Chemistry XI-XII Syllabus 2022 (H2)
Chemistry XI-XII Syllabus 2022 (H2)
Chemistry XI-XII Syllabus 2022 (H2)
CHEMISTRY
GRADES XI-XII
Preface 5
Subject Rationale 8
Concept Map 10
Scheme of Assessment 53
Acknowledgements 64
AKU-EB achieves its vision by developing examination syllabi which inculcate conceptual
thinking and higher order learning and are aligned with National/ trans-provincial curricula
and international standards. AKU-EB revises its syllabi periodically to support the needs of
students, teachers and examiners.
The aims of the syllabus review of SSC and HSSC are to:
• Review the content for inclusion of new knowledge and deletion of obsolete knowledge.
• Review the content for clarity and relevance as per the changing needs of students,
teachers and examiners.
• Enhance and strengthen continuation and progression of content both within and across
grades IX - XII (SCC and HSSC).
During the syllabus review, the needs of all the stakeholders were identified through a needs-
assessment survey. Students and teachers of AKU-EB affiliated schools from across Pakistan
participated in the survey. Thereafter, a revision panel, which consisted of examiners,
teachers of affiliated and non-affiliated schools, teacher trainers and university academicians,
reviewed and revised the syllabus following a planned, meticulous and standardised syllabi
review process.
The syllabus is organised into topics and subtopics. Each subtopic is further divided into
achievable student learning outcomes (SLOs). The SLOs of the cognitive domain are each
assigned a cognitive level on which they have to be achieved. These cognitive levels are
‘knowledge’, ‘understanding’ and ‘application’, the latter also including other higher order
skills. This is followed by the Exam Specification which gives clear guidance about the
weightage of each topic and how the syllabus will be assessed.
The development of the revised syllabus has been made possible by the creativity and
relentless hard work of Curriculum and Examination Development unit and the constant
support provided by all the other units of AKU-EB. We are particularly thankful to
Dr Sohail Qureshi for his very useful feedback on revising the syllabus review process, to
Dr Naveed Yousuf for his continued guidance and support throughout the syllabus revision
process and to Raabia Hirani for leading the syllabi revision. We are also thankful to all the
students and teachers who took part in the needs-assessment survey and to the principals of
AKU-EB affiliated schools who made this endeavour possible by facilitating and
encouraging their teachers to be a part of the survey and the syllabus revision panel.
Dr Shehzad Jeeva
Chief Executive Officer (CEO), Aga Khan University Examination Board
Associate Professor of Practice, Faculty of Arts and Sciences, Aga Khan University
2. The topics of the syllabi are divided into subtopics and student learning outcomes
(SLOs). The subtopics and the SLOs define the depth and the breadth at which each
topic will be taught, learnt and examined. The syllabi also provide enabling SLOs
where needed to scaffold student learning.
3. Each SLO starts with an achievable and assessable command word such as describe,
relate, evaluate, etc. The purpose of the command words is to direct the attention of
teachers and students to specific tasks that the students are expected to undertake in the
course of their studies. The examination questions are framed using the same command
words or their connotations to elicit evidence of these competencies in students’
responses.
4. The topics of the syllabi are grouped into themes derived from the National/ trans-
provincial curricula. The connection between various themes and topics is highlighted
in the ‘concept map’ provided at the beginning of each syllabus. This ensures that
students begin to understand the interconnectedness of knowledge, learn conceptually
and think critically.
5. The SLOs are classified under three cognitive levels: knowledge (K), understanding
(U) and application and other higher order skills (A) for effective planning during
teaching and learning. Furthermore, it will help to derive multiple choice questions
(MCQs), constructed response questions (CRQs) and extended response questions
(ERQs) on a rational basis from the subject syllabi.
6. By focusing on the achievement of the SLOs, these syllabi aim to counter the culture of
rote memorisation as the preferred method of examination preparation. While
suggesting relevant, locally available textbooks for achieving these outcomes, AKU-EB
recommends that teachers and students use multiple teaching and learning resources for
achieving these outcomes.
7. The syllabi follow a uniform layout for all subjects to make them easier for students and
teachers to follow. They act as a bridge between students, teachers and assessment
specialists by providing a common framework of student learning outcomes and exam
specifications.
8. On the whole, the AKU-EB syllabi for Secondary School Certificate (SSC) provide a
framework that helps students to acquire conceptual understanding and learn to
critically engage with it. This lays a solid foundation for HSSC and beyond.
