CBSE Board Exam 2026–27 · Class 12 Chemistry

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Reference Sheet

Solutions & Chemical Kinetics

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10
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01

Unit I

The Chemistry of Solutions

Chemistry solutions
CONCENTRATION EXPRESSIONS
Mass%, Molarity, Molality, Normality & More
Vapour pressure laboratory

Raoult's Law & Vapour Pressure

Raoult's Law describes how the vapour pressure of an ideal solution depends on the mole fractions of its components. Solutions may exhibit positive or negative deviations from ideality.

p_A = p°_A × χ_A p_total = p°_A·χ_A + p°_B·χ_B (p° – p)/p° = χ_B [RLVP]

Ideal: ΔH_mix = 0, ΔV_mix = 0
+ve deviation: A–B weaker than A–A & B–B
–ve deviation: A–B stronger than A–A & B–B

Dissolved gas bubbles

Henry's Law — Gas Solubility

Henry's Law quantifies how gas dissolves in a liquid under pressure. Higher K_H means lower solubility at a given pressure. Gas solubility decreases with temperature as K_H increases.

p = K_H × χ K_H = p / χ S₁/S₂ = p₁/p₂ [at two pressures]

Applications: carbonated beverages, scuba diving physiology, dissolved oxygen in water bodies.

Colligative Properties

Depend Only on Number of Particles

Osmosis membrane
VAN'T HOFF FACTOR (i)
Dissociation · Association · Modified Colligative Formulas
Salt crystals solubility

Solubility Product (Ksp)

The solubility product links molar solubility to equilibrium concentrations of ions. Different ionic stoichiometries yield different expressions.

AB type: Ksp = S² AB₂ type: Ksp = 4S³ A₂B₃ type: Ksp = 108S⁵ A₃B₂ type: Ksp = 108S⁵
Distillation azeotrope

Azeotropes

Azeotropes are constant-boiling mixtures that cannot be separated by simple distillation. Their type is linked to the nature of deviation from Raoult's Law.

Minimum Boiling Azeotrope: +ve deviation (e.g., EtOH–H₂O 95.5%) BP < both components Maximum Boiling Azeotrope: –ve deviation (e.g., HNO₃–H₂O 68%) BP > both components
02

Unit II

Chemical Kinetics

Reaction kinetics

Rate Laws & Reaction Orders

From zero-order flat lines to exponential first-order decay — master every integrated rate equation and half-life formula.

Integrated Rate Equations
Zero Order
First Order
Second Order
Pseudo First Order
nth Order
ZERO ORDER
Zero Order Integrated Law
Rate = k[A]⁰ = k (constant) [A] = [A]₀ – kt k = ([A]₀ – [A]) / t t₁/₂ = [A]₀ / 2k ← depends on [A]₀ t_complete = [A]₀ / k ← time for complete reaction Graph: [A] vs t → straight line, slope = –k

Units of k: mol L⁻¹ s⁻¹ (M·s⁻¹). Rate is constant regardless of concentration.

FIRST ORDER
First Order Integrated Law
Rate = k[A] ln[A] = ln[A]₀ – kt [A] = [A]₀ · e^(–kt) k = (2.303/t) × log([A]₀/[A]) t₁/₂ = 0.693/k = ln2/k ← INDEPENDENT of [A]₀ After n half-lives: [A] = [A]₀ × (1/2)ⁿ Fraction remaining = (1/2)ⁿ Fraction decomposed = 1 – (1/2)ⁿ Key times: t₅₀% = 0.693/k t₇₅% = 2 × t₁/₂ t₉₀% = 2.303/k t₉₉% = 4.606/k t₉₉.₉% = 6.909/k Graphs: [A] vs t → exponential decay ln[A] vs t → slope = –k log[A] vs t → slope = –k/2.303

Units of k: s⁻¹. Most important order for CBSE — radioactivity, hydrolysis, inversions.

SECOND ORDER
Second Order Integrated Law
Type I: 2A → Products Rate = k[A]² 1/[A] = 1/[A]₀ + kt t₁/₂ = 1/(k[A]₀) ← depends on 1/[A]₀ Graph: 1/[A] vs t → slope = +k Type II: A + B → Products ([A]₀ ≠ [B]₀) k = [2.303/t([A]₀–[B]₀)] × log([B]₀[A]/[A]₀[B])

Units of k: L mol⁻¹ s⁻¹ (M⁻¹s⁻¹). Half-life inversely proportional to initial concentration.

