1.11.1 Why we need a counting unit1.21.2 Moles of atoms inside a molecule or formula unit1.31.3 Molar mass1.41.4 The mass–mole relation1.52.1 Avogadro's hypothesis1.62.2 Comparing gases1.72.3 The working relations1.82.4 Notes1.93.1 What a balanced equation tells us1.103.2 Method1.114.1 Concept1.124.2 How to find it1.135.1 Types of formula1.145.2 Finding the empirical formula1.155.3 From empirical to molecular formula1.165.4 Combustion analysis1.176.1 Molarity1.186.2 Concentration of ions1.196.3 Dilution1.206.4 Final tips for the chapter2.1Lesson 1: Early atomic models — Thomson and Rutherford2.21.1 Thomson's atomic model (1897)2.31.2 Rutherford's gold foil experiment2.41.3 Postulates of Rutherford's atomic model (1911)2.52.1 Atomic emission (line) spectrum2.62.2 Bohr's atomic model (1913)2.72.3 The hydrogen spectrum explained2.82.4 Success of Bohr's model2.92.5 Shortcomings of Bohr's model2.10Lesson 3: The modern atomic theory2.113.1 Dual nature of the electron2.123.2 Heisenberg's uncertainty principle2.133.3 Wave-mechanical theory (Schrödinger, 1926)2.143.4 Electron cloud and orbital2.15Lesson 4: Quantum numbers2.164.1 Principal quantum number (n)2.174.2 Subsidiary quantum number (ℓ)2.184.3 Magnetic quantum number (mℓ)2.194.4 Spin quantum number (ms)2.204.5 Relations between n, sublevels, orbitals and electrons2.21Lesson 5: Distribution of electrons in the atom2.225.1 Pauli's exclusion principle2.235.2 Aufbau (building-up) principle2.245.3 Hund's rule2.255.4 Putting it together — rules checklist3.11.1 The basis of arrangement3.21.2 Description of the table3.31.3 The four blocks of the periodic table3.41.4 Types of elements3.51.5 Using the configuration to find position3.6Lesson 2: Atomic radius3.72.1 Definition3.82.2 Variation across a period (left to right)3.92.3 Variation down a group3.102.4 Ionic radius compared with atomic radius3.113.1 Ionization energy (ionization potential)3.123.2 Electron affinity3.133.3 Electronegativity3.143.4 Electron affinity versus electronegativity3.153.5 Summary of the trends (representative elements)3.164.1 Metals and non-metals3.174.2 Trends of metallic character3.184.3 Oxides: acidic, basic, amphoteric and neutral3.194.4 Acidic and basic character in the periodic table3.205.1 Concept3.215.2 Ionic compounds3.225.3 Covalent compounds3.235.4 Rules3.246.1 Definitions3.256.2 Behaviour of an agent according to its oxidation number3.266.3 Identifying redox reactions by oxidation numbers3.276.4 Ionic equations, spectator ions and half-reactions3.286.5 Balancing ionic redox equations (half-reaction method)3.296.6 Special types of redox reactions3.306.7 Final summary1.11.1 Why we need a counting unit1.21.2 Moles of atoms inside a molecule or formula unit1.31.3 Molar mass1.41.4 The mass–mole relation1.5Lesson 2: Molar volume of gases1.6Lesson 3: Chemical calculations from the balanced symbolic equation1.7Lesson 4: The limiting reactant1.8Lesson 5: Calculating chemical formulas1.9Lesson 6: Concentration of solutions2.1Lesson 1: Early atomic models — Thomson and Rutherford2.21.1 Thomson's atomic model (1897)2.31.2 Rutherford's gold foil experiment2.41.3 Postulates of Rutherford's atomic model (1911)2.52.1 Atomic emission (line) spectrum2.62.2 Bohr's atomic model (1913)2.72.3 The hydrogen spectrum explained2.82.4 Success of Bohr's model2.92.5 Shortcomings of Bohr's model2.10Lesson 3: The modern atomic theory2.11Lesson 4: Quantum numbers2.124.1 Principal quantum number (n)2.134.2 Subsidiary quantum number (ℓ)2.144.3 Magnetic quantum number (mℓ)2.154.4 Spin quantum number (ms)2.164.5 Relations between n, sublevels, orbitals and electrons2.174.6 Worked examples2.18Lesson 5: Distribution of electrons in the atom3.11.1 The basis of arrangement3.21.2 Description of the table3.31.3 The four blocks of the periodic table3.41.4 Types of elements3.51.5 Using the configuration to find position3.6Lesson 2: Atomic radius3.73.1 Ionization energy (ionization