OAE Chemistry study materials
OAE Chemistry study resources

OAE Chemistry flashcards

OAE 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.

Hypothesis
A testable, falsifiable prediction about the relationship between variables, based on prior observations and used to guide experimental design.
Independent variable
The factor deliberately changed or manipulated by the experimenter to observe its effect on the dependent variable.
Accuracy vs precision
Accuracy is closeness to the true value; precision is reproducibility among repeated measurements. Random errors reduce precision; systematic errors reduce accuracy.
Significant figures
Digits in a measurement that carry meaning about precision. Nonzero digits and zeros between them count; leading zeros do not; trailing zeros after a decimal count.
Dimensional analysis
A problem-solving method using conversion factors so that unwanted units cancel, leaving the desired unit; e.g., 1 in = 2.54 cm.
Scientific theory
A well-substantiated explanation of some aspect of the natural world, supported by repeated evidence and subject to revision with new data.
Isotope
Atoms of the same element with the same number of protons but different numbers of neutrons, giving different mass numbers.
Average atomic mass
The weighted average of the masses of all naturally occurring isotopes of an element, calculated using their fractional abundances.
Bohr model
A model in which electrons occupy quantized energy levels around the nucleus; transitions between levels absorb or emit photons of specific energy.
Aufbau principle
Electrons fill atomic orbitals in order of increasing energy, starting with the lowest-energy orbital, to determine electron configurations.
Periodic trend: atomic radius
Atomic radius decreases across a period because effective nuclear charge increases, and increases down a group because additional electron shells are added.
Mole
The amount of substance containing 6.022×10^23 representative particles (Avogadro's number); its mass in grams equals the molar mass.
Ionic bond
An electrostatic attraction between oppositely charged ions formed by the transfer of electrons, typically between a metal and a nonmetal.
Covalent bond
A bond formed by the sharing of electron pairs between atoms, typically between nonmetals, creating molecules.
VSEPR theory
Valence Shell Electron Pair Repulsion theory predicts molecular shape by arranging electron domains around a central atom to minimize repulsion.
Hybridization
The mixing of atomic orbitals to form new hybrid orbitals that explain molecular geometry; sp, sp², and sp³ correspond to linear, trigonal planar, and tetrahedral arrangements.
Hydrogen bonding
A strong intermolecular force between a hydrogen atom bonded to N, O, or F and a lone pair on a nearby electronegative atom.
Limiting reactant
The reactant that is completely consumed first in a chemical reaction, determining the maximum amount of product that can form.
Percent yield
The ratio of actual yield to theoretical yield, multiplied by 100, expressing the efficiency of a reaction.
Mole ratio
The ratio of coefficients from a balanced chemical equation, used to convert moles of one substance to moles of another.
Net ionic equation
A chemical equation showing only the species that actually participate in the reaction, omitting spectator ions that remain unchanged.
Empirical formula
The simplest whole-number ratio of atoms of each element in a compound, determined from percent composition or experimental data.
Enthalpy change
The heat absorbed or released at constant pressure during a reaction; negative ΔH indicates exothermic, positive indicates endothermic.
Hess's law
The overall enthalpy change of a reaction equals the sum of enthalpy changes of its individual steps, allowing indirect determination of ΔH.
Gibbs free energy
A thermodynamic quantity defined as ΔG = ΔH – TΔS; a negative ΔG indicates a spontaneous process at constant temperature and pressure.
Activation energy
The minimum energy required for colliding particles to react; catalysts lower activation energy without being consumed.
Le Chatelier's principle
When a system at equilibrium is disturbed by a change in concentration, pressure, or temperature, it shifts to counteract the disturbance.
Molarity
A concentration unit defined as moles of solute per liter of solution, abbreviated M.
Colligative properties
Physical properties of solutions that depend on the number of solute particles, including boiling point elevation, freezing point depression, and osmotic pressure.
pH
A measure of acidity defined as –log[H3O+]; pH less than 7 is acidic, 7 is neutral, and greater than 7 is basic at 25°C.
Buffer
A solution containing a weak acid and its conjugate base (or weak base and conjugate acid) that resists large pH changes when acid or base is added.
Henderson–Hasselbalch equation
pH = pKa + log([A–]/[HA]), used to calculate the pH of a buffer solution from the ratio of conjugate base to weak acid.