CHSE Odisha Elective Chemistry study materials
CHSE Odisha Elective Chemistry study resources

CHSE Odisha Elective Chemistry study plan

CHSE Odisha Elective Chemistry · Give each week a clear focus.

8 weeks · About 7 hours per week

Week 1

d- and f-Block Elements and Coordination Compounds

  • Write IUPAC names and formulas for at least 20 coordination compounds covering cationic, anionic and neutral complexes, bridging ligands and metals in variable oxidation states.

  • Distinguish ionization, hydrate, linkage, coordination, geometrical and optical isomerism, giving one worked example of each.

  • Draw octahedral and tetrahedral crystal-field splitting diagrams for at least 10 complexes and calculate their spin-only magnetic moments in Bohr magnetons.

  • Outline the laboratory preparation and five characteristic reactions each of potassium permanganate and potassium dichromate in acidic, basic and neutral media.

  • Explain lanthanoid contraction and its consequences for atomic radius, ionisation enthalpy and chemistry of later transition metals; list four lanthanoid–actinoid differences.

Your checkpoint

A two-page coordination-chemistry and d/f-block summary sheet plus a 25-question self-test scored at 80% or above.

Week 2

Haloalkanes, Haloarenes, Alcohols, Phenols and Ethers

  • Classify given haloalkanes and haloarenes as primary, secondary, tertiary, allylic, benzylic or vinylic, and predict their relative reactivity.

  • Compare SN1, SN2, E1 and E2 pathways for named substrates, specifying rate law, stereochemical outcome, solvent and leaving-group effects.

  • Map the preparation and at least six reactions each for alcohols, phenols and ethers, including Lucas test, Victor Meyer test, Reimer–Tiemann, Kolbe and Williamson synthesis.

  • Explain why phenol is more acidic than alcohols and why haloarenes resist nucleophilic substitution, using resonance and hybridisation arguments.

  • Solve 15 named conversions involving halogenation, dehydrohalogenation, ether cleavage and aromatic substitution.

Your checkpoint

A 30-card reaction map covering haloalkanes, haloarenes, alcohols, phenols and ethers, with all 15 conversions solved correctly.

Week 3

Aldehydes, Ketones, Carboxylic Acids and Organic Compounds Containing Nitrogen

  • Describe the mechanism of nucleophilic addition to carbonyl compounds and rank aldehydes and ketones by reactivity toward HCN, bisulphite and Grignard reagents.

  • Write balanced equations for aldol condensation, Cannizzaro reaction, Clemmensen reduction, Wolff–Kishner reduction, haloform reaction and the Tollens, Fehling and Schiff tests.

  • Compare the acidity of substituted benzoic acids and aliphatic carboxylic acids, and outline HVZ reaction, decarboxylation and esterification.

  • Distinguish primary, secondary and tertiary amines by Hinsberg test and carbylamine test, and rank them by basicity in aqueous solution.

  • Outline diazonium salt preparation and four coupling or substitution reactions used to synthesise substituted aromatic compounds.

Your checkpoint

A reaction-scheme flow chart for aldehydes, ketones, acids and amines plus 20 conversion problems solved with reagents written above each arrow.

Week 4

p-Block Elements

  • Summarise group trends in atomic radius, ionisation enthalpy, electronegativity and oxidation states across groups 15 to 18.

  • Explain the anomalous behaviour of nitrogen, oxygen, fluorine and phosphorus in terms of small size, high electronegativity and absence of d orbitals.

  • Draw structures and compare the acidic strengths of the oxoacids of phosphorus, sulphur and chlorine.

  • Describe the preparation of nitric acid by Ostwald process and sulphuric acid by contact process, listing conditions and three major uses of each.

  • Explain the bonding and shape of interhalogen compounds and noble gas fluorides, and account for the inert-pair effect.

Your checkpoint

A p-block comparison table of 25 species (oxoacids, interhalogens, noble-gas compounds) with shape, hybridisation and one key reaction.

