Periodic Trends, Halogens, and Transition Elements

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Comprehensive practice flashcards covering periodic properties, halogen group trends and reactions, and the general features, configurations, oxidation states, complexes, and catalytic properties of transition metals.

Last updated 4:06 PM on 10/14/26
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50 Terms

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Nuclear Charge

The total positive electric charge of an atomic nucleus, which is equal to the number of protons (ZZ) present in the nucleus.

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

The net positive charge that actually acts on a valence shell electron, determined by the formula Zeff=Z−SZ_{\text{eff}} = Z - S, where ZZ is the atomic number and SS is the number of shielding or core electrons.

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Shielding Effect

The reduction in nuclear electrostatic attraction experienced by outer valence electrons due to repulsive forces from inner-shell core electrons.

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Atomic Radius

The measured distance from the atomic nucleus to the outermost electron shell; it decreases across a period due to increasing effective nuclear charge and increases down a group due to the addition of occupied shells.

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Cation Radius

The ionic radius of a positively charged ion, which is consistently smaller than the parent neutral atom because the loss of electrons decreases electron-electron repulsions.

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Anion Radius

The ionic radius of a negatively charged ion, which is consistently larger than the parent neutral atom because the addition of electrons increases mutual electron repulsions, causing the electron cloud to spread out.

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Ionization Energy

The quantity of energy required to remove an electron from the ground state of an isolated gaseous atom or ion; it increases across a period and decreases down a group.

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Successive Ionization Energy

The progressively greater energy required to remove second, third, or subsequent electrons from an ion as the radius contracts and the remaining electrons are pulled closer to the nucleus.

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Aluminum Fourth Ionization Energy Jump

The dramatic increase between aluminum's third ionization energy (2745 kJ2745\,\text{kJ}) and fourth ionization energy (11577 kJ11577\,\text{kJ}), caused by attempting to remove an electron from a stable noble-gas octet core (Al3+\text{Al}^{3+}).

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Electron Affinity

The energy change that occurs when an electron is added to a gaseous atom to form an anion; values generally become more negative across a period and less negative down a group.

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Fluorine-Chlorine Electron Affinity Anomaly

The exception where chlorine has a greater electron affinity (−349 kJ mol−1-349\,\text{kJ}\,\text{mol}^{-1}) than fluorine (−328 kJ mol−1-328\,\text{kJ}\,\text{mol}^{-1}) due to fluorine's exceptionally small atomic volume, which produces intense electron-electron repulsion against incoming electrons.

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Electronegativity

A relative measure of the tendency of an atom within a covalent molecule to attract shared pairs of bonding electrons toward itself.

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Halogens

The highly reactive non-metallic elements found in Group VIIA (Group 17) of the periodic table, possessing seven valence electrons (ns2np5ns^2 np^5); the name translates to 'salt-former'.

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Diatomic Halogen Molecules

Non-polar homonuclear molecules (F2\text{F}_2, Cl2\text{Cl}_2, Br2\text{Br}_2, and I2\text{I}_2) formed by two identical halogen atoms sharing a pair of electrons via a single covalent bond to complete their octets.

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Sublimation

The physical process in which a solid transitions directly into a gas without melting into a liquid, as observed when solid iodine crystals are heated gently to yield a purple vapour.

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Van der Waals Forces in Halogens

Weak intermolecular attractions that become stronger down Group 17 as molecular size increases, causing melting and boiling points to rise from fluorine to iodine.

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Fluorine Physical Appearance

A pale yellow gas at room temperature that exhibits an extremely low density of 0.0017 g cm−30.0017\,\text{g}\,\text{cm}^{-3}, a melting point of −220∘C-220^\circ\text{C}, and a boiling point of −118∘C-118^\circ\text{C}.

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Chlorine Physical Appearance

A pale green gas at room temperature with a density of 0.0032 g cm−30.0032\,\text{g}\,\text{cm}^{-3}, a melting point of −101∘C-101^\circ\text{C}, and a boiling point of −34∘C-34^\circ\text{C}.

