5 40
Long Answer 3 * 8 24

Additionally, an appendix has been provided which contains additional information and resources that can aid in Your exam preparation is given as:


Specification Grid Class 12 Chemistry

Appendix Class 12 Chemistry for NEB 2079 and 2080


Syllabus, Curriculum - Class 12 Chemistry

It covers a wide range of topics, including inorganic, applied, physical, and organic chemistry, to help students prepare for the upcoming NEB board exam in 2079.

General and Physical Chemistry

Unit 1. Volumetric Analysis (8 hrs)

  • 1.1 Introduction to gravimetric analysis, volumetric analysis, and equivalent weight

  • 1.2 Relationship between equivalent weight, atomic weight, and valency

  • 1.3 Equivalent weight of compounds (acid, base, salt, oxidizing and reducing agents)

  • 1.4 Concentration of solution and its units in terms of Percentage, g/L, molarity, molality, normality, and formality, ppm and ppb

  • 1.5 Primary and secondary standard substances

  • 1.6 Law of equivalence and normality equation

  • 1.7 Titration and its types: Acid-base titration, redox titration ( related numerical problems)

 

Unit 2. Ionic Equilibrium (10 hrs)

Introduction to Acids and Bases

  • 2.1. Limitation of Arrhenius's concepts of acids and bases

  • 2.2 Bronsted –Lowry definition of acids and bases

  • 2.3 Relative strength of acids and bases

  • 2.4 Conjugate acid-base pairs

  • 2.5 Lewis's definition of acids and bases

  • 2.6 Ionization of weak electrolyte (Ostwald's dilution law)

  • 2.7 Ionic product of water(Kw)

  • 2.8 Dissociation constant of acid and base, (Ka& Kb)

  • 2.9 Concept of pKa and pKb

  • 2.10 pH value: pH of strong and weak acids, pH of strong and weak bases

  • 2.11 Solubility and solubility product principle

  • 2.12 Common Ion effect

  • 2.13 Application of solubility product principle and common ion effect in precipitation reactions

  • 2.14 Buffer solution and its application

  • 2.15 Indicators and selection of indicators in acid-base titration

  • 2.16 Types of salts: Acidic salts, basic salts, simple salts, complex salts (introduction and examples)

  • 2.17 Hydrolysis of salts

  • 2.17.1 Salts of strong acid and strong base

  • 2.17.2 Salts of a weak acid and strong base

  • 2.17.3 Salts of a weak base and strong acid (solving related numerical problems)

 

Unit 3. Chemical kinetics (7 hrs)

  • 3.1 Introduction

  • 3.2 Rate of reactions: Average and instantaneous rate of reactions

  • 3.3 Rate law and its expressions

  • 3.4 Rate constant and it's unit and significance

  • 3.5 Order and molecularity

  • 3.6 Integrated rate equation for zero and first-order reaction

  • 3.7 Half-life of zero and first-order reactions

  • 3.8 Collision theory, the concept of activation energy and activated complex

  • 3.9 Factors affecting the rate of reactions: Effect of concentration, temperature (Arrhenius Equation), and effect of catalyst (energy profile diagram)

  • 3.10 Catalysis and types of catalysis: homogeneous, heterogeneous, and enzyme catalysis (solving related numerical problems based on rate, rate constant, and order of zero and first-order reactions)

 

Unit 4. Thermodynamics (8 hrs)

  • 4.1 Introduction

  • 4.2 Energy in chemical reactions

  • 4.3 Internal energy

  • 4.4 First law of thermodynamics

  • 4.5 Enthalpy and enthalpy changes: Endothermic and exothermic processes)

  • 4.6 Enthalpy of reaction, enthalpy of solution, enthalpy of formation, enthalpy of combustion

  • 4.7 Laws of thermochemistry (Laplace's Law and Hess’s law)

  • 4.8 Entropy and spontaneity

  • 4.9 Second law of thermodynamics

  • 4.10 Gibbs' free energy and prediction of spontaneity

  • 4.11 Relationship between ∆G and equilibrium constant (Solving related numerical problems)

