Definitions Flashcards
Isotope
Atoms of the same element with a different number of neutrons but the same number of protons
Relative isotopic mass
Mass of an isotope relative to the 1/12th of the mass of a carbon-12 atom
Relative atomic mass
Weighted mean mass of an atom relative to the 1/12th of the mass of a carbon-12
Empirical formula
Simplest whole number ratio of atoms of each elements present in a compound
Molecular formula
Actual number and type of atoms of each element in a molecule
Anhydrous
Without waters of crystallisation
Hydrous
With water of crystallisation
Water of crystallisation
Water crystals that are trapped in a compound’s lattice structure
Orbital
3D regions of space around the nucleus that can hold up to 2 electrons with opposite spins
Covalent bond
Strong electrostatic attraction between a shared pair of electrons and the nuclei of the bonded atoms
Dative covalent bond
Covalent bond where one atoms donates both the electrons in a bonded pair
Ionic bonding
Electrostatic attraction between positive and negative ions
Ion
Charged particles formed from the loss of gain of electrons
Electronegativity
Ability of an atom the attract the bonding electrons in a covalent bond
Redox reaction
Reaction where both reduction and oxidation take place
Metallic bonding
Strong electrostatic attraction between cations and delocalised electrons
First ionisation energy
Energy required to remove one moles of electrons from one mole of gaseous atoms to form 1 moles of gaseous 1+ ions
Periodicity
Repeating patterns seen across the periods of the periodic table
Activation energy
Minimum energy required for a reaction to take place
Standard conditions
100kPa and 298K
Homologous series
Series of organic compounds have the same functional group with each successive member differing by CH2
Structural isomers
Compounds with the same molecular formula but a different structural formulae
Homolytic fission
Each bonding atom receives one electron from the bonded pair, forming two radicals
Heterolytic fission
One bonding atom receives both electrons from the bonded pair
Radical
Any species with an unpaired electron
Stereoisomers
Compounds with the same structural formula but with a different arrangement in space
E/Z isomerism
Example of stereoisomerism caused by restricted rotation about a double bond, requiring two different groups to be attached to each carbon atom of the alkene group.
Nucleophile
Electron pair donor
Electrophile
Electron pair acceptor