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SCIENCE (52)

CHEMISTRY

SCIENCE Paper - 2
Aims:
3. To acquire skills in proper handling of apparatus
1. To acquire the knowledge of terms, concepts, and chemicals.
processes, techniques and principles related to
4. To develop scientific temper, attitude and
the subject.
problem-solving skills.
2. To develop the ability to apply the knowledge of
5. To recognize Chemical Science as having an
contents and principles of chemistry in
important impact on the environment relating to
unfamiliar situations.
cycles in nature; natural resources, pollution.
CLASS IX

There will be one paper of two hours duration of (ii) Relative Atomic Masses (atomic weights)
80 marks and Internal Assessment of practical and Relative Molecular Masses (molecular
work carrying 20 marks. weights): either - standard H atom or 1/12th
of carbon 12 atom.
The paper will be divided into two sections,
Section I (40 marks) and Section II (40 marks). • Definitions
• Calculation of Relative Molecular
Section I (compulsory) will contain short answer Mass and percentage composition of a
questions on the entire syllabus. compound.
Section II will contain six questions. Candidates
will be required to answer any four of these six 2. Chemical changes and reactions
questions. (i) Types of chemical changes.
Note: All chemical reactions should be studied • Direct combination
with reference to the reactants, products, • Decomposition
conditions, observations and the (balanced) • Displacement;
equations. • Double decomposition
1. The Language of Chemistry (The above to be taught with suitable
chemical equations as examples).
(i) Symbol of an element; valency; formulae
of radicals and formulae of compounds. (ii) Energy changes in a chemical change.
Balancing of simple chemical equations. Exothermic and endothermic reactions
• Symbol – definition; symbols of the with examples – evolution/absorption of
elements used often. heat, light and electricity.
• Valency - definition; hydrogen
combination and number of valence 3. Water
electrons of the metals and non- (i) Water as a universal solvent.
metals; mono, di, tri and tetra valent
elements. • Solutions as 'mixtures' of solids in
• Radicals – definition; formulae and water; saturated solutions.
valencies. • Qualitative effect of temperature
• Compounds – name and formulae. on solubility (e.g. solutions of
• Chemical equation – definition and calcium sulphate, potassium
examples of chemical equations with nitrate and sodium chloride in
one reactant and two or three water).
products, two reactants and one
product, two reactants and two (ii) Hydrated and anhydrous substances.
products and two reactants and three (a) Hydrated substances:
or four products; balancing of
equations. (by hit and trial method). Water of Crystallisation –
meaning and examples.
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(b) Anhydrous substances: 5. The Periodic Table
Meaning and examples only Dobereiner’s Triads, Newland’s law of
(c) Properties: Octaves, Mendeleev’s contributions; Modern
• Efflorescence Periodic Law, the Modern Periodic Table.
• Deliquescence (Groups and periods)
• Hygroscopy • General idea of Dobereiner’s triads,
Newland’s law of Octaves, Mendeleev’s
• Removal of hardness periodic law.
(i) By boiling • Discovery of Atomic Number and its use as
(ii) By addition of washing soda a basis for Modern Periodic law.
(Definition and examples of each of • Modern Periodic Table (Groups 1 to 18
the above). and periods 1 to 7).
(iii) Drying and Dehydrating Agents • Special reference to Alkali metals (Group
Meaning and examples only. 1), Alkaline Earth metals (Group 2)
(iv) Soft water and Hard water Halogens (Group 17) and Zero Group
(Group 18).
• Meaning, (in terms of action of
soap) 6. Study of the First Element -Hydrogen
• Advantages and disadvantages of
soft water and hard water. Position of the non-metal (Hydrogen) in the
periodic table and general group
• Types and causes of hardness. characteristics with reference to valency
electrons, burning, ion formation applied to the
4. Atomic Structure and Chemical bonding above-mentioned element.
(i) Structure of an Atom, mass number and (i) Hydrogen from: water, dilute acids and
atomic number, Isotopes and Octet Rule. alkalis.
• Definition of an atom (a) Hydrogen from water:
• Constituents of an atom - nucleus • The action of cold water on
(protons, neutrons) with associated sodium potassium and calcium.
electrons; mass number, atomic
• The action of hot water on
number. magnesium.
• Electron distribution in the orbits -
2n2 rule, Octet rule. Reason for • The action of steam on aluminium,
chemical activity of an atom. zinc, and iron; (reversibility of
• Definition and examples of isotopes reaction between iron and steam).
(hydrogen, carbon, chlorine). • The action of steam on non-metal
(ii) Electrovalent and covalent bonding, (carbon).
structures of various compounds – orbit Students can be shown the action
structure of sodium and calcium on water
(a) Electrovalent Bond in the laboratory. They must be
• Definition asked to make observations and
• Atomic orbit structure for the write equations for the above
formation of Electrovalent reactions.
compounds (e.g. NaCl, MgCl2, Application of activity series for
CaO); the above-mentioned reactions.
(b) Covalent Bond (b) Displacement of hydrogen from dilute
• Definition acids.
• Atomic orbit structure for the
formation of Covalent molecules The action of dilute sulphuric acid or
hydrochloric acid on metals: Mg, Al,
on the basis of duplet and octet of
Zn and Fe .
electrons (examples: hydrogen,
chlorine, oxygen, nitrogen, (To understand reasons for not using
hydrogen chloride, water, other metals and dilute nitric acid.)
ammonia, carbon tetrachloride,
methane.)

