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 112th\frac{1}{12}\text{th} the mass of an atom of carbon-12.

  • Relative Atomic Mass (ArA_r)

    • Defined as the weighted mean mass of an atom of an element relative to 112th\frac{1}{12}\text{th} 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 1+1+ 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 (σ\sigma-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 (π\pi-bond)

    • A covalent bond formed by the sideways overlap of two parallel pp-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 (OH−OH^-) into the solution.

Energetics, Thermodynamics, and Reaction Kinetics

  • Specific Heat Capacity

    • Defined as the energy required to raise the temperature of 1 g1\,g of a substance by 1 K1\,K.

  • 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 (ΔrH∘\Delta_r H^\circ)

    • 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 (ΔfH∘\Delta_f H^\circ)

    • 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 (ΔcH∘\Delta_c H^\circ)

    • 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 (ΔneutH∘\Delta_{\text{neut}} H^\circ)

    • The enthalpy change that accompanies the neutralisation reaction of an acid by a base to form exactly one mole of H2OH_2O 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 −CH2−-CH_2- 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.