Revised Syllabus and Evaluation – ICSE CHEMISTRY – Academic year 2022-2023
There will be one written paper of two hours duration of 80 marks and Internal Assessment
of practical work carrying 20 marks.
Note: All chemical processes / reactions should be studied with reference to the reactants, products, conditions, observation, the (balanced) equations and diagrams.
1. Periodic Properties and variations of Properties
– Physical and Chemical
(i) Periodic properties and their variations in groups and periods.
Definitions and trends of the following periodic properties in groups and periods should be studied:
·
atomic size
·
metallic character
·
non-metallic character
·
ionisation potential
·
electron affinity
·
electronegativity
(ii) Periodicity on the basis of atomic number for elements.
·
The study
of modern periodic table up to period 4(students to be exposed
to the complete modern periodic
table but no questions will be asked on elements
beyond period 4 - Calcium).
·
Periodicity
and other related properties to be explained
on the basis of nuclear
charge and shells (not orbitals).
(Special reference to the alkali
metals, alkaline earth
metals, halogens and inert
gases).
2. Chemical Bonding
Electrovalent, covalent and co-ordinate bonding, structures of various compounds, Electron dot structure.
(a) Electrovalent bonding:
·
Electron dot structure of Electrovalent compounds NaCl, MgCl2, CaO.
·
Characteristic
properties of electrovalent compounds
– state of existence, melting and
boiling points, conductivity (heat and electricity), dissociation in solution and in molten
state to be linked with electrolysis.
(b) Covalent Bonding:
·
Electron dot structure of covalent molecules on the basis
of duplet and octet of electrons (example: hydrogen, oxygen, chlorine, nitrogen, ammonia, carbon tetrachloride, methane.
· Polar Covalent compounds – based on difference in electronegativity:
Examples – HCl, NH3 and H2O including structures.
·
Characteristic properties of Covalent compounds – state of existence, melting and boiling points, conductivity (heat and electricity), ionisation in solution.
Comparison of Electrovalent and Covalent
compounds.
(c) Coordinate Bonding:
·
Definition
·
The lone
pair effect of the oxygen atom of the
water molecule and the nitrogen atom of
the ammonia molecule to explain the formation of H3O+ and OH- ions in water and NH4+ ion.
The
meaning of lone pair; the formation of hydronium
ion and ammonium ion must be explained with the help of electron
dot diagrams.
3. Study of Acids, Bases and Salts
(i)
Simple definitions, classification 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.
·
Examples with equation for the ionisation/dissociation of acids, bases
and salts.
·
Acids form hydronium ions (only positive ions) which turn blue litmus red, alkalis form hydroxyl ions (only negative
ions) with water which turns red litmus blue.
·
Salts are formed by partial or complete replacement of the hydrogen
ion of an acid by a metal or ionic definition of salt. (To be explained with suitable examples).
·
Introduction
to pH scale to test for acidity, neutrality and alkalinity by using pH paper or Universal indicator and common acid base indicators.
(iii) Types of salts: normal salts, acid salt, basic salt, definition and examples.
(iv) Action of dilute acids on salts.
Decomposition of hydrogen carbonates, carbonates, sulphites and sulphides by appropriate acids with heating if necessary. (Relevant laboratory work must be done).
4. Analytical Chemistry
(i) Action of Ammonium Hydroxide and Sodium Hydroxide on solution of salts: colour of salt and its solution; formation and colour of hydroxide precipitated for solutions of salts of Ca, Fe, Cu, Zn and Pb; special action of ammonium hydroxide on solutions of copper salt and sodium hydroxide on ammonium salts.
On solution of salts:
·
Colour of salt and its solution.
·
Action on addition of Sodium Hydroxide to solution of Ca, Fe, Cu, Zn, and Pb salts drop by drop and in excess. Formation
and colour of hydroxide precipitated to be highlighted with the help of equations.
·
Action on addition of Ammonium Hydroxide to solution of Ca, Fe, Cu, Zn, and Pb salts drop by drop and in excess.
Formation and colour of hydroxide precipitated to be highlighted with the help of equations.
·
Special action of Ammonium
Hydroxide on solutions
of copper salts and sodium hydroxide on ammonium salts.
(ii) Action of alkalis (NaOH, KOH) on certain metals, their oxides and hydroxides.
The metals must
include aluminium, zinc and lead, their oxides and hydroxides, which react with caustic alkalis (NaOH, KOH), showing the amphoteric nature of these substances.
5. Mole Concept and Stoichiometry
(i) Gay Lussac’s Law of Combining Volumes
Statement and explanation with numerical problems.
(ii) Vapour Density
and its relation to relative
molecular mass:
·
Molecular mass = 2´vapour density (formal proof not required)
·
Deduction of simple (empirical) and molecular formula
from:
(a)
the percentage composition of a compound.
(b) the masses of combining elements.
6. Electrolysis
(i)
Electrolytes and non-electrolytes. Definitions and examples.
(ii) Substances containing molecules only, ions only, both molecules and ions.
·
Substances containing molecules only ions only,
both molecules and ions.