Chemistry is not anything which is restricted to schools, books or the science laboratory, it is
basically found everywhere around us. The air we respire, the food which cooks in the
kitchen, the aroma of perfumes we sense or the storing of food in plants – literally there occur
hundreds and thousands of chemical phenomena every day in life which involves chemistry.
Chemistry is associated with everything we interact with in our daily routine; such as, the
flavourings in our food, the fibres in our clothing, lifesaving drugs for curing threatening
diseases, fertilisers enriching soil fertility, pesticides for protection of crops, cement, glass
and paints for constructing houses to a huge feedstock of petrochemicals for manufacturing
various products. Chemistry could be considered as the core of science subjects, which
interlinks different branches of science and strengthens awareness of the environmental
changes to resolve environmental issues in order to make this planet a better home for all
living organisms.
The AKU-EB Chemistry Syllabus is designed in such a way that it provides essential
theoretical and practical knowledge of real life Chemistry to students. It focuses on
understanding the different themes of Chemistry that will enable students to comprehend the
composition, structure, properties of different materials, their interactions and use in the
synthesis of new products. The syllabus attempts to develop a logical approach for students to
understand different chemical phenomena and solve problems. Furthermore, the use of
multiple learning resources such as models, pictures, animations and various reference books
are encouraged during study to create interest and provide logical understanding of
fundamental concepts of Chemistry.
The study of Chemistry enables an individual to play a vital role in the socioeconomic
development of our country. In recent years, the impact of Chemistry in our society for future
prospects has been excellent. It has opened doors for careers in a variety of professions and
occupations in academia, government, and industry, and in diverse fields such as
environmental sciences, pharmaceuticals, medicine, oceanography, aerospace, engineering
and education. More employment opportunities are available as compared to the past and the
academic sector is becoming well-equipped with highly qualified staff to transfer valuable
knowledge to students. Furthermore, government officials have paid more attention to raise
the standard of higher education in our country, which has resulted in significant provision of
research opportunities to experience problem solving, information handling, organisation,
interpretation and presentation skills in discovering new scientific knowledge. It teaches
practical skills involving the usage of chemicals and sophisticated analytical instruments for
the interpretation of chemical phenomena. The results of the research are of immediate
benefit to the chemists, other scientists in related disciplines and in the industrial sector.
• Engineering
• Medicine
• Pharmacy
• Dentistry
• Nursing
• Veterinary
• Environmental science
• Biotechnology
• Geology
• Biochemistry
• Polymer engineering
• Textile engineering
• Chemical engineering
• Microbiology
The concept map of the syllabus gives an overview of the entire syllabus. The topics and the
student learning outcomes (SLOs) guide regarding the details about what has to be achieved.
And finally, the exam specification guides regarding what will be expected in the
examination.
AKU-EB HSSC Chemistry syllabus is based on the structure of a carbon atom – the most
abundant element in the universe by mass, having a nucleus in the center and 6 electrons
revolving around it. An electrostatic force of attraction holds the protons in the nucleus and
orbiting electrons together. Similarly, Chemistry and its branches are interlinked with each
other. The foundation of Chemistry is represented as the nucleus in a carbon atom and the
rest of the themes of Chemistry are represented by its individual electrons. Furthermore, the
symbols shown for each theme of Chemistry give a quick impression of the concepts it
involves.
Cognitive Level1
Topics and Sub-topics Student Learning Outcomes
K U A
1. Stoichiometry Students should be able to:
1.1 Chemistry as a Quantitative 1.1.1 discuss the significance of Chemistry as a quantitative science *
Science in daily life;
1.2 Mole and Avogadro’s Number 1.2.1 define ‘mole’ and ‘Avogadro’s number’; *
1.2.2 relate the concept of mole with Avogadro’s number; *
1.2.3 calculate the number of following chemical species/ particles, *
i.e.
a. atoms
b. molecules
c. moles
d. ions
e. protons
f. neutrons
g. electrons;
1.2.4 calculate, using a balanced chemical equation, the *
a. interacting moles
b. representative particles
c. masses and volume of gases at STP (22.4 L) and RTP
(24 L);
1.2.5 solve problems based on stoichiometry using mole ratios as *
conversion factor;
1
K = Knowledge, U = Understanding, A = Application and other higher-order cognitive skills
1.4 Excess and Limiting Reagent 1.4.1 deduce the limiting reagent in chemical reactions; *
1.4.2 calculate maximum amount of product produced and amount *
of any unreacted excess reagent, with the help of limiting
reagent in a chemical reaction;
1.5 Theoretical, Actual and 1.5.1 distinguish among theoretical yield, actual yield and *
Percentage Yield percentage yield;
1.5.2 calculate the percentage yield of a product in a chemical *
reaction.