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Bromine Physical Appearance

A dense, dark red volatile liquid with a density of 3.10 g cm−33.10\,\text{g}\,\text{cm}^{-3}, a melting point of −7∘C-7^\circ\text{C}, and a boiling point of 59∘C59^\circ\text{C} that produces dark orange-red fumes.

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Iodine Physical Appearance

A shiny, grey-black solid with a density of 4.93 g cm−34.93\,\text{g}\,\text{cm}^{-3}, a melting point of 114∘C114^\circ\text{C}, and a boiling point of 184∘C184^\circ\text{C} that readily produces a purple vapour upon heating.

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Fluorine Oxidation State Restriction

The strict chemical limitation whereby fluorine exhibits only a −1-1 oxidation state, because it is the most electronegative element and completely lacks valence d-orbitals to expand its octet.

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Halogen Octet Expansion

The ability of chlorine, bromine, and iodine to use low-lying vacant d-orbitals to achieve positive oxidation states of +1+1, +3+3, +5+5, and +7+7 when combined with small, highly electronegative atoms like fluorine and oxygen.

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Disproportionation of Chlorine

A redox reaction in which elemental chlorine is simultaneously oxidized and reduced upon dissolving in water: Cl2+H2O→HCl+HOCl\text{Cl}_2 + \text{H}_2\text{O} \rightarrow \text{HCl} + \text{HOCl}.

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Chlorine Water

An aqueous equilibrium solution containing dissolved Cl2(aq)\text{Cl}_2(aq), hydrochloric acid (HCl(aq)\text{HCl}(aq)), and chloric(I) acid (HOCl(aq)\text{HOCl}(aq)).

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Hypochlorite Ion (OCl−\text{OCl}^-)

A potent oxidizing ion in chlorine water that acts as a bleaching agent by decolourizing dyes (OCl−+dyecoloured→Cl−+dyecolourless\text{OCl}^- + \text{dye}_{\text{coloured}} \rightarrow \text{Cl}^- + \text{dye}_{\text{colourless}}) and decomposes under heat or light: 2OCl−→O2+2Cl−2\text{OCl}^- \rightarrow \text{O}_2 + 2\text{Cl}^-.

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Halogen Displacement Reaction

A redox process in which a more reactive, higher-electronegativity halogen oxidizes and displaces a less reactive halide ion from its aqueous salt solution.

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Reducing Ability of Halide Ions

The trend in which the tendency of halide ions to lose electrons increases down the group (I−>Br−>Cl−>F−\text{I}^- > \text{Br}^- > \text{Cl}^- > \text{F}^-) due to increasing ionic size and shielding.

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Oxidizing Ability of Halogens

The trend in which the power of elemental halogens to act as electron acceptors decreases down the group (F2>Cl2>Br2>I2\text{F}_2 > \text{Cl}_2 > \text{Br}_2 > \text{I}_2) due to declining effective nuclear pull on valence levels.

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Silver Halides in Photography

Photosensitive compounds coated on film emulsions that decompose upon exposure to light via the reaction Ag++e−→Ag\text{Ag}^+ + e^- \rightarrow \text{Ag}, depositing dark metallic silver.

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Cloud Seeding

A weather modification technique in which microscopic silver iodide (AgI\text{AgI}) particles are sprayed into clouds to serve as artificial ice nuclei that stimulate snowfall or rain.

<p>A weather modification technique in which microscopic silver iodide ($$\text{AgI}$$) particles are sprayed into clouds to serve as artificial ice nuclei that stimulate snowfall or rain.</p>
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Polytetrafluoroethylene (PTFE)

A durable, low-friction synthetic fluoropolymer known commercially as Teflon, produced from fluorine compounds and used for non-stick cookware.

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Transition Element (IUPAC Definition)

An element whose ground-state neutral atom possesses an incomplete d-subshell, or an element that forms one or more stable cations with an incomplete d-subshell.

