Advanced Level Chemistry – Quick Reference Notes

Unit 1 – Atomic Structure

• Matter = anything with mass + occupies space → ~118 known elements → ~100 found naturally.
• Historical ideas
– Empedocles: 4 elements.
– Democritus: atomos (indivisible).
– Dalton (1808) ⮕ Golf-ball model; 4 postulates (atoms, identity, conservation, fixed ratios).

Discovery of sub-atomic particles

• Cathode rays → electrons (J.J. Thomson 1897) → e/m=1.76×108C g1e/m =1.76\times10^{8}\,\text{C g}^{-1}.
• Millikan oil-drop (1909) → q<em>e=1.602×1019Cq<em>e =1.602\times10^{-19}\,\text{C}; m</em>e=9.11×1028gm</em>e =9.11\times10^{-28}\,\text{g}.
• Canal (anode) rays → protons, m<em>p=1.673×1024gm<em>p =1.673\times10^{-24}\,\text{g}. • Rutherford gold-foil → nuclear model; nucleus tiny, +vely charged. • Chadwick (1932) → neutron, m</em>n=1.675×1024gm</em>n =1.675\times10^{-24}\,\text{g}, q=0q=0.

Atomic number Z, mass number A

Z=p=eZ=p=e (neutral atom).
A=Z+nA=Z+n.
• Isotopes: same Z, different A.
• Unified amu 1u=112M(12C)=1.66054×1024g1\,\text{u}= \dfrac1{12}M(^{12}\text C)=1.66054\times10^{-24}\,\text g.
• Average atomic mass Mˉ=(m<em>ix</em>i)\bar{M}=\sum (m<em>i\,x</em>i).

Electromagnetic radiation

• Wave parameters: c=λνc=\lambda\nu; E=hνE=h\nu where h=6.626×1034J sh=6.626\times10^{-34}\,\text{J s}.
• Einstein photon; de Broglie matter wave λ=hmv\lambda=\dfrac{h}{mv}.

Hydrogen spectrum & Bohr model

• Electrons occupy orbits n=1,2n=1,2\dots; energy quantised → line spectra (Lyman, Balmer, Paschen…).

Quantum numbers

• n (principal), l (0 → n–1; s p d f), m<em>l=l..+lm<em>l=-l..+l, m</em>s=±12m</em>s=\pm\tfrac12.
• Subshell degeneracy; total orbitals per shell n2n^2.

Electron configurations

• Aufbau order (1s,2s,2p,3s,3p,4s,3d…).
• Pauli Exclusion: max 2e⁻ per orbital opposite spin.
• Hund: degenerate orbitals singly with parallel spins first.
• Condensed form e.g. [Ne]3s1[\text{Ne}]3s^1.
• Cr, Cu anomalies: [Ar]3d54s1[Ar]3d^54s^1, [Ar]3d104s1[Ar]3d^{10}4s^1.

Periodic Table building

• Groups 1–18 (IUPAC).
• Blocks: s (2 columns), p (6), d (10), f (14).

Periodic trends (s & p blocks)

• Atomic radii ↓ across (Z_eff ↑), ↑ down (n ↑).
• Ionisation energy ↑ across, ↓ down; big jumps after core e⁻ removal.
• Electron gain (affinity) most exothermic for halogens; less favourable down group.
• Electronegativity (Pauling) ↑ across, ↓ down.


Unit 2 – Structure & Bonding

Types of bonds

• Ionic: electrostatic M⁺ … X⁻, lattice E.
• Covalent: shared pair; octet rule; σ,  π\sigma,\;\pi bonds.
• Dative (coordinate): both electrons donated e.g. \ce{NH3->BF3}.
• Metallic: cations in e⁻ sea; strength ↑ with charge density.

Lewis structures

• Procedure: count valence e⁻, place pairs, satisfy octet/duet, formal charges FC=V(L+B)FC=V-(L+B) minimise.
• Resonance ↔ equivalent contributors; hybrid ↓E.

VSEPR geometries (AXmEn)

• 2 e-pairs: linear 180° (BeCl2, CO2).
• 3: trig-planar 120° (BF3); AX2E bent <120° (SO2).
• 4: tetrahedral 109.5° (CH4); AX3E trig pyramidal (NH3); AX2E2 bent 104.5° (H2O).
• 5: trig bipyramidal (PCl5); see-saw (SCl4); T-shape (ICl3); linear (XeF2).
• 6: octahedral (SF6); square pyramidal (XeOF4); square planar (XeF4).

Hybridisation

• sp (linear), sp2 (trig planar), sp3 (tetrahedral).
• Multiple bonds: one σ\sigma + one/two π\pi.

Inter-molecular forces

• Ion-dipole, H-bond (FON), dipole-dipole, London (dispersion), dipole-induced, ion-induced.
• Boiling/melting relate to IMF & molar mass (n-pentane vs neopentane).


Unit 3 – Chemical Calculations

Oxidation number rules

• Free element 0; Group1 +1; Group2 +2; F −1; H +1 (−1 in hydrides); O −2 (−1 in peroxides, −½ in superoxides, +2 in OF2).
• Sum in molecule 0, in ion = charge.

