Reference
The 49 reactions and formulas MHT-CET Chemistry actually tests
One page, grouped by chapter in strand order. The Calculate chapters carry their formulas, the Reactions chapters their named reactions and reagents, the Recall chapters their tables. At about 40 seconds a Chemistry question, a reaction you have to work out in the hall is time Physics does not get.
- reactions and formulas
- 49
- chapters covered
- 20
- a question, Paper II average
- 0.9 min
- papers of PYQs behind it
- 42
How to use this page
- First read: cover-to-cover, marking every line you don’t already know cold. The groups follow the strategy strands — Calculate, then Reactions, then Recall.
- Learn reactions both ways: the paper asks for the product from a reagent AND the reagent from a product. Clemmensen and Wolff–Kishner give the same product from opposite conditions; Finkelstein and Swarts differ in one halide. The look-alike is always an option.
- Active recall: cover the right-hand side, read only the NAME, and write the reaction or formula from memory. Anything you miss goes on tomorrow’s list. Each chapter header links to its playbook, which is where you find out how the paper uses it.
Solutions and Colligative Properties
PlaybookColligative properties
ΔT_b = i·K_b·m ΔT_f = i·K_f·m π = i·C·R·T (p° − p)/p° = x₂
- m = molality
- C = molarity
- i = van't Hoff factor
Note:i = 2 for NaCl, 3 for CaCl₂, 4 for AlCl₃ (full dissociation).
Henry's law
C = K_H · p
- C = solubility of the gas
- p = its partial pressure
Solid State
PlaybookDensity of a unit cell
ρ = z·M / (a³·N_A)
- z = 1 (sc), 2 (bcc), 4 (fcc)
- a in cm
Radius and edge
sc: r = a/2 bcc: r = √3·a/4 fcc: r = √2·a/4
- a = edge length
Packing and voids
sc 52.4% bcc 68% fcc/hcp 74% n atoms → n octahedral, 2n tetrahedral voids
Chemical Kinetics
PlaybookFirst-order kinetics
k = (2.303/t)·log(a/(a − x)) t½ = 0.693/k
- a = initial amount
- x = amount reacted
Note:log 2 = 0.301, log 3 = 0.477, log 5 = 0.699 — no calculator.
Zero-order kinetics
[A] = [A]₀ − kt t½ = [A]₀ / 2k
Arrhenius
log(k₂/k₁) = (Eₐ / 2.303R)·(1/T₁ − 1/T₂)
- Eₐ = activation energy
Ionic Equilibria
PlaybookpH
pH = −log[H⁺] pH + pOH = 14 (25 °C)
Weak electrolytes
α = √(K/c) [H⁺] = √(Ka·c)
- α = degree of dissociation
Buffer
pH = pKa + log([salt]/[acid])
Solubility product
AB: s² AB₂: 4s³ A₂B₃: 108s⁵
- s = molar solubility
Chemical Thermodynamics and Energetics
PlaybookFirst law
ΔU = q + w w = −P_ext·ΔV 1 dm³ bar = 100 J
- Work done ON the system is positive
ΔH and ΔU
ΔH = ΔU + Δn_g·R·T
- Δn_g = gas moles of products − reactants
Gibbs energy
ΔG = ΔH − TΔS ΔG° = −2.303RT·log K equilibrium T = ΔH/ΔS
Electrochemistry
PlaybookCell potential and energy
E°cell = E°cathode − E°anode ΔG° = −n·F·E°
- reduction potentials for both
Nernst equation (25 °C)
E = E° − (0.0592/n)·log Q
- n = electrons transferred
Conductivity
κ = cell constant / R Λm = 1000·κ / c α = Λm / Λ°m
- Λm in S cm² mol⁻¹
Faraday's law
m = (M / n·F)·I·t 1 F = 96500 C
Structure of Atom
PlaybookBohr model
r = 0.529·n²/Z Å E = −13.6·Z²/n² eV
Radiation and matter waves
E = h·ν = h·c/λ λ = h/(m·v)
Some Basic Concepts of Chemistry
PlaybookThe mole
n = m/M = N/N_A = V/22.4 dm³ (gas at STP)
- N_A = 6.022 × 10²³
Concentration