PSEUDO FIRST ORDER
Pseudo First Order Reactions
For A + B → Products, where [B] >> [A]: Rate = k[A][B] ≈ k′[A] k′ = k[B] (pseudo first order rate constant) Example: CH₃COOC₂H₅ + H₂O → CH₃COOH + C₂H₅OH Rate = k[ester][H₂O] ≈ k′[ester] (since [H₂O] is in vast excess and stays constant)

The reaction behaves as first order because one reactant concentration remains effectively constant.

nth ORDER
General nth Order Formula
1/[A]^(n–1) – 1/[A]₀^(n–1) = (n–1)kt [n ≠ 1] t₁/₂ = (2^(n–1) – 1) / [(n–1) × k × [A]₀^(n–1)] t₁/₂ ∝ 1/[A]₀^(n–1) Summary: Zero: t₁/₂ ∝ [A]₀ k units: M·s⁻¹ First: t₁/₂ = const k units: s⁻¹ Second: t₁/₂ ∝ 1/[A]₀ k units: M⁻¹s⁻¹ nth: k units: M^(1–n)s⁻¹
1/T → log k → slope = –Eₐ/2.303R y-int = log A Arrhenius Plot: log k vs 1/T

Arrhenius Equation

k = A × e^(–Eₐ/RT) ln k = ln A – Eₐ/RT log k = log A – Eₐ/(2.303RT) Two-temperature form: log(k₂/k₁) = Eₐ(T₂–T₁) / (2.303·R·T₁T₂) Eₐ = –2.303R × slope (from graph)

The Arrhenius plot (log k vs 1/T) is a straight line. Its slope gives activation energy; the y-intercept gives the pre-exponential factor A. A catalyst lowers Eₐ without changing ΔH or equilibrium.

03

Quick Reference

Data Tables

Reference data tables
CONSTANTS, K_f / K_b, HALF-LIVES
All numerical data for CBSE numerical problems
TABLE 1 — Important Constants
ConstantSymbolValue
Universal Gas ConstantR8.314 J mol⁻¹ K⁻¹ = 0.0821 L·atm·mol⁻¹·K⁻¹ = 2 cal mol⁻¹ K⁻¹
Avogadro's NumberN_A6.022 × 10²³ mol⁻¹
Boltzmann Constantk_B1.38 × 10⁻²³ J K⁻¹
Planck's Constanth6.626 × 10⁻³⁴ J·s
Standard Atmosphere1 atm101325 Pa = 101.325 kPa
TABLE 2 — Cryoscopic & Ebullioscopic Constants
SolventK_f (K·kg·mol⁻¹)K_b (K·kg·mol⁻¹)T_f (°C)T_b (°C)
Water1.860.520100
Benzene5.122.535.580.1
Chloroform4.683.63–63.561.2
Acetic Acid3.903.0716.6118.1
Carbon Tetrachloride29.85.03–22.976.7
Camphor40.05.61178.4207.4
Cyclohexane20.02.796.580.7
Naphthalene6.980.2
Nitrobenzene7.05.245.7210.8
TABLE 3 — Integrated Rate Law Summary
OrderRate LawIntegrated Formt₁/₂Units of k
0k[A] = [A]₀ – kt[A]₀/2kM·s⁻¹
1k[A]ln[A] = ln[A]₀ – kt0.693/ks⁻¹
2k[A]²1/[A] = 1/[A]₀ + kt1/(k[A]₀)M⁻¹s⁻¹
nk[A]ⁿComplex(2^(n–1)–1)/[(n–1)k[A]₀^(n–1)]M^(1–n)s⁻¹
TABLE 4 — Van't Hoff Factor for Common Electrolytes
ElectrolyteTypeIonsTheoretical i (complete dissoc.)
NaCl1:12i = 2
CaCl₂1:23i = 3
Na₂SO₄2:13i = 3
AlCl₃1:34i = 4
Al₂(SO₄)₃2:35i = 5
CH₃COOHWeak acid1 < i < 2
GlucoseNon-electrolytei = 1
Acetic acid in benzeneAssociationi < 1
TABLE 5 — % Completion for First Order Reactions
% CompletionFraction RemainingFormula
50%1/2t = 0.693/k = t₁/₂
75%1/4t = 2 × t₁/₂
87.5%1/8t = 3 × t₁/₂
90%1/10t = 2.303/k
93.75%1/16t = 4 × t₁/₂
99%1/100t = 4.606/k
99.9%1/1000t = 6.909/k
04

Symbol Reference

Master Glossary

Memory Aids

Tips & Mnemonics

Formula Sheet Compiled by

Akshit Tyagi

Akshit Tyagi

Class 12 · CBSE Chemistry · 2026–27

This comprehensive formula sheet covers every major and minor formula from Solutions and Chemical Kinetics as per the CBSE 2026–27 syllabus — over 150 formulas, 7 quick-reference tables, symbol glossary, and 10 exam mnemonics. Designed to be your one-stop reference for board exam preparation.