Redox concepts

• Oxidation = loss e⁻ (ON ↑), Reduction = gain e⁻ (ON ↓).
• Balancing: inspection; oxidation-number; half-reaction (acid/base media).

Formulae & composition

• Empirical from %: convert to mol, divide by smallest, scale ↓.
• Molecular: n=M<em>rM</em>emp\text{n}=\dfrac{M<em>r}{M</em>{emp}}.
• Mass %, ppm, ppb; ppm=mass solutemass solution106\text{ppm}=\dfrac{\text{mass solute}}{\text{mass solution}}10^{6}.
• Molality m=n<em>solutekg</em>solventm=\dfrac{n<em>{solute}}{kg</em>{solvent}}.
• Molarity c=nV(dm3)c=\dfrac{n}{V(\text{dm}^3)}.

Stoichiometry

• Limiting reagent concept.
• Gravimetric & titrimetric calculations.

Solution prep

• Weigh solid → dissolve → volumetric flask.
• Dilution M<em>1V</em>1=M<em>2V</em>2M<em>1V</em>1=M<em>2V</em>2.


Unit 6 – Chemistry of s, p & d Blocks

Group 1 (Alkali)

• Valence ns1ns^1; low density, soft, MP ↓ down group.
• Reactivity ↑ down; with \ce{H2O}: 2M+2H2O2MOH+H22M+2H2O→2MOH+H2 (Li slow, Cs explosive).
• O₂: 4M+O22M2O4M+O2→2M2O; K/Rb/Cs form superoxides MO2MO2.
• Salts: all soluble; LiF, Li2CO3 sparingly.
• Flame colours: Li red, Na yellow, K lilac.

Group 2 (Alkaline earth)

• Valence ns2ns^2; harder, MP high.
• Water: Be none; Mg hot water; Ca→Ba vigorous.
• Thermal stability of carbonates ↑ down; nitrates give M(NO<em>3)</em>2MO+NO2+O2M(NO<em>3)</em>2 → MO+NO2+O2.
• Flame: Ca orange-red, Sr crimson, Ba apple-green.

p-Block highlights

• Group13: B non-metal, Al amphoteric; Al<em>2O</em>3Al<em>2O</em>3 amphoteric; AlCl<em>3AlCl<em>3 dimeric Al</em>2Cl<em>6Al</em>2Cl<em>6. • Group14: C allotropes (diamond sp3, graphite sp2, π\pi deloc), fullerenes; COCO triple bond; CO</em>2CO</em>2 linear.
• Group15: N₂ inert (triple 942 kJ mol⁻¹); variable ox states −3→+5; NH<em>3NH<em>3 basic ligand; HNO3HNO3 strong oxidiser. • Group16: O₂/ O₃ oxidants; S allotropes S</em>8S</em>8; acid–base nature of oxides shift basic→acidic across period; hydrides acidity ↑ down (HF weak due H-bond).
• Group17: Halogens oxidising strength F2>Cl2>Br2>I2; HX acid strength ↑ down; ClOClO^- series (-ite, –ate); KMnO<em>4KMnO<em>4 tests (purple→colourless). • Group18: Noble gases; Xe forms XeF</em>2,XeF<em>4,XeO</em>3,XeF</em>2, XeF<em>4, XeO</em>3, etc.

d-Block (Transition)

• Definition: incomplete d in atom or common ion; Sc (d¹) – Zn (d¹⁰).
• Properties: variable ox states (+2 prevalent), coloured complexes, catalytic, magnetic, form alloys.
• Electronic anomalies Cr (3d⁵4s¹), Cu (3d¹⁰4s¹).
• Complex nomenclature: ligand names (ammine, aqua, chlorido); e.g. [Fe(CN)<em>6]3[Fe(CN)<em>6]^{3-} = hexacyanidoferrate(III). • Colour factors: metal, ox state, ligand field. • Qualitative tests: – \ce{Fe^{2+}} + \ce{[Fe(CN)6]^{3-}} → Turnbull blue.
– \ce{Fe^{3+}} + \ce{SCN^-} → blood-red [Fe(SCN)]2+[Fe(SCN)]^{2+}.
– \ce{Cr^{3+}} + \ce{H2O2/OH^-} → yellow CrO42CrO_4^{2-}.


Key Equations (selection)

c=λνc=\lambda\nu; E=hνE=h\nu; λ=hmv\lambda=\dfrac{h}{mv}
• Atomic mass Mˉ=m<em>ix</em>i\bar{M}=\sum m<em>ix</em>i.
• Molality m=nkgm=\dfrac{n}{kg}; Molarity M=nV<em>dm3M=\dfrac{n}{V<em>{dm^3}}. • Ideal dilution M</em>1V<em>1=M</em>2V2M</em>1V<em>1=M</em>2V_2.
• Gibbs ΔG=ΔHTΔS\Delta G=\Delta H-T\Delta S.


Ethical / Practical Notes

• H₂S, CO, Cl₂ highly toxic → lab ventilation.
• KMnO₄ stains; concentrated H<em>2SO</em>4H<em>2SO</em>4 dehydrating agent.
• Transition-metal waste can be environmentally harmful; proper disposal.