2.2 Planck’s Quantum Theory 2.2.1 explain the relationship among energy, frequency, wavelength *
and wave number using Planck’s quantum theory;
2.6 Dual Nature of Electron 2.6.1 explain the dual nature of electron with reference to de-Broglie *
equation;
2.7 Electronic Configuration 2.7.1 state the rules of electronic configuration, i.e. Aufbau *
principle, Hund’s rule, Pauli’s exclusion principle;
2.7.2 determine electronic configuration of elements based on *
Aufbau principle, Hund’s rule and Pauli’s exclusion principle.
3.2 Shape of Molecules using VSEPR 3.2.1 explain valence shell electron pair repulsion (VSEPR) theory; *
Theory 3.2.2 draw the shape of simple covalent molecules using VSEPR *
theory;
3.3 VBT, MOT and Hybridisation 3.3.1 explain valence bond theory (VBT); *
3.3.2 describe the features of sigma and pi bonds; *
3.3.3 explain hybridisation and its types; *
3.3.4 describe the shapes of simple molecules using orbital *
hybridisation (sp, sp2, sp3);
3.3.5 explain molecular orbital theory (MOT); *
3.3.6 predict the electronic configuration, bond order and magnetic *
properties of homonuclear diatomic molecules with the help of
MOT;
3.3.7 compare VBT and MOT; *
4.2 Absolute Temperature Scale on 4.2.1 explain ‘Absolute Zero’ with reference to Charles’s law; *
the Basis of Charles’s Law 4.2.2 convert temperature into different scales, i.e. *
a. Celsius
b. Fahrenheit
c. Kelvin;
4.3 Ideal Gas Equation 4.3.1 derive ideal gas equation using Boyle’s, Charles’s and *
Avogadro’s law;
4.3.2 calculate the values of ideal gas constant if *
a. pressure is measured in atm and volume in dm3
b. pressure is measured in mm of Hg or torr and volume in
cm3
c. pressure is measured in Nm-2 and volume in m3;
4.4 Deviation from Ideal Behaviour 4.4.1 explain deviation of gases from their ideal behaviour; *
4.5 Vander Waal’s Equation 4.5.1 explain pressure and volume correction for non-ideal gas with *
reference to Vander Waal’s equation;
4.5.2 derive Vander Waal’s equation; *
4.6 Liquefaction of Gases 4.6.1 explain the general principle of liquefaction of gases using *
Joule Thomson’s effect;
4.6.2 discuss Linde’s method for the liquefaction of gases; *
5.2 Intermolecular Forces 5.2.1 explain applications of dipole-dipole forces, hydrogen bonding *
and London forces;
5.2.2 explain the physical properties of liquids, i.e. *
a. evaporation
b. vapour pressure
c. boiling point
d. viscosity
e. surface tension;
5.2.3 explain the following properties of water using the concept of *
hydrogen bonding, i.e.
a. surface tension
b. specific heat
c. vapour pressure
d. heat of vaporisation
e. boiling point
f. when it shows maximum density at 4°C;
6.2 Types and properties of Solids 6.2.1 describe the characteristics of crystalline solids, i.e. *
a. symmetry
b. melting point
c. anisotropy
d. cleavage plane
e. crystal growth
f. geometrical shape
g. habit of crystals;
6.2.2 distinguish between crystalline and amorphous solids; *
6.2.3 differentiate between isomorphism and polymorphism; *
6.2.4 relate polymorphism with allotropy; *
6.2.5 exemplify transition temperature; *
6.3 Crystal Lattice 6.3.1 define ‘unit cell’ and ‘lattice energy’; *
6.3.2 exemplify seven crystal systems; *
6.3.3 explain energy changes in the formation of sodium chloride *
crystal lattice;
8.2 Conjugate Acids and Bases 8.2.1 define the terms ‘conjugate acid’ and ‘conjugate base’; *
8.2.2 compare the strength of conjugate acids and bases; *
8.3 Strengths of Acids and Bases 8.3.1 derive the ionisation constant of water (Kw); *
8.3.2 calculate the pH and pOH of solutions by using the given *
hydrogen or hydroxide ion concentration;
8.3.3 compare the strength of acids and bases using pH and pOH; *
8.3.4 derive the ionisation constants of acid (Ka) and base (Kb); *
8.3.5 show the relationship between Ka and Kb; *
8.3.6 calculate the H3O+ concentration by using the given Ka and *
molar concentration of weak acid;
8.3.7 explain the ‘levelling effect’ with reference to the strength of *
acids;
8.4 Lewis Concept of Acids and 8.4.1 exemplify ‘Lewis acids’ and ‘Lewis bases’; *
Bases 8.4.2 classify compounds (e.g. NH3, AlCl3, BF3, etc.) as Lewis acids *
or bases;
9.3 Collision Theory, Transition State 9.3.1 relate activation energy and activated complex to the rate of *
and Activation Energy reaction;
