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Who discovered the electron and how?
J.J. Thomson (1897) — cathode ray tube; beam deflected by electric/magnetic fields proving negative subatomic particles exist
Who discovered the nucleus and how?
Rutherford (1911) — gold foil experiment; most alpha particles passed through, ~1/8000 bounced back → small dense positive nucleus
What did Bohr contribute?
Electrons orbit nucleus in fixed energy shells; electrons emit/absorb specific energy as photons when changing shells — explains line spectra
What did Chadwick discover?
Neutron (1932) — bombarded beryllium with alpha particles; detected massive uncharged radiation
What was unknown at the time of Bohr's model (1913)?
Neutrons — discovered by Chadwick in 1932
Number of emission lines when electron excited to shell n
n(n−1)/2. e.g. excited to n=4: 4×3/2 = 6 lines
Which transition gives shortest wavelength emission?
Largest energy drop — e.g. n=4 → n=1 (more energy = shorter wavelength)
Which transition gives longest wavelength in hydrogen visible spectrum?
n=3 → n=2 (smallest energy gap in visible range; red line)
Energy gap trend between shells
Gets smaller as shells are further from nucleus
Ion notation format
Mass number top-left, atomic number bottom-left, charge top-right: e.g. ²³⁸₉₂U⁴⁺
For a cation, how many electrons?
Protons minus charge. e.g. K⁺ (Z=19): 19−1 = 18 electrons
For an anion, how many electrons?
Protons plus charge magnitude. e.g. O²⁻ (Z=8): 8+2 = 10 electrons
Electron configuration of K (Z=19)
2, 8, 8, 1
Electron configuration of Ca (Z=20)
2, 8, 8, 2
Electron configuration of Cl (Z=17)
2, 8, 7
Electron configuration of Ar (Z=18)
2, 8, 8
What are isotopes?
Same element (same protons), different neutrons → different mass number. Same chemical properties, different physical properties
Atomic radius trend across a period
Decreases left to right — same number of shells but increasing nuclear charge pulls electrons closer
Atomic radius trend down a group
Increases — extra shell added, valence electrons further from nucleus with more shielding
Melting point trend across Period 3
Na→Mg→Al increases (stronger metallic bonding); Si highest (covalent network); P, S, Cl, Ar drop sharply (covalent molecular — weak dispersion forces only)
Melting point trend down Group 1
Decreases — atomic radius increases, metallic bond weakens
Melting point trend down Group 17
Increases — larger molecules, more electrons, stronger dispersion forces between molecules
Melting point trend down Group 18
Increases — larger atoms, more electrons, stronger dispersion forces
Valency trend across Period 3
Na=1, Mg=2, Al=3, Si=4, P=3, S=2, Cl=1, Ar=0
Which Period 3 element has the highest melting point and why?
Si — covalent network solid; all covalent bonds throughout the lattice must be broken to melt it
Why do P, S, Cl, Ar have much lower melting points than Si?
They are covalent molecular — only weak dispersion forces between molecules need to be overcome, not strong covalent bonds
Which Group 2 element has the highest melting point?
Beryllium (Be) — smallest atomic radius, strongest metallic bonding
How to identify a metallic substance from properties
Conducts electricity in both solid AND liquid state; malleable; generally high melting point
How to identify an ionic substance from properties
Does NOT conduct as solid; DOES conduct when molten or dissolved; high melting point; hard and brittle
How to identify a covalent molecular substance from properties
Low melting point; does not conduct in solid or liquid state; exists as discrete molecules
How to identify a covalent network substance from properties
Very high melting point; extremely hard; does not conduct electricity (except graphite)
Metal + non-metal → what bond type?
Ionic
Non-metal + non-metal → what bond type?
Covalent
Metal alone or two metals → what bond type?
Metallic
Does SiO₂ conduct electricity?
No — covalent network solid; no mobile charged particles
Does graphite conduct electricity?