potential)3.83.2 Electron affinity3.93.3 Electronegativity3.103.4 Electron affinity versus electronegativity3.113.5 Summary of the trends (representative elements)3.12Lesson 4: Metallic and non-metallic character; acidic and basic properties3.13Lesson 5: Oxidation numbers3.146.1 Definitions3.156.2 Behaviour of an agent according to its oxidation number3.166.3 Identifying redox reactions by oxidation numbers3.176.4 Ionic equations, spectator ions and half-reactions3.186.5 Balancing ionic redox equations (half-reaction method)3.196.6 Special types of redox reactions3.206.7 Final summary| Comparison aspect | Main idea | Keywords |
|---|---|---|
| Early atomic models | Thomson and Rutherford | ThomsonRutherford |
| • | The atomic emission spectrum and Bohr’s atomic model | atomicemissionspectrumBohr |
| The modern atomic theory |
| dualnatureuncertaintyprinciple |
| • | Quantum numbers | Quantumnumbers |
| Distribution of electrons in the atom |
| PauliAufbauHund |
| Observation | Conclusion |
|---|---|
| Most alpha particles passed straight through the foil and produced flashes at the original position. |
|
| A very small fraction (about 1 in thousands) bounced back (was reflected) towards the source. | There is a part of the atom of very high density that occupies a very small space: the nucleus. |
|
The charge of the dense part (where most of the mass is concentrated) is positive, like the alpha particles, so it repels them. |
| Comparison aspect | Main idea | Keywords |
|---|---|---|
| The atom |
| extremelysmallsizecomplex |
| The nucleus |
| muchsmalleratomvast |
| The electrons |
| verysmallmassnegligible |
| Model | Year | Idea | Evidence/limit |
|---|---|---|---|
| Thomson | 1897 | Solid positive sphere with embedded electrons | Disproved by gold foil |
| Rutherford | 1911 |
|
|
| Quantum number | Symbol | What it describes |
|---|---|---|
| Principal | n | Distance of the electron from the nucleus (main energy level) |
| Subsidiary (secondary, azimuthal) | ℓ |
|
| Magnetic | mℓ |
|
| Spin | ms | The spin motion of the electron about its own axis |
| ℓ | 0 | 1 | 2 | 3 |
|---|---|---|---|---|
| Sublevel | s | p | d | f |
| n | ℓ | sublevel | mℓ values | orbitals |
|---|---|---|---|---|
| 1 | 0 | 1s | 0 | 1 |
| 2 | 0 | 2s | 0 | 1 |
| 2 | 1 | 2p | −1, 0, +1 | 3 |
| 3 | 0 | 3s | 0 | 1 |
| 3 | 1 | 3p | −1, 0, +1 | 3 |
| 3 | 2 | 3d | −2, −1, 0, +1, +2 | 5 |
| 4 | 0, 1, 2, 3 | 4s, 4p, 4d, 4f | … and for 4f: −3 … +3 | 1, 3, 5, 7 |
| Comparison aspect | Main idea | Keywords |
|---|---|---|
| • |
| numbersublevelsmainlevel |
| The number of orbitals in a main level = n2 (level 2 |
| |
| The number of orbitals in a sublevel = (2ℓ + 1) | p has 2(1) + 1 = 3 | |
| • | The maximum number of electrons in a main level = 2n2 (twice the orbitals) | maximumnumberelectronsmain |
| Maximum electrons in a sublevel = 2(2ℓ + 1) |
| explainstakes |
| Level | n | Sublevels (ℓ) | Orbitals | Max electrons |
|---|---|---|---|---|
| K | 1 | 1s | 1 | 2 |
| L | 2 | 2s, 2p | 1 + 3 = 4 | 8 |
| M | 3 | 3s, 3p, 3d | 1 + 3 + 5 = 9 | 18 |
| N | 4 | 4s, 4p, 4d, 4f | 1 + 3 + 5 + 7 = 16 | 32 |
| Comparison aspect | Main idea | Keywords |
|---|---|---|
| Worked example 4.1 — allowed values. |
| sublevelsorbitals |
| Worked example 4.2 — for n = 4 count everything. |
| SublevelsOrbitalsMaximumelectrons |
| Worked example 4.3 — check a set of quantum numbers. | n = 2, ℓ = 2, mℓ = 0, ms = +½. Invalid, because ℓ must be less than n (maximum n − 1 = 1). n = 3, ℓ = 1, mℓ = −1, ms = −½: valid (a 3p electron). | Invalidbecausemustless |
| Worked example 4.4 — identify the sublevel. |
| electronholdelectrons |
| Comparison aspect | Main idea | Keywords |
|---|---|---|
| Worked example 4.5 — find an error. | n = 2, ℓ = 1, mℓ = +2, ms = ½. mℓ must be between −1 and +1, so +2 is not allowed (it would need ℓ ≥ 2). | mustbetweenallowedwould |