9.3.2 calculate the initial rate using concentration data of given *
reactions;
9.3.3 draw a labelled energy diagram for a chemical reaction *
representing the activation energy and the effect of catalyst;
9.3.4 describe collision theory; *
9.3.5 explain the effect of concentration, temperature and surface *
area on rate of reaction by using collision theory;
10.2 Concentration Units 10.2.1 calculate the concentration units of solutions, i.e. *
a. percentage composition
b. molarity
c. molality
d. mole fraction
e. parts per million (ppm)
f. parts per billion (ppb)
g. parts per trillion (ppt);
10.3 General Properties of Solution 10.3.1 differentiate between hydrophilic and hydrophobic molecules; *
and Solubility 10.3.2 predict the nature of solutions in liquid phase as miscible, *
immiscible and partially miscible solution;
10.3.3 interpret the solubility graph to check the effect of temperature *
on solubility;
10.4 Raoult’s Law 10.4.1 state Raoult’s law (all three definitions); *
10.4.2 explain relationship between composition and vapour pressures *
of two volatile components using a graph;
10.4.3 discuss ideal and non-ideal solutions with reference to Raoult’s *
law using a graph;
11.2 First Law of Thermodynamics 11.2.1 explain the first law of thermodynamics with the help of daily *
life examples;
11.2.2 relate change in internal energy of system with thermal energy *
at constant volume and pressure;
11.2.3 calculate internal energy and work done of a system by *
applying the first law of thermodynamics;
11.4 Measurement of Enthalpy of a 11.4.1 explain working of a calorimeter (glass and bomb calorimeter); *
reaction 11.4.2 calculate the heat of reaction in a calorimeter from given *
experimental data;
12.3 Types of Electrochemical Cells 12.3.1 define the term ‘cell potential’; *
12.3.2 determine the potential of an electrochemical cell from the *
given standard electrode potential values of substances;
12.4 Faraday’s Law 12.4.1 explain Faraday’s first and second law of electrolysis; *
12.4.2 calculate the quantity of charge passed in an electrochemical *
cell during electrolysis;
12.4.3 calculate the mass or volume of substance produced during *
electrolysis.
Cognitive Level
Topics and Sub-topics Student Learning Outcomes
K U A
13. s- and p-Block Elements Students should be able to:
13.1 Elements and periodicity 13.1.1 describe the demarcation of the periodic table into s, p, d and *
f-blocks;
13.1.2 determine group, period and block of given elements by using *
electronic configuration;
13.1.3 explain the periodicity of physical properties (i.e. atomic *
radius, ionisation energy, electronegativity, electron affinity,
electrical conductivity, melting and boiling points) of elements
within groups and periods in the periodic table;
13.3 Group 1 13.3.1 describe oxidation states and trends in physical properties in *
group 1 elements (i.e. ionisation energy, electronegativity,
atomic radius, melting and boiling point);
13.3.2 describe the chemical reaction of group 1 elements with water, *
oxygen and chlorine;
13.3.3 discuss the trends in solubility of hydroxides, sulphates and *
carbonates of group 1 elements;
13.3.4 discuss the trends in thermal stability of nitrates and *
carbonates of group 1 elements;
13.5 Group 4 13.5.1 describe variation in oxidation states and trends in physical *
properties of group 4 elements (i.e. ionisation energy,
electronegativity, atomic radius, metallic character, melting
and boiling point);
13.5.2 describe the reaction of water with chlorides of carbon, silicon *
and lead;
13.5.3 compare the structure and stability of chlorides of carbon, *
silicon and lead;
13.5.4 describe the molecular structure of CO2 and SiO2; *
13.5.5 discuss the acid-base characteristics of oxides of group 4 *
elements;
13.6 Group 7 13.6.1 discuss oxidation states and trends in physical properties of *
group 7 elements (i.e. atomic radius, electronegativity,
electron affinity, bond energy, melting and boiling point);
14.2 Electronic Structure 14.2.1 explain anomalous behaviour of chromium and copper with *
respect to electronic configuration;
14.2.2 determine the electronic configuration of elements and ions of *
d-block;
14.3 Chemistry of Some Specific 14.3.1 describe redox reactions and uses of vanadium, chromium, *