 

Unit 5. Electrochemistry (7 hrs)

  • 5.1 Electrode potential and standard electrode potential

  • 5.2 Types of electrodes: Standard hydrogen electrodes and calomel electrodes

  • 5.3 Electrochemical series and its applications

  • 5.4 Voltaic cell: Zn-Cu cell, Ag- Cu cell

  • 5.5 Cell potential and standard cell potential

  • 5.6 Relationship between cell potential and free energy

  • 5.7 Commercial batteries and fuel cells (hydrogen/oxygen)

 

Inorganic chemistry

Unit 6. Transition metals (5 hrs)

  • 6.1 Introduction

  • 6.1.1 Characteristics of transition metals

  • 6.1.2 Oxidation states of transition metals

  • 6.1.3 Complex ions and metal complexes

  • 6.1.4 Shapes of complex ions

  • 6.1.5 d-orbitals in complex ions (simple explanation by crystal field theory) for octahedral complex

  • 6.1.6 Reasons for the color of transition metal compounds

  • 6.1.7 Catalytic properties of transition metals

 

Unit 7. Studies of heavy metals (15 hrs)

  • 7.1 Copper

  • 7.1.1 Occurrence and extraction of copper from copper pyrite

  • 7.1.2 Properties (with air, acids, aqueous ammonia, and metal ions) and uses of copper

  • 7.1.3 Chemistry (preparation, properties, and uses) of blue vitriol 

  • 7.1.4 Other compounds of copper (red oxide and black oxide of copper) formula and uses only

  • 7.2 Zinc

  • 7.2.1 Occurrence and extraction of zinc from zinc blende

  • 7.2.2 Properties (with air, acid, alkali, displacement reaction) and uses of zinc

  • 7.2.3 Chemistry (preparation, properties, and uses) of white vitriol

  • 7.3 Mercury

  • 7.3.1 Occurrence and extraction of mercury from cinnabar

  • 7.3.2 Properties of mercury

  • 7.3.3 Chemistry (preparation, properties, and uses) of calomel and corrosive sublimate

  • 7.4 Iron

  • 7.4.1 Occurrence and extraction of iron

  • 7.4.2 Properties and uses of iron

  • 7.4.3 Manufacture of steel by Basic Oxygen Method and Open Hearth Process

  • 7.4.4 Corrosion of iron and its prevention

  • 7.5 silver

  • 7.5.1 Occurrence and extraction of silver by cyanide process

  • 7.5.2 Preparation and uses of silver chloride and silver nitrate

 

Organic chemistry


Unit 8. Haloalkanes (8 hrs)

  • 8.1 Introduction

  • 8.2 Nomenclature, isomerism, and classification of monohaloalkanes

  • 8.3 Preparation of mono-haloalkanes from alkanes, alkenes, and alcohols

  • 8.4 Physical properties of monohaloalkanes

  • 8.5 Chemical properties, substitution reactions SN1 and SN2 reactions (basic concept only)

  • 8.6 Formation of alcohol, nitrile, amine, ether, thioether, carbylamines, nitrite, and nitro alkane using haloalkanes

  • 8.7 Elimination reaction (dehydrohalogenation- Saytzeff's rule), Reduction reactions, Wurtz reaction

  • 8.8 Preparation of trichloromethane from ethanol and propanone

  • 8.9 Chemical properties of trichloromethane: oxidation, reduction, action on silver powder, conc. nitric acid, propanone, and aqueous alkali

 

Unit 9. Haloarenes (3 hrs)

  • 9.1 Introduction

  • 9.2 Nomenclature and isomerism of haloarenes

  • 9.3 Preparation of chlorobenzene from benzene and benzene diazonium chloride

  • 9.4 Physical properties

  • 9.5 Chemical properties

  • 9.5.1 Low reactivity of haloarenes as compared to haloalkanes in terms of nucleophilic substitution reaction

