Comprehensive Guide to Core Chemistry Definitions and Principles
Fundamental Atomic Structure and Quantitative Mass Definitions
Isotope
Defined as atoms of the same element with the same number of protons (identical atomic number) but a different number of neutrons.
Chemical properties: Isotopes have identical chemical properties because they have the same electron configuration.
Physical properties: Isotopes exhibit slightly different physical properties due to differences in mass.
Relative Isotopic Mass
Defined as the mass of an isotope relative to the mass of an atom of carbon-12.
Relative Atomic Mass ()
Defined as the weighted mean mass of an atom of an element relative to the mass of an atom of carbon-12.
Empirical Formula
Defined as the simplest whole number ratio of atoms of each element present in a compound.
Atom Economy
A quantitative measure of a chemical reaction indicating how well reactant atoms have been utilised in forming the desired products.
First Ionisation Energy
Defined as the energy required to remove one electron from each atom in one mole of gaseous atoms of an element to form one mole of gaseous ions.
Chemical Bonding and Orbital Interactions
Ionic Bonding
The electrostatic attraction between oppositely charged ions: positive ions (cations) and negative ions (anions), typically formed between metals and non-metals.
Covalent Bonding
The strong electrostatic attraction between a shared pair of electrons and the positive nuclei of the bonded atoms.
Dative Covalent Bond (Coordinate Bond)
A specific type of covalent bond in which the shared pair of electrons has been supplied solely by one of the bonding atoms.
Metallic Bonding
The strong electrostatic attraction between fixed metal cations and a surrounding "sea" of delocalised electrons.
Sigma Bond (-bond)
A covalent bond resulting from the direct, head-on overlap of two atomic orbitals, with one orbital contributed from each bonding atom.
Pi Bond (-bond)
A covalent bond formed by the sideways overlap of two parallel -orbitals, with one contributed from each carbon atom involved in a double bond.
Acids, Bases, and Aqueous Solutions
Strong Acid
An acid that dissociates completely into its ions when dissolved in an aqueous solution.
Weak Acid
An acid that only partially dissociates into its ions in an aqueous solution, establishing an equilibrium between the undissociated acid and its ions.
Alkali
A specific type of base that dissolves in water to release hydroxide ions () into the solution.
Energetics, Thermodynamics, and Reaction Kinetics
Specific Heat Capacity
Defined as the energy required to raise the temperature of of a substance by .
Average Bond Enthalpy
Defined as the energy required to break one mole of a specified covalent bond in a gaseous molecule.
This value is calculated as an average across a wide range of different chemical compounds containing that specific bond type.
Standard Enthalpy Change of Reaction ()
The enthalpy change that accompanies a chemical reaction occurring in the exact molar quantities shown in the balanced chemical equation under standard conditions, with all reactants and products in their standard states.
Standard Enthalpy Change of Formation ()
The enthalpy change that takes place when one mole of a compound is formed directly from its constituent elements under standard conditions, with all reactants and products in their standard states.
Standard Enthalpy Change of Combustion ()
The enthalpy change that takes place when one mole of a substance reacts completely with oxygen under standard conditions, with all reactants and products in their standard states.
Standard Enthalpy Change of Neutralisation ()
The enthalpy change that accompanies the neutralisation reaction of an acid by a base to form exactly one mole of under standard conditions, with all reactants and products in their standard states.
Catalyst
A substance that alters the rate of a chemical reaction without undergoing any permanent chemical change itself.
Organic Chemistry: Classifications, Structure, and Isomerism
Homologous Series
A series or family of organic compounds sharing identical functional groups and similar chemical properties, where each successive member differs from the preceding one by a unit.
Functional Group
The specific atom or group of atoms within an organic molecule that is largely responsible for its characteristic chemical properties and reactions.
Carbon Skeleton Classifications
Aliphatic: Organic compounds containing carbon atoms joined to each other in straight chains, branched chains, or non-aromatic rings.
Alicyclic: Aliphatic compounds where carbon atoms are joined specifically in a non-aromatic ring structure.
Aromatic: Organic compounds containing a benzene ring (or aromatic ring system).
Isomerism
Structural Isomers: Compounds sharing the exact same molecular formula but possessing different structural formulae.
Stereoisomers (Sterioisomers): Compounds that have the same structural formula but possess different spatial arrangements of their atoms in three dimensions.
Organic Reaction Mechanisms and Reactive Species
Bond Fission Mechanisms
Homolytic Fission: The breaking of a covalent bond in which the shared electron pair is divided equally between the two bonded atoms, with each atom taking one electron to form two radicals.
Heterolytic Fission: The breaking of a covalent bond in which the shared electron pair is retained entirely by one of the bonded atoms, resulting in the formation of charged ions.
Reactive Species
Radical: A neutral chemical species possessing an unpaired electron, typically formed via homolytic fission.
Electrophile: An electron-deficient species that is attracted to an electron-rich centre and acts as an electron pair acceptor.
Nucleophile (Neucleophile): An electron-rich species that acts as an electron pair donor.