Transition Elements copper, manganese and iron as catalyst;
14.3.2 describe properties of alloys with reference to the metals that *
compose them;
14.3.3 describe the reaction of K2Cr2O7 with FeSO4, and H2S; *
14.3.4 describe the reaction of KMnO4 with FeSO4, and H2S; *
15.2 Classification of Organic 15.2.1 classify organic compounds on the basis of their structure; *
Compounds 15.2.2 identify a molecule’s functional group (i.e. alkane, alkene, *
alkyne, arene, halide, alcohol, ether, amine, nitrile, nitro,
sulphide, sulphoxide, sulphone, thiol, aldehyde, ketone,
carboxylic acid, ester, acid amide, acid chloride, acid
anhydride);
16.2 Types of Organic Reactions 16.2.1 define different types of organic reactions, i.e. *
a. substitution reaction
b. elimination reaction
c. addition reaction
d. radical reaction
16.3 Alkanes 16.3.1 explain unreactive nature of alkanes towards polar reagents; *
16.3.2 explain homolytic and heterolytic fission, free radical *
initiation, propagation and termination;
16.3.3 describe the mechanism of free radical substitution with *
reference to methane and ethane;
16.4 Alkenes 16.4.1 describe the preparation of ethene (using chemical equations) *
from:
a. dehydration of alcohol
b. dehydrohalogenation of alkyl halide;
16.4.2 describe the reactions of ethene, i.e. *
a. hydrogenation
b. hydration
c. hydrohalogenation
d. halogenation
e. halohydration
f. epoxidation
g. ozonolysis
h. polymerisation;
16.6 Benzene and Substituted Benzene 16.6.1 compare the reactivity of benzene with alkene and alkane; *
16.6.2 describe the mechanism of electrophilic substitution reaction *
of benzene;
16.6.3 explain orientation in benzene with reference to resonating *
structures, i.e. effect of ortho, meta and para directing groups
in electrophilic substitution reactions;
16.6.4 discuss the chemistry of benzene and methyl benzene by *
nitration, sulphonation, halogenation, Friedal-Crafts alkylation
and acylation.
17.2 Nucleophilic Substitution 17.2.1 describe the mechanism of nucleophilic substitution (SN1 and *
Reaction SN2) reactions;
17.2.2 discuss carbocation and its stability; *
17.2.3 compare SN1 and SN2 reactions; *
17.2.4 deduce the mechanism of nucleophilic substitution (SN1 and *
SN2) reaction for the given alkyl halide;
17.2.5 identify nucleophile (base), substrate and leaving group in the *
given nucleophilic substitution reactions;
17.3 Elimination Reaction 17.3.1 describe the mechanism of elimination (E1 and E2) reaction; *
17.3.2 compare E1 and E2 reaction; *
17.3.3 deduce the mechanism of elimination (E1 and E2) reaction for *
the given alkyl halide;
17.3.4 compare substitution reaction with elimination reaction; *
17.4 Organo-Metallic Compounds 17.4.1 describe the preparation and reactivity of Grignard reagent; *
(Grignard Reagent) 17.4.2 describe chemical reaction of Grignard reagent with *
aldehydes, ketones, esters and carbon dioxide;
18.2 Phenols 18.2.1 apply IUPAC and trivial system for naming different phenols; *
18.2.2 discuss the physical properties, structure and acidic *
characteristics of phenol (with reference to its resonance only);
18.2.3 describe the preparation of phenols from the given compounds *
(benzene sulphonic acid, chlorobenzene, acidic oxidation of
cumene and hydrolysis of diozomium salts) using chemical
equations;
18.2.4 discuss the reactivity of phenol with reference to electrophilic *
aromatic substitution, reaction with Na metal and oxidation;
18.2.5 differentiate between alcohols and phenols; *
19.2 Physical Properties 19.2.1 explain the physical properties of aldehydes and ketones; *
19.3 Preparation of Aldehydes and 19.3.1 describe the preparation of aldehydes and ketones by: *
Ketones a. ozonolysis of alkene
b. hydration of alkyne
c. oxidation of alcohol
d. Friedal Crafts acylation of aromatic compound;
19.4 Reaction of Aldehydes and 19.4.1 describe the base catalysed nucleophilic addition reaction of *
Ketones aldehydes and ketones, i.e.
a. addition of hydrogen cyanide
b. addition of Grignard reagent
c. addition of sodium bisulphate
d. Aldol condensation
e. Cannizzaro’s reaction
f. haloform (iodoform) reaction;
19.5 Uses and Effects 19.5.1 discuss the uses of formaldehyde in daily life; *
19.5.2 discuss the health hazards associated with the exposure to *
formalin.