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(c) Displacement of hydrogen from alkalis. 8. Atmospheric pollution
The action of Alkalis ((NaOH, KOH) on (a) Acid rain – composition, cause and its
Al, Zn and Pb – unique nature of these impact.
elements.
Sulphur in fossil fuels giving oxides of
(ii) The preparation and collection of sulphur when burnt. High temperatures
hydrogen by a standard laboratory method in furnaces and internal combustion
other than electrolysis.
engines produce oxides of nitrogen.
In the laboratory preparation, the reason (Equations to be included). Acid rain
for using zinc, the impurities in the gas, affects soil chemistry and water bodies.
their removal and the precautions in the
collection of the gas must be mentioned. (b) Global warming:
Greenhouse gases – their sources and
(iii) Industrial manufacture of hydrogen by ways of reducing their presence in the
Bosch process.
atmosphere.
• Main reactions and conditions. (Water vapour, carbon dioxide, methane
• Separation of CO2 and CO from and oxides of nitrogen)
hydrogen.
(c) Ozone depletion
(iv) Oxidation and reduction reactions.
• Formation of ozone – relevant
Differences in terms of addition and equations
removal of oxygen / hydrogen. • Function in the atmosphere.
7. Study of Gas Laws • Destruction of the ozone layer –
chemicals responsible for this to be
(i) The behaviour of gases under changes of named but reactions not required.
temperature and pressure; explanation in
terms of molecular motion (particles,
INTERNAL ASSESSMENT OF
atoms, molecules); Boyle’s Law and
Charles’ Law; absolute zero; gas equation; PRACTICAL WORK
simple relevant calculations.
Candidates will be asked to observe the effect of
• The behaviour of gases under reagents and/or of heat on substances supplied to
changes of temperature and
pressure; explanation in terms of them. The exercises will be simple and may
molecular motion (particles, atoms, include the recognition and identification of certain
molecules). gases listed below.
• Boyle’s Law: statement, Gases: Hydrogen, Oxygen, Carbon dioxide,
mathematical form, simple
calculations. Chlorine, Hydrogen chloride, Sulphur dioxide,
Hydrogen sulphide, Ammonia, Water vapour,
• Charles’ Law: statement, Nitrogen dioxide.
mathematical form, simple
calculations. Candidates are expected to have completed the
• Absolute zero Kelvin scale of following minimum practical work.
temperature.
Simple experiments on:
• Gas equation P1 V1 / T1 = P2 V2 / T2;
simple relevant calculations based 1. Action of heat on the following compounds:
on gas equation. (a) copper carbonate, zinc carbonate
(ii) Relationship between Kelvin scale and (b) washing soda, copper sulphate crystals
Celsius Scale of temperature; Standard
(c) zinc nitrate, copper nitrate, lead nitrate
temperature and pressure.
Conversion of temperature from Celsius (d) ammonium chloride, iodine, ammonium
Scale to Kelvin scale and vice versa. dichromate
Standard temperature and pressure. Make observations, identify the products and
(Simple calculations). make deductions where possible.

