ILTS Science: Chemistry (240) study materials
ILTS Science: Chemistry (240) study resources

ILTS Science: Chemistry (240) cheat sheet

ILTS Science: Chemistry (240) · Keep the key ideas within reach.

Quick reference

Foundations of Scientific Inquiry and the Nature of Science

  • Scientific inquiry cycle: question → hypothesis → controlled experiment → data analysis → conclusion → peer review and replication; a single unreplicated study is provisional evidence.

  • Independent variable is manipulated by the investigator; dependent variable is measured; controlled variables are held constant to isolate cause and effect.

  • A hypothesis must be falsifiable: it predicts a specific, testable outcome that could disconfirm it. Unfalsifiable claims fall outside empirical science.

  • Accuracy = closeness to the accepted/true value; precision = reproducibility among repeated measurements. Random error affects precision; systematic error shifts accuracy.

  • Percent error = |accepted − experimental| / accepted × 100%. Percent difference compares two experimental values without an accepted standard.

  • Significant figures: nonzero digits and interior zeros count; leading zeros do not; trailing zeros count only with a decimal point. Addition/subtraction keeps the least decimal places; multiplication/division keeps the least significant figures.

  • Scientific law describes a consistent observed relationship (e.g., conservation of mass); a theory explains why, and is supported by broad, repeated evidence. Theories do not become laws.

  • Peer review, replication, and independent verification distinguish science from pseudoscience; consensus can shift when new reproducible evidence appears.

  • Graph choice: line graph for continuous independent variables, bar chart for categorical comparisons, scatter plot with regression for correlation between two measured variables.

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Chemistry Content: Matter, Atomic Structure, and Periodicity

  • Classification: pure substances (elements, compounds) have fixed composition; mixtures (homogeneous, heterogeneous) do not. Physical changes alter state or form; chemical changes form new substances.

  • Atomic number Z = protons; mass number A = protons + neutrons; isotopes share Z but differ in neutrons; ions differ in electrons.

  • Average atomic mass = Σ(fractional abundance × isotopic mass). Charge of an ion = protons − electrons.

  • Bohr model: E = −13.6 eV/n² for hydrogen; photon energy absorbed or emitted = hf = ΔE between levels; h = 6.626 × 10⁻³⁴ J·s.

  • Quantum numbers: n (shell, n ≥ 1), ℓ (0 to n−1, shape), mℓ (−ℓ to +ℓ, orientation), ms (±½, spin). Pauli exclusion forbids identical sets of all four.

  • Electron configuration follows Aufbau order, Hund's rule (maximize unpaired spins in degenerate orbitals), and the octet/duet stability principle; Cr and Cu are exceptions.

  • Periodic trends: atomic radius decreases left→right and increases top→bottom; ionization energy and electronegativity increase left→right and decrease top→bottom.

  • Effective nuclear charge increases across a period, contracting the shell and raising ionization energy; added shells down a group shield and expand radius.

  • Mole concept: 1 mol = 6.022 × 10²³ particles; molar mass in g/mol; n = m/M; molar volume of ideal gas at STP (0 °C, 1 atm) = 22.4 L/mol.

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Chemistry Content: Chemical Bonding, Reactions, and Stoichiometry

  • Bond type by electronegativity difference: <0.4 nonpolar covalent, 0.4–1.7 polar covalent, >1.7 largely ionic; metallic bonding involves delocalized electrons.

  • VSEPR: electron domains repel to maximize separation; lone pairs occupy more space than bonding pairs, compressing bond angles (CH₄ 109.5°, NH₃ 107°, H₂O 104.5°).

  • Molecular polarity requires polar bonds plus an asymmetric geometry; CO₂ is nonpolar despite polar bonds, H₂O is polar.

  • Intermolecular forces ranked: ion–dipole > hydrogen bonding > dipole–dipole > London dispersion; stronger forces raise boiling point and surface tension.

  • Reaction types: synthesis, decomposition, single replacement, double replacement (precipitation), combustion, and acid–base neutralization.

  • Balance equations by conservation of atoms and charge; coefficients give mole ratios used in stoichiometric conversions.

  • Limiting reactant: compute moles of product from each reactant; the smallest yield identifies the limiting reagent; excess reagent remains unreacted.

  • Percent yield = actual/theoretical × 100%; molarity M = mol solute/L solution; dilution M₁V₁ = M₂V₂.

  • Net ionic equations omit spectator ions; solubility rules predict precipitate formation (e.g., most nitrates and alkali-metal salts are soluble).

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Chemistry Content: Thermochemistry, Kinetics, and Equilibrium

  • First law: ΔE = q + w; enthalpy change at constant pressure q = ΔH. Exothermic ΔH < 0; endothermic ΔH > 0.

  • Calorimetry: q = mcΔT; Hess's law sums stepwise ΔH; ΔH°rxn = ΣΔH°f(products) − ΣΔH°f(reactants).

  • Bond breaking absorbs energy; bond formation releases energy. Entropy ΔS increases with gas production, temperature, and disorder.

  • Gibbs free energy: ΔG = ΔH − TΔS; spontaneous at constant T and P when ΔG < 0; ΔG° = −RT ln K.

  • Rate law: rate = k[A]^m[B]^n; orders determined experimentally, not from coefficients. Rate constant k depends on temperature via Arrhenius k = Ae^(−Ea/RT).

  • Collision theory: reaction requires sufficient energy (Ea) and correct orientation; catalysts lower Ea without changing ΔH or equilibrium position.

  • Equilibrium: forward and reverse rates equal; K = products^coefficients / reactants^coefficients (pure solids/liquids omitted). Q < K shifts right; Q > K shifts left.

