LC Chemistry study materials
LC Chemistry study resources

LC Chemistry flashcards

LC Chemistry · Build recall with a focused review session.

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

Atomic number
The number of protons in the nucleus of an atom; it defines the element and equals the number of electrons in a neutral atom.
Isotopes
Atoms of the same element with the same proton number but different neutron numbers, so they have different mass numbers and slightly different physical properties.
First ionisation energy
The energy needed to remove one mole of electrons from one mole of gaseous atoms to form one mole of gaseous 1+ ions.
Aufbau principle
Electrons occupy the lowest available energy orbital first, filling in the order 1s, 2s, 2p, 3s, 3p, 4s, 3d and so on.
Ionic bond
The electrostatic attraction between oppositely charged ions formed by complete transfer of electrons from a metal atom to a non-metal atom.
Hydrogen bonding
A strong intermolecular attraction between a hydrogen atom bonded to N, O or F and a lone pair on a nearby electronegative atom.
VSEPR theory
Electron pairs around a central atom repel each other and arrange as far apart as possible, determining the molecular shape and bond angles.
Sigma bond
A covalent bond formed by end-on overlap of orbitals, with electron density concentrated along the line joining the two nuclei; rotation is possible.
Limiting reagent
The reactant that is completely consumed first in a reaction; it determines the maximum amount of product that can be formed.
Percentage yield
The actual mass of product obtained expressed as a percentage of the theoretical maximum mass calculated from the balanced equation and limiting reagent.
Molar volume of gas
The volume occupied by one mole of any gas under specified conditions: about 24 dm³ at room temperature and pressure, 22.7 dm³ at STP.
Empirical formula
The simplest whole-number ratio of atoms of each element in a compound, obtained by dividing mole ratios by the smallest value.
Spectator ions
Ions present in a reaction mixture that are unchanged on both sides of the equation and are therefore omitted from the net ionic equation.
Oxidation number
A number assigned to an element in a compound representing the charge it would carry if all bonds were treated as ionic; oxidation is an increase.
Precipitation reaction
A reaction in which two soluble salts in solution exchange ions to form an insoluble solid product that separates from the mixture.
Equivalence point
The point in a titration where the amount of titrant added exactly reacts with the amount of substance in the flask, according to the stoichiometry.
Buffer solution
A solution of a weak acid and its conjugate base that resists significant pH change when small amounts of acid or alkali are added.
pH definition
The negative logarithm to base ten of the hydrogen ion concentration in mol dm⁻³; a change of one pH unit means a tenfold concentration change.
Ideal gas law
The relationship pV = nRT linking pressure, volume, amount of gas and absolute temperature; R is the universal gas constant 8.314 J K⁻¹ mol⁻¹.
Dalton's law
The total pressure exerted by a mixture of non-reacting gases equals the sum of the partial pressures that each gas would exert alone.
Absolute temperature
Temperature measured on the kelvin scale, obtained by adding 273 to the Celsius value; it must be used in all gas law calculations.
Colligative properties
Properties such as boiling point elevation, freezing point depression and osmotic pressure that depend on the number of dissolved particles, not their identity.
Molality
The amount of solute in moles dissolved in one kilogram of solvent; unlike molarity it does not change with temperature.
Osmotic pressure
The pressure needed to prevent net movement of solvent across a semipermeable membrane into a solution; given by π = iMRT.
Hess's law
The total enthalpy change of a reaction is the same regardless of the route taken, allowing enthalpy changes to be calculated by summing steps.
Activation energy
The minimum kinetic energy that colliding particles must possess for a reaction to occur; a catalyst lowers it without changing the enthalpy change.
Dynamic equilibrium
A state in a reversible reaction where the forward and reverse rates are equal, so concentrations stay constant while both reactions continue.
Le Chatelier's principle
When a system at equilibrium is disturbed by a change in concentration, pressure or temperature, it shifts to oppose the change.
Equilibrium constant Kc
The ratio of product concentrations to reactant concentrations, each raised to its stoichiometric power, at equilibrium; it depends only on temperature.
Electrophilic addition
A reaction of an alkene in which an electron-rich double bond attacks an electrophile, forming a carbocation intermediate that is then attacked by a nucleophile.
Esterification
The reversible reaction of a carboxylic acid with an alcohol, catalysed by concentrated sulfuric acid, producing an ester and water.
Electrolysis
The decomposition of a compound by passing a direct electric current through it in molten or aqueous form, with oxidation at the anode and reduction at the cathode.
Standard electrode potential
The potential of a half-cell measured against the standard hydrogen electrode under standard conditions of 298 K, 1 mol dm⁻³ and 100 kPa.
Faraday constant
The electric charge carried by one mole of electrons, approximately 96 500 coulombs per mole; used to relate charge passed to moles of substance electrolysed.
Concordant titres
Repeat titration volumes that agree closely, usually within 0.10 cm³ of each other, allowing a reliable mean to be calculated.
Weighing by difference
A technique where the mass of substance transferred is found by subtracting the final container mass from the initial mass, reducing transfer error.