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2. Action of dilute sulphuric acid on the 3. Apply the flame test to identify the metal in the
following substances. (warm if necessary) unknown substance.
(a) a metal (a) a sodium salt
(b) a carbonate (b) a potassium salt
(c) a sulphide (c) a calcium compound
(d) a sulphite
4. Simple experiments based on hard water and
Make observations, identify the gas evolved soft water – identification of hardness –
and make deductions. simple softening – by heating the temporary
hard water, using washing soda and
advantage of using detergents over soap in
hard water.
5. Find out the sources of pollution of water
bodies in the locality. Suggest preventive
steps to control it.

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CLASS X

There will be one paper of two hours duration of 2. Chemical Bonding


80 marks and Internal Assessment of practical work Electrovalent, covalent and co-ordinate
carrying 20 marks. bonding, structures of various compounds,
The paper will be divided into two sections, Electron dot structure.
Section I (40 marks) and Section II (40 marks). (a) Electrovalent bonding:
Section I (compulsory) will contain short answer • Electron dot structure of Electrovalent
questions on the entire syllabus. compounds NaCl, MgCl2, CaO.
Section II will contain six questions. Candidates • Characteristic properties of
will be required to answer any four of these six electrovalent compounds – state of
questions. existence, melting and boiling points,
conductivity (heat and electricity),
Note: All chemical process/reactions should be dissociation in solution and in molten
studied with reference to the reactants, products, state to be linked with electrolysis.
conditions, observation, the (balanced) equations (b) Covalent Bonding:
and diagrams.
• Electron dot structure of covalent
1. Periodic Properties and variations of molecules on the basis of duplet and
Properties – Physical and Chemical octet of electrons (example: hydrogen,
chlorine, nitrogen, ammonia, carbon
(i) Periodic properties and their variations in tetrachloride, methane.
groups and periods.
• Polar Covalent compounds – based on
Definitions and trends of the following difference in electronegativity:
periodic properties in groups and periods
Examples – HCl and H2O including
should be studied:
structures.
• atomic size
• Characteristic properties of Covalent
• metallic character compounds – state of existence, melting
• non-metallic character and boiling points, conductivity (heat
• ionisation potential and electricity), ionisation in solution.
Comparison of Electrovalent and
• electron affinity
Covalent compounds.
• electronegativity
(c) Coordinate Bonding:
(ii) Periodicity on the basis of atomic number for • Definition
elements.
• The lone pair effect of the oxygen atom
• The study of modern periodic table up to of the water molecule and the nitrogen
period 3 (students to be exposed to the atom of the ammonia molecule to
complete modern periodic table but no explain the formation of H3O+ and OH-
questions will be asked on elements ions in water and NH4+ ion.
beyond period 3 – Argon); The meaning of lone pair; the formation of
• Periodicity and other related hydronium ion and ammonium ion must
properties to be explained on the basis be explained with help of electron dot
of nuclear charge and shells (not diagrams.
orbitals).
3. Study of Acids, Bases and Salts
(Special reference to the alkali metals and halogen
groups). (i) Simple definitions in terms of the molecules
and their characteristic properties.
(ii) Ions present in mineral acids, alkalis and
salts and their solutions; use of litmus and
pH paper to test for acidity and alkalinity.