| Worked example 4.6 — quantum numbers of the last electron. | Convention used: the p orbitals are filled in the order mℓ = −1, 0, +1, first singly with ms = +½, then pairing with ms = −½ in the same order (other textbooks may reverse the order; the key is to follow Hund’s rule consistently). | Conventionusedorbitalsfilled |
| Comparison aspect | Main idea | Keywords |
|---|---|---|
| Boron (₅B) |
| lastelectronfirst |
| Fluorine (₉F) |
| Electronsoccupypairslast |
| Sodium (₁₁Na) |
| lastelectron |
| Electron | n | ℓ | mℓ | ms |
|---|---|---|---|---|
| first | 3 | 0 | 0 | +½ |
| second | 3 | 0 | 0 | −½ |
| Comparison aspect | Main idea | Keywords |
|---|---|---|
| • | Worked example 5.1 (book examples) | Workedexamplebookexamples |
| ₁₁Na | 1s2 2s2 2p6 3s1 | |
| ₂₀Ca | 1s2 2s2 2p6 3s2 3p6 4s2 | |
| ₃₀Zn | 1s2 2s2 2p6 3s2 3p6 4s2 3d10 | 3d10 |
| • | Worked example 5.2 — new atoms | Workedexampleatoms |
| ₁₇Cl | 1s2 2s2 2p6 3s2 3p5 (2 + 2 + 6 + 2 + 5 = 17) | |
| ₂₆Fe | 1s2 2s2 2p6 3s2 3p6 4s2 3d6 (total 26) | total |
| ₃₅Br | 1s2 2s2 2p6 3s2 3p6 4s2 3d10 4p5 (total 35) | 3d10total |
| ₁₀Ne |
| ₁₈Ar |
| Worked example 5.3 — number of occupied levels and valence electrons. |
| PhosphorusThreemainshell |
| Notes on special cases. |
| stabilityhalffilledcompletely |
| Comparison aspect | Main idea | Keywords |
|---|---|---|
| • | Worked example 5.4 — unpaired electrons | Workedexampleunpairedelectrons |
| Carbon ₆C | 1s2 2s2 2px1 2py1: two unpaired electrons | 2px12py1unpairedelectrons |
| Oxygen |
| unpaired |
| Fluorine | one unpaired | unpaired |
| Neon | none | none |
| Phosphorus ₁₅P (3p3) | three unpaired electrons | threeunpairedelectrons |
| • |
| Workedexamplediagramcorrect |
| • | 2p must show one pair and two single electrons with parallel spins: [↑↓][↑][↑] | mustshowpairsingle |
| • |
| diagramshowingpairsempty |
| Worked example 5.6 — find the atomic number. | An atom has the configuration 1s2 2s2 2p6 3s2 3p6 4s1. The sum of the electrons is 19, so Z = 19 (potassium). In its ground state, its last electron has n = 4, ℓ = 0, mℓ = 0, ms = +½. | configurationelectronspotassiumground |
| Comparison aspect | Main idea | Keywords |
|---|---|---|
| Rutherford Alpha-Scattering Experiment |
| Landmarkprovingatommostly |
| Bohr Model of the Atom |
| Postulatedelectronsorbitnucleus |
| The Four Quantum Numbers | (1) Principal (n): energy level and size. (2) Azimuthal/Angular Momentum (l): orbital shape (s, p, d, f). (3) Magnetic (ml): orbital spatial orientation. (4) Spin (ms): electron intrinsic spin (+1/2 or -1/2). | Principalenergylevelsize |
| Aufbau Principle | Electrons occupy atomic orbitals of the lowest available energy levels before occupying higher levels: 1s < 2s < 2p < 3s < 3p < 4s < 3d | Electronsoccupyatomicorbitals |
| Hund’s Rule |
| Everyorbitalsubshellsingly |
| Comparison aspect | Main idea | Keywords |
|---|---|---|
| Photon Energy | ΔE = E₂ – E₁ = h ν = h c / λ | |
| • | Maximum electron capacity of principal energy level = 2n2 (valid only for n ≤ 4) | Maximumelectroncapacityprincipal |
| Subshell values |
| range |
| • | Number of orbitals per subshell = 2l + 1 | Magnetic quantum number ml from -l to +l | NumberorbitalssubshellMagnetic |
| De Broglie Wavelength | λ = h / (m v) (wave-particle duality) | particleduality |
| Comparison aspect | Main idea | Keywords |
|---|---|---|
| Why does the 4s subshell fill before the 3d subshell? |
| Becauseenergyloweraccording |
| Why is the 2n2 rule restricted to n ≤ 4? |
| Beyondlevelatomsbecome |
| Subshell | Azimuthal (l) | Number of Orbitals | Max Electrons | Spatial Geometry |
|---|---|---|---|---|
| s subshell | 0 | 1 orbital | 2 electrons | Spherical symmetrical |
| p subshell | 1 | 3 orbitals (px, py, pz) | 6 electrons | Dumbbell-shaped along x, y, z |
| d subshell | 2 | 5 orbitals | 10 electrons | Complex cloverleaf patterns |
| f subshell | 3 | 7 orbitals | 14 electrons | Multi-lobed complex geometry |
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