20.2 Structure and Physical Properties 20.2.1 describe the structure and physical properties (solubility, *
melting point and boiling point) of carboxylic acid;
20.2.2 draw the structure of given compounds of carboxylic acids and *
their derivatives;
20.4 Preparation of Carboxylic Acid 20.4.1 describe the preparation of carboxylic acid by Grignard *
reagent, hydrolysis of nitriles, oxidation of primary alcohol,
aldehydes and alkyl benzene using chemical equations;
20.6 Reactions of Carboxylic Acid 20.6.1 describe the preparation of acyl halides, acid anhydrides, *
esters and amides;
20.6.2 describe the inter-conversion reactions of the carboxylic acid *
derivatives (acyl halides, acid anhydrides, esters and amides);
20.7 Uses 20.7.1 identify carboxylic acids present in fruits and vegetables; *
20.7.2 describe the uses of carboxylic acids, i.e. in plastic, leather, *
rubber, soap industries and as preservatives in food and food
products.
21.2 Enzymes 21.2.1 describe the role of enzymes as biological catalyst, i.e. in *
digestion of food;
21.2.2 explain the factors that affect enzyme activity; *
21.2.3 explain the role of inhibitors in enzyme catalysed reactions; *
21.3 Nucleic Acids 21.3.1 differentiate between the structure of DNA and RNA; *
21.3.2 describe the role of *
a. DNA in storing genetic information
b. RNA in terms of protein synthesis;
21.4 Minerals of Biological 21.4.1 describe the role of iron and phosphorous as nutrients. *
Significance
22.2 Safety Measurement 22.2.1 list safety precautions that should be followed in chemical *
industries;
22.5 Synthetic Polymers (PVC and 22.5.1 describe the chemical processes of addition and condensation *
Nylon) polymerisation;
22.5.2 describe the formation and uses of polyvinyl chloride (PVC) *
and nylon;
23.2 Water Pollution and Water 23.2.1 describe the parameters of water analysis; *
Treatment 23.2.2 explain the methods of water purification, i.e. raw water *
treatment, sewage treatment, zeolite process and reverse
osmosis;
2. Atomic Structure 7 3 12 4 19
Theories of Covalent Bonding and Shapes
3. 4 2 14 4 20
of Molecules
4. States of Matter I: Gases 7 1 12 6 19
7. Chemical Equilibrium 4 5 3 8 16
9. Chemical Kinetics 4 3 6 4 13
11. Thermochemistry 6 3 6 5 14
12. Electrochemistry 4 3 6 8 17
Topic
Topics Marks Distribution Total
No.
Marks
MCQs CRQs ERQs
1. Stoichiometry 4 7 Marks
Choose any
15
12. Electrochemistry 4 ONE from
TWO
Total 4 Marks
2. Atomic Structure 4 8
(1 CRQ)
Theories of Covalent Bonding Total 5 Marks
3. 5 10
and Shapes of Molecules (2 CRQs)
4. States of Matter I: Gases 5 5
5. States of Matter II: Liquids 5 5
6. States of Matter III: Solids 5 5
Total 4 Marks
7. Chemical Equilibrium 3 7
(1 CRQ)
8. Acids, Bases and Salts 4 7 Marks
Choose any
15
10. Solutions and Colloids 4 ONE from
TWO
Total 4 Marks
9. Chemical Kinetics 3 7
(1 CRQ)
Total 4 Marks
11. Thermochemistry 4 8
(1 CRQ)
Total 50 21 14 85
Practical* 15
Total 100
16. Hydrocarbons 6 1 16 0 17
Topic
Topics Marks Distribution Total
No.
