KSEAB II PUC Chemistry study materials
KSEAB II PUC Chemistry study resources

KSEAB II PUC Chemistry flashcards

KSEAB II PUC Chemistry · Build recall with a focused review session.

32 cards. Read the term and the definition here. The deck at the top of this page is optional.

Avogadro constant
The number of particles present in one mole of a substance, equal to 6.022×10²³ mol⁻¹. It links the mass of a sample to the number of atoms or molecules it contains.
Limiting reagent
The reactant that is completely consumed first in a chemical reaction and therefore determines the maximum amount of product formed. Other reactants remain in excess.
Empirical formula
The formula showing the simplest whole-number ratio of atoms of each element in a compound. It is obtained from percentage composition by dividing by the smallest mole ratio.
Rydberg equation
1/λ = R_H Z²(1/n₁² − 1/n₂²) predicts the wavelength of light emitted when an electron falls between hydrogen atom energy levels. R_H equals 1.097×10⁷ m⁻¹.
Heisenberg uncertainty principle
It is impossible to determine both the position and momentum of an electron simultaneously with arbitrary precision. The product of the uncertainties is at least h/4π.
Hund's rule
Orbitals of equal energy are each occupied by one electron with parallel spins before any orbital receives a second electron, minimising electron repulsion.
Bond order
Half the difference between the number of bonding and antibonding electrons in a molecular orbital diagram. Higher bond order corresponds to a shorter and stronger bond.
VSEPR theory
Valence shell electron pair repulsion theory predicts molecular shape by arranging electron pairs around the central atom so that repulsions between them are minimised.
Hydrogen bond
An attractive force between a hydrogen atom covalently bonded to N, O or F and a lone pair on a nearby electronegative atom, raising boiling points of water and hydrogen fluoride.
Ideal gas equation
PV = nRT relates pressure, volume, amount and absolute temperature of an ideal gas. R equals 8.314 J K⁻¹ mol⁻¹ in SI units.
Hess's law
The enthalpy change of a reaction is independent of the route taken, so it can be calculated by summing the enthalpy changes of individual steps.
Gibbs energy criterion
ΔG = ΔH − TΔS determines spontaneity: a negative ΔG means the process is spontaneous, zero means equilibrium, and positive means non-spontaneous.
Le Chatelier's principle
When a system at equilibrium is disturbed by a change in concentration, pressure or temperature, the equilibrium shifts in the direction that counteracts the disturbance.
Buffer solution
A solution of a weak acid and its salt, or a weak base and its salt, that resists pH change on adding small amounts of acid or base.
Oxidising agent
A species that accepts electrons from another substance and is itself reduced. Its oxidation number decreases during the reaction.
Colligative properties
Properties of solutions that depend on the number of solute particles present rather than their nature: vapour pressure lowering, boiling point elevation, freezing point depression and osmotic pressure.
van't Hoff factor
The ratio of the observed colligative effect to the calculated value for a non-dissociating solute. It accounts for dissociation or association of solute particles.
Henry's law
The partial pressure of a gas above a solution is proportional to its mole fraction in the solution: p = K_H x. Solubility falls as temperature rises.
Nernst equation
E = E° − (0.0591/n) log Q at 25 °C gives the cell potential when concentrations are not standard, where Q is the reaction quotient.
First-order half-life
For a first-order reaction, t₁/₂ = 0.693/k. The half-life is constant and independent of the initial concentration of the reactant.
Arrhenius equation
k = A e^(−E_a/RT) shows that the rate constant increases with temperature and decreases with activation energy. A is the pre-exponential factor.
Lanthanoid contraction
The gradual decrease in atomic and ionic radii across the lanthanoid series caused by poor shielding of nuclear charge by 4f electrons.
Interstitial compounds
Compounds formed when small atoms such as hydrogen, carbon or nitrogen occupy the spaces between metal atoms in a crystal lattice, making the metal harder.
Crystal field splitting
The energy difference Δ_o between the d orbitals of a metal ion in a complex, produced by ligand repulsion. It determines colour and spin state.
Effective atomic number
EAN equals the atomic number of the metal minus its oxidation state plus twice the coordination number, estimating the electron count around the central ion.
SN1 mechanism
A two-step nucleophilic substitution in which the leaving group departs first to form a carbocation, followed by attack of the nucleophile. Tertiary halides react fastest.
Lucas test
A test using concentrated HCl and zinc chloride that distinguishes alcohols: tertiary gives immediate turbidity, secondary on warming, and primary does not react.
Tollens' reagent
An ammoniacal silver nitrate solution that is reduced by aldehydes to give a silver mirror, distinguishing aldehydes from ketones.
Hinsberg test
A reaction with benzenesulfonyl chloride that distinguishes amines: primary gives a soluble sulfonamide, secondary an insoluble one, and tertiary no reaction.
Peptide bond
An amide linkage formed between the carboxyl group of one amino acid and the amino group of another, with the elimination of a water molecule.
Vulcanisation
The process of heating natural rubber with sulphur to form cross-links between polymer chains, making the rubber harder, stronger and less sticky.
Flame test
A qualitative test in which a metal salt is heated in a flame and identified by its characteristic colour, such as golden yellow for sodium and lilac for potassium.