  • 9.5.2 Reduction of chlorobenzene

  • 9.5.3 Electrophilic substitution reactions

  • 9.5.4 Action with Na (Fittig and Wurtz- Fittig reaction)

  • 9.5.5 Action with chloral

  • 9.6 Uses of haloarenes

 

Unit 10. Alcohols (7 hrs)

  • 10.1 Introduction

  • 10.2 Nomenclature, isomerism, and classification of monohydric alcohol

  • 10.3 Distinction of primary, secondary and tertiary alcohols by Victor Meyer's Method

  • 10.4 Preparation of monohydric alcohols from Haloalkane, primary amines, and esters

  • 10.5 Industrial preparation alcohol from oxo process, hydroboration-oxidation of ethene & fermentation of sugar

  • 10.6 Definition of common terms: Absolute alcohol, power alcohol, denatured alcohol (methylated spirit), rectified spirit; alcoholic beverage

  • 10.7 Physical properties of monohydric alcohols

  • 10.8 Chemical properties of monohydric alcohols

  • 10.8.1 Reaction with HX, PX3, PCl5, SOCl2

  • 10.8.2 Action with reactive metals like Na, K, Li

  • 10.8.3 Dehydration of alcohols

  • 10.8.4 Oxidation of primary, secondary, and tertiary alcohol with mild oxidizing agents like acidified KMnO4 or K2Cr2O7

  • 10.8.5 Catalyic dehydrogenation of 1° and 2°alcohol and dehydration of 3°alcohol

  • 10.8.6 Esterification reaction

  • 10.8.7 Test of ethanol

 

Unit 11. Phenols (4 hrs)

  • 11.1 Introduction and nomenclature

  • 11.2 Preparation of phenol from i. chlorobenzene ii. Diazonium salt and iii. benzene sulphonic acid

  • 11.3 Physical properties of phenol

  • 11.4 Chemical properties

  • 11.4.1 Acidic nature of phenol (comparison with alcohol and water)

  • 11.4.2 Action with NH3, Zn, Na, benzene diazonium chloride and phthalic anhydride

  • 11.4.3 Acylation reaction, Kolbe's reaction, Reimer-Tiemann's reaction

  • 11.4.4 Electrophilic substitution: nitration, sulphonation, bromination, and Friedel-Craft's alkylation

  • 11.5 Test of phenol: (FeCl3 test, aq. Bromine test & Libermann test)

  • 11.6 Uses of phenol

 

Unit 12. Ethers (2 hrs)

  • 12.1 Introduction

  • 12.2 Nomenclature, classification, and isomerism of ethers

  • 12.3 Preparation of aliphatic and aromatic ethers from Williamson's synthesis

  • 12.4 Physical properties of ether

  • 12.5 Chemical properties of ethoxyethane: action with HI, Conc. HCl, Conc. H2SO4, air and Cl2

  • 12.6 Uses of ethers

 

Unit 13. Aldehydes and ketones (10 hrs)

  • 13.1 Aliphatic aldehydes and ketones

  • 13.1.1 Introduction, nomenclature, and isomerism

  • 13.1.2 Preparation of aldehydes and ketones from Dehydrogenation and oxidation of alcohol, Ozonolysis of alkenes, Acid chloride, Gem dihaloalkane, Catalytic hydration of alkynes

  • 13.1.3 Physical properties of aldehydes and ketones

  • 13.1.4 Chemical properties

  • 13.1.4.1 Structure and nature of carbonyl group

  • 13.1.4.2 Distinction between aldehyde and ketones by using 2,4- DNP reagent, Tollen's reagent, Fehling's solution

  • 13.1.4.3 Addition reaction: addition of H2, HCN and NaHSO3

  • 13.1.4.4 Action of aldehyde and ketone with ammonia derivatives; NH2OH, NH2-NH2, phenyl hydrazine, semicarbazide,