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• Examples with equation for the highlighted with the help of
ionisation/dissociation of ions of acids, equations.
bases and salts. • Action on addition of Ammonium
• Acids form hydronium ions (only Hydroxide to solution of Ca, Fe, Cu,
positive ions) which turn blue litmus red, Zn, and Pb salts drop by drop in
alkalis form hydroxyl ions (only negative excess. Formation and colour of
ions) with water which turns red litmus hydroxide precipitated to be
blue. highlighted with the help of
• Salts are formed by partial or complete equations.
replacement of the hydrogen ion of an • Special action of Ammonium
acid by a metal. (To be explained with Hydroxide on solutions of copper
suitable examples). salts and sodium hydroxide on
• Introduction to pH scale to test for ammonium salts.
acidity, neutrality and alkalinity by using (ii) Action of alkalis (NaOH, KOH) on
pH paper or Universal indicator. certain metals, their oxides and
(iii) Definition of salt; types of salts. hydroxides.
Types of salts: normal salts, acid salt, basic The metals must include aluminium,
salt, definition and examples. zinc and lead, their oxides and
(iv) Action of dilute acids on salts. hydroxides, which react with caustic
Decomposition of hydrogen carbonates, alkalis (NaOH, KOH), showing the
carbonates, sulphites and sulphides by amphoteric nature of these substances.
appropriate acids with heating if
necessary. (Relevant laboratory work must 5. Mole Concept and Stoichiometry
be done). (i) Gay Lussac’s Law of Combining Volumes;
(v) Methods of preparation of Normal salts with Avogadro’s Law.
relevant equations. (Details of apparatus or • Idea of mole – a number just as a dozen,
procedures not required). a gross (Avogadro’s number).
Methods included are: • Avogadro’s Law - statement and
• Direct combination explanation.
• Displacement • Gay Lussac’s Law of Combining
• Precipitation (double decomposition) Volumes. – Statement and explanation.
• Neutralization of insoluble base • Understanding molar volume- “the
• Neutralisation of an alkali (titration) mass of 22.4 litres of any gas at S.T.P. is
• Action of dilute acids on carbonates and equal to its molar mass”. (Questions will
bi-carbonates. not be set on formal proof but may be
taught for clear understanding).
4. Analytical Chemistry • Simple calculations based on the molar
(i) Action of Ammonium Hydroxide and volume and Gay Lussac’s law.
Sodium Hydroxide on solution of salts: (ii) Refer to the atomicity of hydrogen, oxygen,
colour of salt and its solution; formation nitrogen and chlorine (proof not required).
and colour of hydroxide precipitated for
solutions of salts of Ca, Fe, Cu, Zn and The explanation can be given using
Pb; special action of ammonium equations for the formation of HCl, NH3,
hydroxide on solutions of copper salt and NO.
and sodium hydroxide on ammonium (iii) Vapour Density and its relation to relative
salts. molecular mass:
On solution of salts: • Molecular mass = 2×vapour density
(formal proof not required)
• Colour of salt and its solution. • Deduction of simple (empirical) and
• Action on addition of Sodium molecular formula from:
Hydroxide to solution of Ca, Fe, Cu, (a) the percentage composition of a
Zn, and Pb salts drop by drop in compound.
excess. Formation and colour of (b) the masses of combining
hydroxide precipitated to be elements.
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(iv) Mole and its relation to mass. (v) Applications of electrolysis.
• Relating mole and atomic mass; • Electroplating with nickel and silver,
arriving at gram atomic mass and then choice of electrolyte for electroplating.
gram atom; atomic mass is a number
dealing with one atom; gram atomic • Electro refining of copper.
mass is the mass of one mole of atoms. Reasons and conditions for electroplating;
• Relating mole and molecular mass names of the electrolytes and the electrodes
arriving at gram molecular mass and used should be given. Equations for the
gram molecule – molecular mass is a reactions at the electrodes should be given
number dealing with a molecule, gram for electroplating, refining of copper.
molecular mass is the mass of one mole
of molecules. 7. Metallurgy
• Simple calculations based on relation (i) Occurrence of metals in nature:
of mole to mass, volume and
• Mineral and ore - Meaning only.
Avogadro’s number.
(v) Simple calculations based on chemical • Common ores of iron, aluminium and
equations zinc.
Related to weight and/or volumes of both (ii) Stages involved in the extraction of metals.
reactants and products.
(a) Dressing of the ore – hydrolytic method,
6. Electrolysis magnetic separation, froth flotation
method.
(i) Electrolytes and non-electrolytes.
Definitions and examples. (b) Conversion of concentrated ore to its
oxide- roasting and calcination
(ii) Substances containing molecules only, ions (definition, examples with equations).
only, both molecules and ions.
(c) Reduction of metallic oxides- some can
• Substances containing molecules only
be reduced by hydrogen, carbon and
ions only, both molecules and ions.
carbon monoxide (e.g. copper oxide,
• Examples; relating their composition lead (II) oxide, iron (III) oxide and zinc
with their behaviour as strong and weak oxide) and some cannot (e.g. Al2O3,
electrolytes as well as non-electrolytes. MgO) - refer to activity series). Active
(iii) Definition and explanation of electrolysis, metals by electrolysis e.g. sodium,
electrolyte, electrode, anode, cathode, potassium and calcium. (reference
anion, cation, oxidation and reduction (on only).
the basis of loss and gain of electrons).
Equations with conditions should be
(iv) An elementary study of the migration of given.
ions, with reference to the factors
influencing selective discharge of ions (d) Electro refining – reference only.
(reference should be made to the activity
series as indicating the tendency of metals, (iii) Extraction of Aluminium.
e.g. Na, Mg, Fe, Cu, to form ions) illustrated (a) Chemical method for purifying bauxite
by the electrolysis of: by using NaOH – Baeyer’s Process.
• Molten lead bromide (b) Electrolytic extraction – Hall Heroult’s
process:
• acidified water with platinum electrodes
Structure of electrolytic cell - the
• Aqueous copper (II) sulphate with various components as part of the
copper electrodes; electron transfer at electrolyte, electrodes and electrode
the electrodes.
reactions.
The above electrolytic processes can be Description of the changes occurring,
studied in terms of electrolyte used, purpose of the substances used and the
electrodes used, ionization reaction, anode main reactions with their equations.
reaction, cathode reaction, use of selective
discharge theory, wherever applicable.