molarity = mol / L solution molality = mol / kg solvent
Alcohols, Phenols and Ethers
PlaybookLucas test
ZnCl₂/conc. HCl: 3° turbid at once · 2° in minutes · 1° not at room temperature
Phenol named reactions
Reimer–Tiemann: phenol + CHCl₃/NaOH → salicylaldehyde Kolbe: sodium phenoxide + CO₂ → salicylic acid
Williamson ether synthesis
R–O⁻Na⁺ + R′–X → R–O–R′
- R′–X should be primary
Aldehydes, Ketones and Carboxylic Acids
PlaybookMaking aldehydes
Rosenmund: RCOCl + H₂ (Pd/BaSO₄) → RCHO Stephen: RCN + SnCl₂/HCl → RCHO Etard: toluene + CrO₂Cl₂ → benzaldehyde
C=O to CH₂
Clemmensen: Zn–Hg / conc. HCl Wolff–Kishner: NH₂NH₂ / KOH
Tests
Tollens' → silver mirror (aldehydes) Fehling's → red Cu₂O iodoform: CH₃CO– or CH₃CH(OH)–
Aldol and Cannizzaro
Aldol: needs α-H Cannizzaro: no α-H (HCHO, C₆H₅CHO) → alcohol + acid salt
Amines
PlaybookBasicity in water
(CH₃)₂NH > CH₃NH₂ > (CH₃)₃N > NH₃ > C₆H₅NH₂
Hofmann bromamide
RCONH₂ + Br₂ + 4NaOH → RNH₂ (one carbon fewer)
Diazonium salts
C₆H₅NH₂ + NaNO₂/HCl (273 K) → C₆H₅N₂⁺Cl⁻ → phenol (H₂O, Δ) · C₆H₅Cl (CuCl, Sandmeyer)
Halogen Derivatives of Alkanes
PlaybookHalide exchange
Finkelstein: RCl/RBr + NaI (acetone) → RI Swarts: RCl + AgF → RF
Coupling
Wurtz: 2RX + 2Na → R–R Fittig: 2ArX + 2Na → Ar–Ar Wurtz–Fittig: ArX + RX + 2Na → Ar–R
Substitution against elimination
aq. KOH → alcohol alc. KOH → alkene (Saytzeff: more substituted) 3° SN1, 1° SN2
Aromatic Compounds
PlaybookAromaticity
planar · cyclic · conjugated · (4n + 2) π electrons
Directing groups
o/p: –OH –NH₂ –R –X m: –NO₂ –CN –CHO –COOH
Alkanes
PlaybookDecarboxylation
RCOONa + NaOH (CaO, Δ) → R–H + Na₂CO₃
- one carbon fewer
Grignard to alkane
RMgX + H₂O → R–H
Biomolecules
PlaybookGlycosidic linkages
sucrose α1–β2 (non-reducing) · maltose α1–4 · lactose β1–4 · cellulose β1–4 · starch α1–4 + α1–6
Nucleic acid bases
DNA: A G C T + deoxyribose RNA: A G C U + ribose
Coordination Compounds
PlaybookEffective atomic number
EAN = Z − oxidation state + 2 × coordination number
Denticity
mono: NH₃ H₂O Cl⁻ CN⁻ bi: en ox²⁻ hexa: EDTA⁴⁻
Introduction to Polymer Chemistry
PlaybookMonomers
nylon 6,6: hexamethylenediamine + adipic acid · nylon 6: caprolactam · Buna-S: butadiene + styrene · Buna-N: butadiene + acrylonitrile · terylene: ethylene glycol + terephthalic acid · bakelite: phenol + formaldehyde
Transition and Inner Transition Elements
PlaybookSpin-only magnetic moment
μ = √(n(n + 2)) BM n = 1→1.73 · 2→2.83 · 3→3.87 · 4→4.90 · 5→5.92
- n = unpaired electrons
Chemical Bonding and Molecular Structure
PlaybookBond order
bond order = (bonding − antibonding electrons) / 2 N₂ 3 · O₂ 2 · O₂⁻ 1.5 · O₂²⁻ 1
VSEPR
steric number 2 linear · 3 trigonal planar · 4 tetrahedral · 5 trigonal bipyramidal · 6 octahedral
- lone pairs bend the shape
Surface Chemistry
PlaybookHardy–Schulze rule
negative sol: Al³⁺ > Ba²⁺ > Na⁺ positive sol: [Fe(CN)₆]⁴⁻ > SO₄²⁻ > Cl⁻
- the ion opposite in charge to the sol coagulates it
Why plain text (not typeset)
Everything on this page is plain text plus unicode (ρ = z·M/(a³·N_A), RCOCl + H₂ → RCHO, μ = √(n(n + 2))). Plain text means the page loads instantly, copies cleanly into your own notes, and reads correctly to a screen reader symbol by symbol. Full typesetting is reserved for the teaching notes, where you are solving rather than revising.