  • 13.1.4.5 Aldol condensation

  • 13.1.4.6 Cannizzaro's reaction

  • 13.1.4.7 Clemmensen's reduction

  • 13.1.4.8 Wolf-Kishner reduction

  • 13.1.4.9 Action with PCl5 and action with LiAlH4

  • 13.1.4.10 Action of methanal with ammonia and phenol

  • 13.1.5 Formalin and its uses

  • 13.2 Aromatic aldehydes and Ketones

  • 13.2.1 Preparation of benzaldehyde from toluene and acetophenone from benzene

  • 13.2.2 Properties of benzaldehyde

  • 13.2.2.1 Perkin condensation

  • 13.2.2.2 Benzoin condensation

  • 13.2.2.3 Cannizzaro's reaction

  • 13.2.2.4 Electrophilic substitution reaction

 

Unit 14. Carboxylic acid and its derivatives (9 hrs)

  • 14.1 Aliphatic and aromatic carboxylic acids

  • 14.1.1 Introduction, nomenclature, and isomerism

  • 14.1.2 Preparation of monocarboxylic acids from aldehydes, nitriles, dicarboxylic acid, sodium alkoxide, and trihaloalkanes

  • 14.1.3 Preparation of benzoic acid from alkyl benzene

  • 14.1.4 Physical properties of monocarboxylic acids

  • 14.1.5 Chemical properties: Action with alkalies, metal oxides, metal carbonates, metal bicarbonates, PCl3, LiAlH4, and dehydration of carboxylic acid

  • 14.1.6 Hell-Volhard-Zelinsky reaction

  • 14.1.7 Electrophilic substitution reaction of benzoic acid - bromination, nitration, and sulphonation)

  • 14.1.8 Effect of constituents on the acidic strength of carboxylic acid

  • 14.1.9 Abnormal behavior of methanoic acid

  • 14.2 Derivatives of Carboxylic acids (acid halides, amides, esters, and anhydrides)

  • 14.2.1 Preparation of acid derivatives from carboxylic acid

  • 14.2.2 Comparative physical properties of acid derivatives

  • 14.2.3 Comparative chemical properties of acid derivatives (hydrolysis, ammonolysis, amines (RNH2), alcoholysis, and reduction only)

  • 14.2.4 Claisen condensation

  • 14.2.5 Hofmann bromamide reaction

  • 14.2.6 Amphoteric nature of amide

  • 14.2.7 Relative reactivity of acid derivatives

 

Unit 15. Nitro compounds (3 hrs)

  • 15.1 Nitroalkanes

  • 15.1.1 Introduction, nomenclature, and isomerism

  • 15.1.2 Preparation from haloalkane and alkane

  • 15.1.3 Physical properties

  • 15.1.4 Chemical properties: Reduction

  • 15.2 Nitrobenzene

  • 15.2.1 Preparation from benzene

  • 15.2.2 Physical properties

  • 15.2.3 Chemical properties

  • 15.2.4 Reduction in different media

  • 15.2.5 Electrophilic substitution reactions (nitration, sulphonation & bromination)

  • 15.2.6 Uses of nitro-compounds

 

Unit 16. Amines (7 hrs)

  • 16.1 Aliphatic amines

  • 16.1.1 Introduction, nomenclature, classification, and isomerism

  • 16.1.2 Separation of primary, secondary, and tertiary amines by Hoffmann's method

  • 16.1.3 Preparation of primary amines from haloalkane, nitriles, nitroalkanes, and amides

  • 16.1.4 Physical properties

  • 16.1.5 Chemical properties: basicity of amines, comparative study of basic nature of 1°, 2°, and 3° amines

  • 16.1.6 Reaction of primary amines with chloroform, conc. HCl, R-X, RCOX, and nitrous acid (NaNO2 / HCl)

  • 16.1.7 Test of 1, 2, and 3 amines (nitrous acid test)

  • 16.2 Aromatic amine (Aniline)