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(iv) Alloys – composition and uses. • Laboratory preparation from
ammonium chloride and collection; (the
Stainless steel, duralumin, brass, bronze,
preparation to be studied in terms of,
fuse metal / solder.
setting of the apparatus and diagram,
8. Study of Compounds procedure, observation, collection and
identification)
A. Hydrogen Chloride
• Ammonia from nitrides like Mg3N2 and
Hydrogen chloride: preparation of hydrogen AlN using warm water.
chloride from sodium chloride; refer to the
density and solubility of hydrogen chloride Ammonia from ammonium salts using
(fountain experiment); reaction with alkalies.
ammonia; acidic properties of its solution. The reactions to be studied in terms of
• Preparation of hydrogen chloride from reactants, products, conditions and
sodium chloride; the laboratory method equations.
of preparation can be learnt in terms of • Manufacture by Haber’s Process.
reactants, product, condition, equation,
diagram or setting of the apparatus, • Density and solubility of ammonia
procedure, observation, precaution, (fountain experiment).
collection of the gas and identification. • The burning of ammonia in oxygen.
• Simple experiment to show the density • The catalytic oxidation of ammonia
of the gas (Hydrogen Chloride) – (with conditions and reaction)
heavier than air.
• Its reactions with hydrogen chloride
• Solubility of hydrogen chloride and with hot copper (II) oxide and
(fountain experiment); setting of the chlorine (both chlorine in excess and
apparatus, procedure, observation, ammonia in excess).
inference.
All these reactions may be studied in terms
• Method of preparation of hydrochloric of reactants, products, conditions,
acid by dissolving the gas in water- the equations and observations.
special arrangement and the
mechanism by which the back suction is • Aqueous solution of ammonia - reaction
avoided should be learnt. with sulphuric acid, nitric acid,
hydrochloric acid and solutions of
• Reaction with ammonia iron(III) chloride, iron(II) sulphate,
• Acidic properties of its solution - lead nitrate, zinc nitrate and copper
reaction with metals, their oxides, sulphate.
hydroxides and carbonates to give their • Uses of ammonia - manufacture of
chlorides; decomposition of carbonates, fertilizers, explosives, nitric acid,
hydrogen carbonates, sulphides, refrigerant gas (Chlorofluro carbon –
sulphites. and its suitable alternatives which are
• Precipitation reactions with silver non-ozone depleting), and cleansing
nitrate solution and lead nitrate agents.
solution.
C. Nitric Acid
B. Ammonia Nitric Acid: one laboratory method of
Ammonia: its laboratory preparation from preparation of nitric acid from potassium
ammonium chloride and collection; nitrate or sodium nitrate. Large scale
ammonia from nitrides like Mg3N2 and preparation. Nitric acid as an oxidizing
AlN and ammonium salts. Manufacture by agent.
Haber’s Process; density and solubility of
• Laboratory preparation of nitric acid
ammonia (fountain experiment); aqueous
from potassium nitrate or sodium
solution of ammonia; its reactions with
nitrate; the laboratory method to be
hydrogen chloride and with hot copper (II)
studied in terms of reactants, products,
oxide and chlorine; the burning of ammonia
conditions, equations, setting up of
in oxygen; uses of ammonia.
apparatus, diagram, precautions,
collection and identification.