Yes — one delocalised electron per carbon atom free to move between layers
Ammonium ion
NH₄⁺
Hydroxide ion
OH⁻
Nitrate ion
NO₃⁻
Carbonate ion
CO₃²⁻
Sulfate ion
SO₄²⁻
Phosphate ion
PO₄³⁻
Permanganate ion
MnO₄⁻
Dichromate ion
Cr₂O₇²⁻
Chromate ion
CrO₄²⁻
Oxalate ion
C₂O₄²⁻
Cyanide ion
CN⁻
Hydrogen carbonate (bicarbonate) ion
HCO₃⁻
Acetate (ethanoate) ion
CH₃COO⁻
Thiosulfate ion
S₂O₃²⁻
Iron(II) and Iron(III) charges
Fe²⁺ and Fe³⁺
Copper(I) and Copper(II) charges
Cu⁺ and Cu²⁺
Lead(II) charge
Pb²⁺
Silver ion
Ag⁺
Zinc ion
Zn²⁺
Fe³⁺ colour in solution
Pale brown/yellow
Cu²⁺ colour in solution
Blue
Fe²⁺ colour in solution
Pale green
Acid + carbonate → products
Salt + water + CO₂(g)
Acid + metal → products
Salt + H₂(g)
Acid + base/metal hydroxide → products
Salt + water
Silver carbonate + nitric acid — net ionic equation
Ag₂CO₃(s) + 2H⁺(aq) → 2Ag⁺(aq) + H₂O(l) + CO₂(g)
Copper sulfate + excess KOH — observation
Blue precipitate of Cu(OH)₂ forms
Zinc + dilute H₂SO₄ — observation
Zinc dissolves; bubbles of hydrogen gas produced
Magnesium + hydrochloric acid — ionic equation
Mg(s) + 2H⁺(aq) → Mg²⁺(aq) + H₂(g)
Silver chloride precipitate colour
White
Silver bromide precipitate colour
Cream/pale yellow
Silver iodide precipitate colour
Yellow
Copper(II) hydroxide precipitate colour
Blue
Iron(III) hydroxide precipitate colour
Brown/rust
Iron(II) hydroxide precipitate colour
Green
Mole definition
6.022×10²³ particles (Avogadro's number)
n = m/M
moles = mass ÷ molar mass
n = V/22.71
moles of gas = volume in litres ÷ 22.71 at STP (0°C, 100 kPa)
PV = nRT — what is R?
8.314 J mol⁻¹ K⁻¹ (use P in Pa, V in m³, T in K)
How to convert °C to K
Add 273
Empirical formula method from % composition
Assume 100 g sample; convert % to g; divide each by molar mass to get moles; divide all by smallest value; round to whole number ratio
Molecular formula from empirical formula
Divide given molar mass by empirical formula mass; multiply all subscripts by that factor
Percentage composition formula
(mass of element in one mole ÷ molar mass of compound) × 100
General formula — alkanes
CₙH₂ₙ₊₂
General formula — alkenes
CₙH₂ₙ
General formula — cycloalkanes
CₙH₂ₙ
General formula — cycloalkenes
CₙH₂ₙ₋₂
What makes a hydrocarbon saturated?
Contains only single C–C bonds (alkanes, cycloalkanes)
What makes a hydrocarbon unsaturated?
Contains at least one C=C double bond (alkenes, cycloalkenes) or aromatic ring (benzene)
IUPAC naming — which end do you number from?
The end closest to the first branch or double bond
How to name a halogen substituent in IUPAC
Prefix: fluoro-, chloro-, bromo-, iodo- with position number; listed alphabetically before carbon chain name
Structural isomers definition
Same molecular formula, different structural arrangement of atoms
Geometric (cis/trans) isomers — when are they possible?
Only when each carbon of the C=C has two DIFFERENT groups attached
cis isomer definition
Same priority groups on the same side of the double bond
trans isomer definition
Same priority groups on opposite sides of the double bond
Alkene + Br₂ (no UV, no catalyst) — reaction type and observation
Addition reaction; bromine water/liquid bromine decolourises
Alkane + Cl₂ or Br₂ — conditions required
UV light (free radical substitution)
Benzene + halogen — reaction type and conditions
Electrophilic substitution; requires AlX₃ halogen carrier catalyst
Does benzene decolourise bromine water?
No — benzene does not undergo addition reactions; substitution only
Test to distinguish an alkene from a cycloalkane
Add bromine water — alkene decolourises it; cycloalkane does not react (no UV light present)
Cyclohexene + Br₂(l) no UV — product
1,2-dibromocyclohexane (addition across the double bond)
Benzene + I₂ + AlI₃ — organic product
Iodobenzene (substitution; HI also produced as byproduct)
Complete combustion of a hydrocarbon — products
CO₂(g) and H₂O(g) only (requires excess O₂)
Incomplete combustion of a hydrocarbon — products
CO and/or C(s) soot and H₂O (limited O₂)