  • 16.2.1 Preparation of aniline from nitrobenzene, phenol

  • 16.2.2 Physical properties

  • 16.2.3 Chemical properties: basicity of aniline, comparison of basic nature of aniline with aliphatic amines and ammonia, alkylation, acylation, diazotization, carbylamine and coupling reaction, electrophilic substitution: Nitration sulphonation and bromination

  • 16.2.4 Uses of aniline

 

Unit 17. Organometallic compounds (2 hrs)

  • 17.1 Introduction, general formula, and examples of organolithium, organocopper, and organocadmium compounds

  • 17.2 Nature of Metal-Carbon bond

  • 17.3 Grignard reagent

  • 17.3.1 Preparation (using haloalkane and haloarene)

  • 17.3.2 Reaction of the Grignard reagent with water, aldehydes, and ketones ( preparation of primary, secondary, and tertiary alcohols), carbon dioxide, HCN, RCN, ester, and acid chloride

 

Applied Chemistry


Unit 18. Chemistry in the service of mankind (4 hrs)

  • 18.1 Polymers

  • 18.1.1 Addition and condensation polymers

  • 18.1.2 Elastomers and fibers

  • 18.1.3 Natural and synthetic polymers

  • 18.1.4 Some synthetic polymers (polyethylene, PVC, Teflon, polystyrene, nylon, and Bakelite)

  • 18.2 Dyes

  • 18.2.1 Introduction

  • 18.2.2 Types of dyes based on structure and method of application

  • 18.3 Drugs

  • 18.3.1 Characteristics of drugs

  • 18.3.2 Natural and synthetic drugs

  • 18.3.3 Classification of some common drugs

  • 18.3.4 Habit-forming drugs and drug addiction

  • 18.4 Pesticides

  • 18.4.1 Introduction to insecticides, herbicides, and fungicides

 

Unit 19. Cement (4 hrs)

  • 19.1 Introduction

  • 19.2 Raw materials for cement production

  • 19.3 Main steps in cement production (crushing and grinding, strong heating, and final grinding)

  • 19.4 Types of cement- OPC and PPC

  • 19.5 Portland cement process with flow-sheet diagram

  • 19.6 Cement Industry in Nepal

 

Unit 20. Paper and pulp (3 hrs)

  • 20.1 Introduction

  • 20.2 Raw materials

  • 20.3 Sources of raw materials

  • 20.4 Stages in the production of paper

  • 20.5 Flow-sheet diagram for paper production

  • 20.6 Quality of paper

 

Unit 21. Nuclear chemistry and application of radioactivity (2 hrs)

  • 21.1 Natural and artificial radioactivity

  • 21.2 Units of radioactivity

  • 21.3 Nuclear reactions

  • 21.4 Nuclear fission and fusion reactions

  • 21.5 Nuclear power and nuclear weapons

  • 21.6 Industrial uses of radioactivity

  • 21.7 Medical uses of radioactivity

  • 21.8 Radiocarbon dating

  • 21.9 Harmful effects of nuclear radiation

 


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Download Syllabus Class 11 and Class 12 Chemistry




Model Question - Class 12 Chemistry

The model question for Class 12 Chemistry for the 2079 Nepal Examination Board (NEB) board exam is an essential tool for students preparing for the exam. This can help students to become familiar with the format and structure of the exam.

This can include inorganic chemistry, applied chemistry, physical chemistry, and organic chemistry, as well as topics such as chemical reactions, thermochemistry, kinetics, and equilibrium including multiple choice questions, short answer questions, and long answer questions.

Class 12 Chemistry Model Question for NEB Exam 2079 is given as:

Class 12 Chemistry Model Question 2079
Class 12 Chemistry Model Question 2079
class 12 chemistry model question 2079
Class 12 Chemistry Model Question 2079
Class 12 Chemistry Model Question 2079
Class 12 Chemistry Model Question 2079 for NEB Exam

Download Model Question Class 12 Chemistry




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Iswori Rimal is the author of iswori.com.np, a popular education platform in Nepal. Iswori helps students in their SEE, Class 11 and Class 12 studies with Complete Notes, important questions and other study materials.

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