Chemistry: Electronic Structure, Periodic Trends, Bonding, and Molecular Formulas

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Comprehensive vocabulary flashcards covering atomic structure, electron configurations, PES, periodic trends, bonding, nomenclature, empirical/molecular formulas, Lewis structures, and octet exceptions.

Last updated 7:42 PM on 10/15/26
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37 Terms

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Aufbau Principle

A fill-up convention for adding electrons to orbitals in an atom stepwise across the periodic table, filling orbitals in order of increasing potential energy (PEPE).

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Pauli Exclusion Principle

The quantum mechanical principle stating that no two electrons in an atom can have the exact same set of four quantum numbers.

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Hund's Rule

The rule stating that electrons fill degenerate orbitals singly with parallel spins before pairing up with an opposite spin.

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Stern-Gerlach Experiment

An experiment demonstrating that electrons possess magnetic spin; when a beam of atoms with unpaired electrons passes through an external magnetic field, it splits into spin-up and spin-down states.

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Shell Model

An atomic model showing nuclear charge and energy levels (shells) with electrons arranged in concentric rings around the nucleus, without depicting subshells (s,p,d,fs, p, d, f).

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Effective Nuclear Charge (ZeffZ_{\text{eff}})

The net positive nuclear charge experienced by valence electrons, roughly approximated as the total nuclear charge (ZZ) minus core shielding electrons (SS).

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Photoelectron Spectroscopy (PES)

An analytical technique that measures the relative number of electrons and their average binding/potential energies (ΔUE\Delta U_E) to visualize orbital electron arrangements.

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<p>Scandium Photoelectron Spectrum</p>

Scandium Photoelectron Spectrum

The experimental PES spectrum showing binding energy peaks for scandium: 433 MJ/mol433\,\text{MJ/mol} (1s21s^2), 48.5 MJ/mol48.5\,\text{MJ/mol} (2s22s^2), 39.2 MJ/mol39.2\,\text{MJ/mol} (2p62p^6), 5.44 MJ/mol5.44\,\text{MJ/mol} (3s23s^2), 3.24 MJ/mol3.24\,\text{MJ/mol} (3p63p^6), 0.77 MJ/mol0.77\,\text{MJ/mol} (3d13d^1), and 0.63 MJ/mol0.63\,\text{MJ/mol} (4s24s^2).

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Electronegativity (EN)

An atom's tendency to attract and hang onto its valence electrons or pull on a shared bonded pair within a compound.

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Metallic Character (MC)

The tendency of an atom to hold onto its valence electrons less fiercely, which increases as electronegativity decreases.

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Electron Affinity (EA)

The energy change associated with adding an electron to a neutral gaseous atom to form an anion (Atom+1e−→Anion\text{Atom} + 1e^- \rightarrow \text{Anion}).

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Atomic Radius Trend

A periodic trend where atomic size decreases across a period due to increasing nuclear attraction at similar distances, and increases down a group due to the addition of electron shells.

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Cationic Radius

The radius of a positive ion, which is smaller than its neutral atom because the loss of valence electrons increases ZeffZ_{\text{eff}} and the inward attractive force on remaining electrons.

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Anionic Radius

The radius of a negative ion, which is larger than its neutral atom because adding electrons increases inter-electron repulsion while ZeffZ_{\text{eff}} remains unchanged.

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Ionic Bonding

A type of chemical bonding typically occurring between metals and nonmetals with a large ΔEN\Delta\text{EN}, forming a crystal lattice where valence electrons are localized on anions.

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Covalent Bonding

A type of chemical bonding typically between nonmetals with a small ΔEN\Delta\text{EN} and high electronegativity, where valence electrons are shared and localized between bonded atoms.

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Metallic Bonding

A type of chemical bonding among metal atoms with low electronegativity, characterized by valence electrons delocalized freely across all atoms in the solid.