Marks
MCQs CRQs ERQs
13. s- and p-Block Elements 5 5
14. d- and f- Block Elements 4 4
Total 3 Marks
15. Organic Compounds 3 6
(1 CRQ)
16. Hydrocarbons 4 7 Marks
Choose any
15
23. Environmental Chemistry 4 ONE from
TWO
17. Alkyl halides and Amines 4 7 Marks
Carbonyl Compound II: Choose any
15
20. Carboxylic Acid and 4 ONE from
Functional Derivatives TWO
Total 4 Marks
18. Alcohols, Phenols and Ethers 5 9
(1 CRQ)
Carbonyl Compound I: Total 4 Marks
19. 5 9
Aldehydes and Ketones (1 CRQ)
Total 3 Marks
21. Biochemistry 4 7
(1 CRQ)
Total 3 Marks
22. Industrial Chemistry 5 8
(1 CRQ)
Total 4 Marks
24. Analytical Chemistry 3 7
(1 CRQ)
Total 50 21 14 85
Practical* 15
Total 100
• Multiple Choice Question (MCQ) requires candidates to choose one best/ correct answer from
four options for each question. Each MCQ carries ONE mark.
• Constructed Response Question (CRQ) requires students to respond with a short text (few
phrases/ sentences), calculations or diagrams.
• Extended Response Question (ERQ) requires students to answer in a more descriptive form. The
answer should be in paragraph form, with diagrams where needed, and address all parts of the
question.
• There will be two examinations, one at the end of grade XI and one at the end of
grade XII.
• In each grade, the theory paper will be in two parts: paper I and paper II. Both papers will be
of duration of 3 hours.
• Paper I theory will consist of 50 compulsory, multiple choice items. These questions will
involve four response options.
• Paper II theory will carry 35 marks and consist of a number of compulsory, structured
questions and a number of extended response questions. Each extended response question
will be presented in an either/or form.
• All constructed response questions will be in a booklet which will also serve as an answer
script.
*Practical:
• In each grade, practical examination will be conducted separate from the theory paper and will
consist of 15 marks.
• Practical examination will be based on the list of practical activities given in the examination
syllabus. Schools may design their own practical manuals based on these activities.
• Practical journal/ portfolio should be developed by students and endorsed by a figure of
authority, such as a teacher or principal, and submitted at the time of the practical
examination.
• It is essential for each school to equip its laboratories with chemicals, instruments, apparatus,
specimens etc. according to the requirements of the practical activities. Each school will be
responsible to make sure that each student is provided the opportunity to do the practical
activities.
SLO
S. No. PRACTICAL ACTIVITY EQUIPMENT CHEMICAL
No.
Topic 1: Stoichiometry
1. 1.4.2 Estimate the amount of Ba +2 in the Analytical balance, oven, funnel, wash Distilled water, potassium chromate
given solution of BaCl2 gravimetrically. bottle, Whatman filter paper No. 42, solution, barium chloride solution
glass rod, beakers, desiccators, pipette,
burner, match box, safety goggles
5. 8.1.4 Determine the percentage of NaOH in Burette, pipette, funnel, conical flasks, Phenolphthalein, 0.1M NaOH, 0.1M
the given solution (such as a mixture of beakers, iron stand with clamp HCl, distilled water, solution
NaCl and NaOH or a sample of soap containing 8 g of a mixture of NaCl
solution) by volumetric method. and NaOH/ 250 mL solution of 10 g
soap.
6. 8.1.4 The given solution contains 6 g of Burette, pipette, funnel, conical flasks, Methyl orange,
Na2CO3 dissolved per dm 3 . Determine beakers, iron stand with clamp 0.1M Na2CO3, 0.1M HCl, distilled
the percentage purity of the sample water, solution of 6 g of Na2CO3 in 1L.
solution by volumetric method.
7. 8.1.4 Determine the value of X by volumetric Burette, pipette, funnel, conical flasks, Phenolphthalein, 0.1M NaOH, 0.1M
method in the given sample of 6.3 g of beakers, iron stand with clamp (COOH)2.2H2O, distilled water
(COOH) 2 . XH 2 O dissolved per L.
8. 8.1.4 Determine the solubility of oxalic acid Burette, pipette, funnel, conical flasks, Phenolphthalein, 0.1M NaOH, 0.1M
at room temperature volumetrically. beakers, iron stand with clamp (COOH)2.2H 2 O, distilled water
12. 12.1.8 Determine the amount of iron in the Burette, pipette, funnel, conical flasks, 0.05M FeSO 4 solution, 0.01M KMnO4
given sample volumetrically. beakers, iron stand with clamp, test tube solution, dilute H2SO4, distilled water
13. 12.1.8 Determine the percentage composition Burette, pipette, funnel, conical flask, Solution mixture of K2C2O4 and
volumetrically of a solution mixture of beakers, iron stand with clamp, test tube K2SO4, 0.01M KMnO4 solution, dilute
K2C2O4 and K2SO4. H2SO4, distilled water
14. 12.1.8 Determine the solubility of Mohr’s salt Burette, pipette, funnel, conical flasks, 0.05M Mohr’s salt solution, 0.01M
at room temperature volumetrically. beakers, iron stand with clamp, test tube KMnO4 solution, dilute H2SO4,
distilled water
SLO
S. No. PRACTICAL ACTIVITY EQUIPMENT CHEMICAL
No.