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• Manufacture of Nitric acid by with the molecular mass or molecular
Ostwald’s process (Only equations with formula.
conditions where applicable). (iv) Simple nomenclature.
• As an oxidising agent: its reaction with Simple nomenclature of the hydrocarbons
copper, carbon, sulphur. with simple functional groups – (double
bond, triple bond, alcoholic, aldehydic,
D. Sulphuric Acid carboxylic group) longest chain rule and
smallest number for functional groups rule
Large scale preparation, its behaviour as an
– trivial and IUPAC names (compounds
acid when dilute, as an oxidizing agent when
with only one functional group).
concentrated - oxidation of carbon and
sulphur; as a dehydrating agent - (v) Hydrocarbons: alkanes, alkenes, alkynes.
dehydration of sugar and copper (II) • Alkanes - general formula; methane
sulphate crystals; its non-volatile nature. (greenhouse gas) and ethane - methods
• Manufacture by Contact Process of preparation from sodium ethanoate
Equations with conditions where (sodium acetate), sodium propanoate
applicable). (sodium propionate), from iodomethane
(methyl iodide) and bromoethane (ethyl
• Its behaviour as an acid when dilute - bromide). Complete combustion of
reaction with metal, metal oxide, metal methane and ethane, reaction of
hydroxide, metal carbonate, metal methane and ethane with chlorine
bicarbonate, metal sulphite, metal through substitution.
sulphide.
• Alkenes – (unsaturated hydrocarbons
• Concentrated sulphuric acid as an with a double bond); ethene as an
oxidizing agent - the oxidation of carbon example. Methods of preparation of
and sulphur. ethene by dehydro halogenation
reaction and dehydration reactions.
• Concentrated sulphuric acid as a
dehydrating agent- (a) the dehydration of • Alkynes - (unsaturated hydrocarbons
sugar (b) Copper (II) sulphate crystals. with a triple bond); ethyne as an
example of alkyne; Methods of
• Non-volatile nature of sulphuric acid - preparation from calcium carbide and
reaction with sodium or potassium 1,2 dibromoethane ethylene dibromide).
chloride and sodium or potassium
nitrate. Only main properties, particularly addition
products with hydrogen and halogen
9. Organic Chemistry namely Cl2, Br2 and I2 pertaining to alkenes
and alkynes.
(i) Introduction to Organic compounds.
• Unique nature of Carbon atom – tetra • Uses of methane, ethane, ethene, ethyne.
valency, catenation. (vi) Alcohols: ethanol – preparation, properties
• Formation of single, double and triple and uses.
bonds, straight chain, branched chain,
• Preparation of ethanol by hydrolysis of
cyclic compounds (only benzene).
alkyl halide.
(ii) Structure and Isomerism. • Properties – Physical: Nature, Solubility,
• Structure of compounds with single, Density, Boiling Points. Chemical:
double and triple bonds. Combustion, action with sodium, ester
• Structural formulae of hydrocarbons. formation with acetic acid, dehydration
Structural formula must be given for: with conc. Sulphuric acid to prepare
alkanes, alkenes, alkynes up to 5 carbon ethene.
atoms. • Denatured and spurious alcohol.
• Isomerism – structural (chain, position) • Important uses of Ethanol.
(iii) Homologous series – characteristics with (vii) Carboxylic acids (aliphatic - mono
examples. carboxylic acid): Acetic acid – properties
Alkane, alkene, alkyne series and their and uses of acetic acid.
gradation in properties and the relationship