Week 5

Solid State and Solutions & Electrochemistry

  • Calculate packing efficiency, unit-cell dimensions and density for simple cubic, body-centred and face-centred cubic lattices.

  • Distinguish Schottky and Frenkel defects and explain how doping changes conductivity in intrinsic and extrinsic semiconductors.

  • Apply Raoult's law and van't Hoff factor to calculate vapour pressure lowering, boiling-point elevation, freezing-point depression and osmotic pressure for electrolyte solutions.

  • Use the Nernst equation to calculate electrode potential and cell emf for concentration cells and for cells with gas electrodes.

  • Apply Kohlrausch's law, Faraday's laws and conductance relationships to solve numerical problems on electrolysis and molar conductivity.

Your checkpoint

A numerical problem set of 20 questions on solid state, solutions and electrochemistry, with a formula sheet and at least 80% accuracy.

Week 6

Chemical Kinetics & Surface Chemistry

  • Determine order and rate constant from integrated rate laws for zero-, first- and second-order reactions, including graphical methods.

  • Apply the Arrhenius equation to calculate activation energy from two rate constants, and explain collision theory and the effect of a catalyst.

  • Distinguish physisorption from chemisorption by enthalpy, reversibility and multilayer formation, and apply the Freundlich isotherm.

  • Classify colloids, explain the Tyndall effect, Brownian movement and electrophoresis, and apply the Hardy–Schulze rule to compare coagulating power.

  • Describe the preparation and purification of colloids and the action of emulsifiers and surfactants.

Your checkpoint

A one-page kinetics and surface-chemistry formula sheet plus 15 numericals on rate laws, half-life, Arrhenius and isotherms solved correctly.

Week 7

General Principles and Processes of Isolation of Elements & Biomolecules, Polymers and Chemistry in Everyday Life

  • Sequence the metallurgical steps of concentration, roasting, calcination, reduction and refining, and choose the correct step for a named ore.

  • Interpret an Ellingham diagram to decide the temperature range for reduction of an oxide by carbon or aluminium.

  • Explain van Arkel de Boer, Mond process, zone refining and electrolytic refining with the metal each is used for.

  • Classify carbohydrates, proteins, enzymes, vitamins and nucleic acids, and describe the primary and secondary structure of proteins.

  • Distinguish addition and condensation polymers, thermoplastic and thermosetting polymers, and explain the cleansing action of soaps and detergents.

Your checkpoint

A two-page metallurgy flowchart plus a biomolecules and polymers glossary of 40 terms with one example each.

Week 8

Solid State and Solutions & Electrochemistry & Chemical Kinetics & Surface Chemistry & General Principles and Processes of Isolation of Elements & p-Block Elements & d- and f-Block Elements and Coordination Compounds & Haloalkanes, Haloarenes, Alcohols, Phenols and Ethers & Aldehydes, Ketones, Carboxylic Acids and Organic Compounds Containing Nitrogen & Biomolecules, Polymers and Chemistry in Everyday Life

  • Complete one full-length mock paper under timed conditions and mark it against the answer key.

  • Build an error log classifying every mistake as conceptual, calculation, equation-balancing or recall.

  • Re-teach the three weakest topics from the error log using the week 1–7 summary sheets.

  • Rehearse the 20 highest-frequency named reactions and 15 numerical formulas from memory.

Your checkpoint

A timed mock paper attempted in full, an error log with at least 15 entries, and a scored mock result of 70% or above.

Milestones

Week 2: Score 80% or above on a 20-question mixed quiz on domains 7 and 8, and name 10 coordination compounds and 10 haloalkanes without notes.

Week 4: Complete 20 named organic conversions from domains 8 and 9 and a 15-question p-block quiz at 75% accuracy.

Week 6: Solve 15 numericals spanning solid state, solutions, electrochemistry and kinetics within 45 minutes at 75% accuracy.

Week 8: Finish a full-length timed mock at 70% or above, with the error log reviewed and the three weakest topics re-tested.