  • Le Chatelier: adding reactant shifts right; increasing pressure shifts toward fewer gas moles; heating favors the endothermic direction.

  • Half-life first order: t½ = 0.693/k; concentration decays as [A] = [A]₀e^(−kt).

Quick reference

Chemistry Content: Solutions, Acids and Bases, and Electrochemistry

  • Solution concentration: molarity M = mol/L; molality m = mol solute/kg solvent; mole fraction and mass percent are temperature-independent alternatives.

  • Colligative properties depend on particle count: ΔTb = iKb·m and ΔTf = iKf·m; van't Hoff factor i accounts for dissociation (NaCl → i ≈ 2).

  • Solubility of most solids rises with temperature; gas solubility falls with temperature and rises with partial pressure (Henry's law).

  • Brønsted–Lowry: acid donates a proton, base accepts one; conjugate pairs differ by one H⁺. Lewis acid accepts an electron pair.

  • pH = −log[H₃O⁺]; pOH = −log[OH⁻]; pH + pOH = 14 at 25 °C; Kw = 1.0 × 10⁻¹⁴.

  • Strong acids/bases ionize completely; weak acids use Ka: Ka·Kb = Kw for a conjugate pair; pKa = −log Ka.

  • Buffer: weak acid plus conjugate base resists pH change; Henderson–Hasselbalch pH = pKa + log([A⁻]/[HA]).

  • Titration equivalence: moles acid = moles base adjusted by stoichiometric coefficients; strong–strong equivalence pH = 7 at 25 °C.

  • Electrochemistry: oxidation at anode, reduction at cathode (An Ox, Red Cat); E°cell = E°cathode − E°anode; ΔG° = −nFE°cell; positive E°cell means spontaneous galvanic cell.

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Chemistry Content: Organic Chemistry, Biochemistry, and Nuclear Chemistry

  • Hydrocarbon families: alkanes (single bonds, CnH2n+2), alkenes (one double, CnH2n), alkynes (one triple, CnH2n−2); IUPAC naming uses the longest chain and lowest locants.

  • Functional groups: hydroxyl (alcohol), carbonyl (aldehyde/ketone), carboxyl (acid), amino, ester, amide, ether, and phosphate; each dictates characteristic reactivity.

  • Isomers share molecular formula but differ in connectivity (structural) or spatial arrangement (cis–trans, enantiomers).

  • Common reaction patterns: substitution (alkanes, aromatics), addition (alkenes/alkynes), elimination, oxidation of alcohols, esterification, and polymerization.

  • Biomolecules: carbohydrates (monosaccharides → polysaccharides), proteins (amino acids linked by peptide bonds), lipids (fatty acids, triglycerides), nucleic acids (nucleotides with sugar, phosphate, base).

  • Enzymes are biological catalysts that lower activation energy and are specific to substrates; denaturation disrupts tertiary structure and activity.

  • Nuclear notation: mass number A = protons + neutrons; alpha decay reduces A by 4 and Z by 2; beta-minus decay raises Z by 1; gamma emission changes neither.

  • Nuclear stability: neutron-to-proton ratio; band of stability; half-life and radioactive decay follow first-order kinetics.

  • Fission splits a heavy nucleus releasing energy; fusion combines light nuclei; both convert mass to energy via E = mc².

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Science Laboratory Safety, Techniques, and Data Analysis

  • Safety priority order: protect people, then contain the hazard, then clean up; know eyewash, shower, fire extinguisher, and spill kit locations before starting.

  • Goggles and appropriate PPE are required whenever chemicals, heat, or glassware under pressure are used; never taste or directly smell chemicals.

  • Acid spill on skin: flush with copious water for at least 15 minutes; add acid to water (never water to acid) when diluting.

  • Heating: use a water bath or heating mantle for flammable solvents; never heat a closed system; point test-tube mouths away from people.

  • Glassware: volumetric flasks and pipettes are for measuring; graduated cylinders for approximate volumes; never use graduated cylinders for accurate volumetric work.

  • Separation techniques: filtration (insoluble solid), distillation (boiling-point difference), chromatography (differential affinity), extraction (solubility difference).

  • Data analysis: identify outliers, calculate mean and standard deviation, plot calibration curves, and report units with correct significant figures.

  • Experimental design: include a control group, replicate trials, randomize or standardize conditions, and record raw data before processing.

  • Waste disposal follows local and institutional rules; never pour chemicals down the drain unless explicitly authorized.

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Pedagogical Content Knowledge and Instructional Practice in Chemistry

  • 5E model (Engage, Explore, Explain, Elaborate, Evaluate) sequences inquiry: exploration precedes formal explanation to build concepts from evidence.

  • Three levels of chemistry representation: macroscopic (observable), symbolic (formulas, equations), and particulate (atoms, molecules); instruction should connect all three.

  • Common misconceptions to target: conservation of mass in open systems, mole as a mass rather than a count, equilibrium as a static state, and bonds releasing energy when broken.

  • Assessment alignment: formative checks (exit tickets, concept inventories) guide instruction; summative assessments match stated learning objectives and cognitive demand.

  • Laboratory pedagogy: pre-lab planning, explicit safety instruction, and post-lab analysis develop inquiry and data-literacy skills; modeling and simulations supplement hands-on work.

  • Differentiation: tiered tasks, multiple representations, and scaffolds (graphic organizers, worked examples) support diverse learners, including English learners.

  • Argumentation from evidence: students should construct claims supported by data and reasoning, and critique peer explanations using scientific criteria.

  • Disciplinary literacy: teach reading of procedures, data tables, and chemical notation explicitly; use precise vocabulary and sentence frames for explanation.