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• Structure of acetic acid. 2. Make a solution of the unknown substance: add
sodium hydroxide solution or ammonium
• Properties of Acetic Acid: Physical hydroxide solution, make observations and
properties – odour (vinegar), glacial give your deduction. Warming the mixture may
acetic acid (effect of sufficient cooling to be needed. Choose from substances containing
produce ice like crystals). Chemical Ca2+, Cu2+, Fe2+, Fe3+, Pb2+, Zn2+, NH4+.
properties – action with litmus, alkalis
and alcohol (idea of esterification). 3. Supply a solution of a dilute acid and alkali.
Determine which is acidic and which is basic,
• Uses of acetic acid. giving two tests for each.
4. Add concentrated hydrochloric acid to each of
INTERNAL ASSESSMENT OF
the given substances, warm, make
PRACTICAL WORK
observations, identify any product and make
Candidates will be asked to observe the effect of deductions: (a) copper oxide (b) manganese
reagents and/or of heat on substances supplied to dioxide.
them. The exercises will be simple and may include
the recognition and identification of certain gases EVALUATION
and ions listed below. The examiners will not,
The assignments/project work are to be evaluated by
however, be restricted in their choice to substances
the subject teacher and by an External Examiner.
containing the listed ions.
(The External Examiner may be a teacher nominated
Gases: Hydrogen, Oxygen, Carbon dioxide, by the Head of the school, who could be from the
Chlorine, Hydrogen chloride, Sulphur dioxide, faculty, but not teaching the subject in the
Hydrogen sulphide, Ammonia, Water vapour, section/class. For example, a teacher of Chemistry
Nitrogen dioxide. of Class VIII may be deputed to be an External
Ions: Calcium, Copper, Iron, Lead, Zinc and Examiner for Class X Chemistry projects.)
Ammonium, Carbonate, Chloride, Nitrate, Sulphide,
The Internal Examiner and the External Examiner
Sulphite and Sulphate.
will assess the assignments independently.
Knowledge of a formal scheme of analysis is not
required. Semi-micro techniques are acceptable but Award of Marks (20 Marks)
candidates using such techniques may need to adapt
the instructions given to suit the size of the apparatus Subject Teacher (Internal Examiner) 10 marks
being used. External Examiner 10 marks

Candidates are expected to have completed the The total marks obtained out of 20 are to be sent to
following minimum practical work: the Council by the Head of the school.
1. Action of heat on the following substances: The Head of the school will be responsible for the
(a) Copper carbonate, zinc carbonate online entry of marks on the Council’s CAREERS
portal by the due date.
(b) zinc nitrate, copper nitrate, lead nitrate
Make observations, identify the products and
make deductions where possible (equations not
required).

NOTE: According to the recommendation of International Union of Pure and Applied Chemistry
(IUPAC), the groups are numbered from 1 to 18 replacing the older notation of groups IA …. VIIA, VIII,
IB …… VIIB and 0. However, for the examination both notations will be accepted.
Old IA IIA IIIB IVB VB VIB VIIB VIII IB IIB IIIA IVA VA VIA VIIA 0
notation
New 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
notation

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