Topic 13: s- and p-Block Elements
1. 13.2.4, Detect the following cations: NH +4 , Test tubes, test tube holder, test tube rack, Sodium hydroxide, ammonium
delivery tube, measuring cylinder, match hydroxide, dilute acids, barium, lead,
13.3.4, Mg 2 + , Al 3+ , Ca 2 + , Ni 2+ , Co 2 + , Fe 2 + ,
3+ 2+ 2+ 2+ 2+ box, wooden splint, Bunsen burner/ spirit silver salt solutions, Aluminium foil,
13.4.2, Fe , Cu , Zn , Ba , Pb . 2 − lamp, safety goggles, glass rod, filter lime water and other necessary
Detect the following anions: CO 3 , paper, litmus paper chemical solutions for the
13.4.3,
NO 3− , NO −2 , SO 24 − , SO 32 − , Cl − , Br − , identification of these ions and gases
13.5.5
I − , CrO 24 − . Perform tests for the
and
13.6.2 following gases: NH 3 , CO 2 , Cl 2 , H 2 ,
O 2 , SO 2 .
3. 15.2.2 Detect elements in an organic Test tubes, test tube holder, test tube For Lassaigne’s solution: Sodium
compound (nitrogen, sulphur and rack, safety goggles, Bunsen burner/ metal, organic compound containing
halogen). spirit lamp, tripod stand, wire guaze, nitrogen, sulphur and halogen, distilled
china dish, dropper water.
5. 17.5.7 Prepare azo dye from amine. Test tubes, test tube rack, test tube Amine, phenol, hydrochloric acid, ice,
holder, measuring cylinder, balance, sodium nitrite, alcohol, distilled water
filter paper, funnel
7. 18.2.2 Identify the phenol functional group. Test tubes, test tube holder, test tube Litmus solution, ferric chloride solution
rack, measuring cylinder, safety goggles.
Topic 20: Carbonyl Compound II: Carboxylic Acid and Functional Derivatives
9. 20.2.1 Identify the carboxylic acid functional Test tubes, beakers, balance, measuring Dilute sodium hydroxide, saturated
group. cylinders, funnel, filter paper potassium bicarbonate
We would like to thank Dr Syed Majid Khalil, Former Specialist, Chemistry, AKU-EB, for
taking the subject lead and Afreen Kanwal, Lead Specialist, Chemistry, AKU-EB, for
taking the co-lead for the revision of the HSSC Chemistry syllabus syllabus and Uroosa
Aslam, Specialist Chemistry for taking the lead during the development of Exam Specification
2023.
We are particularly thankful to the syllabus revision panel for their time, commitment and
effort in revising the syllabus. The panel included:
• Mahwish Kanwal
Aga Khan Higher Secondary School, Karachi
• Ghazanfar Sultan
BVS Parsi High School, Karachi
We also thank the following post-revision reviewers for their feedback on relevance of the
content, skills and resources of the revised syllabus:
• Muhammad Faisal
IISAAR Foundation Higher Secondary School, Karachi
Furthermore, we thank External Reviewer, institution for reviewing the syllabus for higher
education preparedness, ensuring that the syllabus includes adequate skills and content to
effectively prepare students for the next level of education.
• Dr Rehana Ifzal
Professor
St. Joseph's College for Women, Karachi
• Administrative Support:
Hanif Shariff, Associate Director, Operations
Raheel Sadruddin, Manager, Administration, and team
• Design Support:
Karim Shallwanee, Former Associate, Communications
Hatim Yousuf, Specialist, Communications
We would like to thank the students and teachers of affiliated schools from across Pakistan
who gave their valuable feedback at various stages of the review process.
We also thank Shahid Arwani, Assistant AKU-EB, Anusha Aslam, Assistant AKU-EB,
Tabassum Ali Senior Assistant, for data compilation and formatting. In addition, we thank
Noshaba Hameed, Assistant AKU-EB, Ammara Dawood and Lubna Anis for their support
during formatting.