·
Examples:
relating their composition with their behaviour
as strong and weak electrolytes as well as non-electrolytes.
(iii) Definition and explanation of electrolysis, electrolyte, electrode, anode, cathode, anion,
cation, oxidation and reduction (on the basis of loss and gain of electrons).
(iv)An elementary study of the migration of ions, with reference to the factors influencing selective discharge of ions (reference should be made to the activity series as indicating the tendency of metals, e.g., Na, Mg, Fe, Cu, to form ions) illustrated by the electrolysis of:
·
Molten lead bromide
·
acidified water
with platinum electrodes
·
Aqueous copper (II) sulphate with inert electrode, copper electrodes; electron
transfer at the electrodes.
The above electrolytic processes
can be studied in terms of electrolyte used, electrodes used, ionization reaction, anode reaction, cathode reaction, use of
selective discharge theory, wherever applicable.
(v) Applications of electrolysis.
·
Electroplating with nickel and silver, choice of
electrolyte for electroplating.
·
Electro refining
of copper.
Reasons
and conditions for electroplating; names
of the electrolytes and the electrodes used should be given. Equations for the reactions at the electrodes should be
given for electroplating, refining of
copper.
7. Metallurgy
(i) Occurrence of metals in nature:
·
Mineral
and ore - Meaning only.
·
Common ores of iron, aluminium and zinc.
(ii) Extraction of Aluminium.
(a) Chemical method for purifying bauxite by using
NaOH – Baeyer’s Process.
(b)
Electrolytic
extraction – Hall Heroult’s process:
Structure of electrolytic cell - the various components as part of the electrolyte, electrodes and electrode reactions.
Description of the changes occurring, purpose of the substances used and the main reactions with their equations.
(iii) Alloys – composition and uses.
Stainless steel, duralumin, magnalium, brass, bronze, fuse metal / solder.
8. Study of Compounds
A. Hydrogen
Chloride
Hydrogen chloride: preparation of hydrogen chloride from sodium chloride; refer to the density and solubility of hydrogen chloride (fountain experiment); reaction with ammonia; acidic properties of its solution.
·
Preparation of hydrogen chloride
from sodium chloride; the
laboratory method of preparation can
be learnt in terms of reactants, product,
condition, equation, diagram
or setting of the apparatus, procedure, observation, precaution, collection of the
gas and identification
/tests.
·
Simple
experiment to show the density of the gas (Hydrogen Chloride)
–heavier than air.
·
Solubility
of hydrogen chloride (fountain experiment); setting
of the apparatus, procedure, observation, inference.
· Method of preparation of hydrochloric acid by dissolving the gas in water- the special funnel arrangement and the mechanism by which the back suction is avoided should be learnt.
·
Reaction
with ammonia
·
Acidic properties of its solution
- reaction with metals, their oxides, hydroxides
and carbonates to give their chlorides; decomposition of carbonates, hydrogen
carbonates, sulphides,
sulphites.
·
Reaction of Manganese dioxide
with concentrated HCl.
·
Precipitation
reactions with silver nitrate solution
and lead nitrate solution.
B. Ammonia
Ammonia: its laboratory preparation from ammonium chloride and collection; ammonia from nitrides like Mg3N2 and AlN and ammonium salts. Manufacture by Haber’s Process; density and solubility of ammonia (fountain experiment); aqueous solution of ammonia; its reactions with hydrogen chloride and with hot copper (II) oxide and lead monoxide and chlorine; the burning of ammonia in oxygen.
Laboratory preparation from ammonium chloride and collection; (the preparation to be studied in terms of, setting of the apparatus and diagram, procedure, observation, collection and identification/tests.)
·
Ammonia from nitrides like Mg3N2 and AlN using warm water.
Ammonia from ammonium
salts using alkalies.
The reactions
to be studied in terms of reactants, products, conditions and equations.
·
Manufacture by Haber’s Process.
·
Density and solubility of ammonia
(fountain experiment).
·
The burning
of ammonia in oxygen.
·
The catalytic
oxidation of ammonia
(with conditions and reaction)
·
Its
reactions with hydrogen chloride and with
hot copper (II) oxide, lead monoxide and chlorine
(both chlorine in excess and ammonia in excess).
All these reactions may be studied in terms of reactants, products, conditions, equations and observations.
·
Aqueous
solution of ammonia - reaction with sulphuric
acid, nitric acid, hydrochloric acid and solutions
of iron(III) chloride,
iron(II) sulphate, lead nitrate, zinc nitrate and copper sulphate.
C. Nitric Acid
Nitric Acid: one laboratory method of preparation of nitric acid from potassium nitrate or sodium nitrate. Large scale preparation. Nitric acid as an oxidizing agent.
· Laboratory preparation of nitric acid from potassium nitrate or sodium nitrate; the laboratory method to be studied in terms of reactants, products, conditions, equations, setting up-of-apparatus,diagram, precautions, collection and identification/tests.
·
Manufacture
of Nitric acid by Ostwald’s process
(Only equations with conditions where applicable).