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Classical Cation Suffixes (-ic / -ous)

Nomenclature rules where the suffix '-ic' indicates the cation with the higher charge state (e.g., cupric, Cu2+\text{Cu}^{2+}) and '-ous' indicates the cation with the lower charge state (e.g., cuprous, Cu+\text{Cu}^+).

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Oxyanion Suffixes (-ate / -ite)

Nomenclature rules where '-ate' designates the oxyanion containing more oxygen atoms (e.g., SO42−\text{SO}_4^{2-}, sulfate) and '-ite' designates the oxyanion containing fewer oxygen atoms (e.g., SO32−\text{SO}_3^{2-}, sulfite).

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Oxyanion Prefixes (per- / hypo-)

Nomenclature modifiers used in extended oxyanion series, where 'per-' indicates the most oxygen atoms (e.g., ClO4−\text{ClO}_4^-, perchlorate) and 'hypo-' indicates the fewest oxygen atoms (e.g., ClO−\text{ClO}^-, hypochlorite).

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Hydrated Salt

An ionic compound containing a specific molar ratio of water molecules trapped within its crystal lattice (e.g., NiCl2⋅6H2O\text{NiCl}_2 \cdot 6\text{H}_2\text{O}, nickel(II) chloride hexahydrate).

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Protic Acid

A molecule capable of acting as a source of a hydrogen ion (H+\text{H}^+) in an aqueous solution.

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Binary Acid

An acid consisting of hydrogen bonded to a single other element, whose strength increases as the H−X\text{H}-\text{X} bond length increases and weakens (e.g., HF<HCl<HBr<HI\text{HF} < \text{HCl} < \text{HBr} < \text{HI}).

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Oxyacid

An acid containing hydrogen bonded to an oxyanion, whose acidic strength increases with the number of attached oxygen atoms or higher electronegativity of neighboring atoms.

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Formula Mass

The total mass in g/mol\text{g/mol} of a compound, calculated by summing the molar masses of each constituent atom in its chemical formula.

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Percent Composition

The percentage of a sample's total mass contributed by a specific component element, calculated as mass partmass whole×100\frac{\text{mass part}}{\text{mass whole}} \times 100.

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Empirical Formula (EF)

The simplest chemical formula representing the lowest whole-number mole ratio of elements in a compound.

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Molecular Formula (MF)

The formula that indicates the actual number of atoms of each element in a molecule, related to the empirical formula by MF=n×EF\text{MF} = n \times \text{EF}.

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Lewis Structure

A 2D structural diagram illustrating bonding within molecules or polyatomic ions using lines for shared electron pairs and dots for non-bonded electrons.

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Formal Charge (FC)

A bookkeeping value estimating an atom's electric charge in a Lewis structure, calculated as FC=valence e−−12(bonded e−)−(non-bonded e−)\text{FC} = \text{valence } e^- - \frac{1}{2}(\text{bonded } e^-) - (\text{non-bonded } e^-).

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Bond Polarity

The asymmetric distribution of electron density in a covalent bond caused by differences in electronegativity, producing partial positive (δ+\delta^+) and partial negative (δ−\delta^-) charges.

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Hypovalent

A state in which a central atom in a Lewis structure possesses fewer than eight valence electrons prior to forming multiple bonds.

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Incomplete Octet

A stable Lewis structure configuration in which the central atom remains surrounded by fewer than eight valence electrons (e.g., boron in BF3\text{BF}_3).

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Free Radical

A reactive chemical species containing an odd total number of valence electrons that features at least one single unpaired electron (e.g., NO2\text{NO}_2 or ClO\text{ClO}).

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Resonance Structures

Two or more valid Lewis structures for a single chemical species that differ only in the distribution and arrangement of delocalized electrons.

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Resonance Hybrid

The true, weighted-average structure representing a resonance-stabilized species, featuring fractional bonds and delocalized charge across equivalent atoms.

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Extended Octet

An expanded valence shell where a central element in Period 3 or beyond is surrounded by more than eight electrons using accessible, empty dd-orbitals.