· As an oxidising agent: its reaction with copper, carbon, sulphur.
·
Thermal decomposition of nitrates.
D. Sulphuric Acid
Large scale preparation, its behaviour as an acid when dilute, as an oxidizing agent when concentrated - oxidation of carbon, sulphur and copper; as a dehydrating agent - dehydration of sugar (cane sugar/glucose) and copper (II) sulphate crystals; its non-volatile nature.
·
Manufacture by Contact Process
Equations with conditions where applicable).
·
Its behaviour as an acid when
dilute - reaction
with metal, metal oxide, metal hydroxide, metal carbonate, metal bicarbonate, metal sulphite,
metal sulphide.
·
Concentrated sulphuric
acid as an oxidizing agent -
the oxidation of carbon sulphur and copper.
·
Concentrated sulphuric acid as a dehydrating agent- (a) the dehydration of sugar (b) Copper
(II) sulphate crystals.
· Non-volatile nature of sulphuric acid - reaction with sodium or potassium chloride and sodium or potassium nitrate.
·
Tests for dilute and concentrated sulphuric
acid.
9. Organic Chemistry
(i) Introduction to Organic compounds.
·
Unique
nature of Carbon atom – tetra valency, catenation.
·
Formation
of single, double and triple bonds,
straight chain, branched chain, cyclic compounds (only benzene).
(ii) Structure and Isomerism.
·
Structure of compounds with single, double and triple bonds.
·
Structural formulae
of hydrocarbons. Structural formula must be given for: alkanes, alkenes, alkynes, alcohols, aldehydes and
carboxylic acid up to 5 carbon atoms.
·
Isomerism – structural (chain,
position)
(iii) Homologous series – characteristics with examples.
Alkane, alkene, alkyne series and their gradation in properties and the relationship with the molecular mass or molecular formula.
(iv) Simple nomenclature.
Simple nomenclature of the hydrocarbons with simple functional groups – (double bond, triple bond, alcoholic, aldehydic, carboxylic group) longest chain rule and smallest number for functional groups rule – trivial and IUPAC names (compounds with only one functional group).
(v) Hydrocarbons: alkanes, alkenes, alkynes.
·
Alkanes - general formula; methane (greenhouse gas) and ethane - methods of preparation from sodium ethanoate
(sodium acetate), sodium propanoate (sodium
propionate), from iodomethane (methyl iodide) and bromoethane (ethyl
bromide). Complete combustion of methane and ethane,
reaction of methane and ethane with chlorine
through substitution.
·
Alkenes – (unsaturated hydrocarbons with a double bond); ethene as an example. Methods
of preparation of ethene
by dehydro halogenation reaction and dehydration reactions.
·
Alkynes -
(unsaturated hydrocarbons with a
triple bond); ethyne as an example of alkyne; Methods
of preparation from calcium
carbide and 1,2 dibromoethane ethylene dibromide).
Only
main properties, particularly addition products
with hydrogen and halogen namely Cl2, Br2 and I2 pertaining to alkenes and alkynes.
INTERNAL ASSESSMENT OF PRACTICAL WORK
Candidates will be asked to observe the effect of reagents on substances supplied to them. The exercises will be simple and may include the recognition and identification of certain gases and ions listed below. The examiners will not, however, be restricted in their choice to substances containing the listed ions.
Gases: Hydrogen, Oxygen, Carbon dioxide, Chlorine, Hydrogen chloride, Sulphur dioxide, Hydrogen sulphide, Ammonia, Water vapour, Nitrogen dioxide.
Ions: Calcium, Copper, Iron, Lead, Zinc and Ammonium, Carbonate, Chloride, Nitrate, Sulphide, Sulphite and Sulphate.
Knowledge of a formal scheme of analysis is not required. Semi-micro techniques are acceptable but candidates using such techniques may need to adapt the instructions given to suit the size of the apparatus being used.
Candidates are expected to have completed the following minimum practical work:
1. Make a solution of the unknown substance: add sodium hydroxide solution or ammonium hydroxide solution, make observations and give your deduction. Warming the mixture may be needed. Choose from substances containing Ca2+, Cu2+, Fe2+, Fe3+, Pb2+, Zn2+, NH4+.
2. Determine which of the given solutions is acidic and which is basic, giving two tests for each.
3. Add concentrated hydrochloric acid to each of the given substances, warm, make observations, identify any product and make deductions: (a) copper oxide (b) manganese dioxide.
EVALUATION
Award of Marks (20 Marks)
Subject Teacher (Internal Examiner) 10 marks External Examiner 10 marks
The total marks obtained out of 20 are to be sent to the Council by the Head of the school.
The Head of the school will be responsible for the online entry of marks on the Council’s CAREERS portal by the due date.
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 notation |
IA |
IIA |
IIIB |
IVB |
VB |
VIB |
VIIB |
VIII |
IB |
IIB |
IIIA |
IVA |
VA |
VIA |
VIIA |
0 |
||
New notation |
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
10 |
11 |
12 |
13 |
14 |
15 |
16 |
17 |
18 |
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