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d-Block Elements

Elements belonging to Groups 3 through 12 of the periodic table in which electrons progressively occupy the (n-1)d subshell.

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Non-Transition Status of Zinc

The formal exclusion of zinc from transition metals because its neutral atom ([Ar]3d104s2[\text{Ar}]3d^{10}4s^2) and only common cation (Zn2+:[Ar]3d10\text{Zn}^{2+}: [\text{Ar}]3d^{10}) contain completely filled d-subshells.

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Transition Metal Classification of Copper

The classification of copper as a transition element because its common Cu2+\text{Cu}^{2+} ion has an incompletely filled d-subshell ([Ar]3d9[\text{Ar}]3d^9), despite the neutral atom ([Ar]3d104s1[\text{Ar}]3d^{10}4s^1) having a full d-subshell.

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Aufbau Principle

The quantum mechanical rule stating that electrons fill lower-energy atomic orbitals before occupying higher-energy orbitals.

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Chromium Electron Configuration

The anomalous ground-state electron arrangement [Ar]3d54s1[\text{Ar}]3d^5 4s^1 instead of the expected [Ar]3d44s2[\text{Ar}]3d^4 4s^2, stabilized by the thermodynamic stability of a half-filled d-subshell.

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Copper Electron Configuration

The anomalous ground-state electron arrangement [Ar]3d104s1[\text{Ar}]3d^{10} 4s^1 rather than [Ar]3d94s2[\text{Ar}]3d^9 4s^2, favored due to the enhanced stability of a completely filled d-subshell.

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Palladium Electron Configuration

The anomalous ground-state arrangement of element 46 ([Kr]4d10[\text{Kr}]4d^{10}), where both 5s electrons reside in the 4d subshell to achieve a full set of ten d-electrons and zero s-electrons.

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Transition Metal Ionization Sequence

The order of electron removal during cation formation in which outer ns electrons (such as 4s) are removed before any inner (n-1)d electrons.

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Metallic Bonding in Transition Metals

Exceptionally strong lattice bonding resulting from the delocalization of both outer ns and inner (n-1)d electrons into a shared sea of communal electrons.

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Variable Oxidation States

The property of transition elements to display multiple oxidation numbers (from +2+2 up to +7+7 in the first series) because the energies of 4s and 3d electrons are close enough to allow both to participate in bonding.

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Transition Metal Oxide Acidity Trends

The chemical principle where low oxidation state transition metal oxides are basic and ionic (e.g., MnO\text{MnO}, FeO\text{FeO}), intermediate states are amphoteric (e.g., Cr2O3\text{Cr}_2\text{O}_3, MnO2\text{MnO}_2), and high oxidation states are acidic and covalent (e.g., CrO3\text{CrO}_3, Mn2O7\text{Mn}_2\text{O}_7).

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Catalyst

A substance that increases the rate of a chemical reaction without being consumed by providing an alternative reaction pathway with a lower activation energy (Ea′<EaE_a' < E_a).

<p>A substance that increases the rate of a chemical reaction without being consumed by providing an alternative reaction pathway with a lower activation energy ($$E_a' < E_a$$).</p>
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Haber Process Catalyst

Finely divided iron (Fe\text{Fe}), used as a heterogeneous catalyst to facilitate the industrial synthesis of ammonia (NH3\text{NH}_3) from nitrogen and hydrogen gases.

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Contact Process Catalyst

Vanadium pentoxide (V2O5\text{V}_2\text{O}_5), a transition metal compound used to catalyze the conversion of sulfur dioxide (SO2\text{SO}_2) to sulfur trioxide (SO3\text{SO}_3) in sulfuric acid manufacture.

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Alloy

A solid metallic solution formed by melting two or more metals of similar atomic radii together, such as steel (Fe+C\text{Fe} + \text{C}) or brass (Cu+Zn\text{Cu} + \text{Zn}), resulting in enhanced strength and corrosion resistance.

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Coordination Complex

A compound or ion in which a central metal cation is covalently coordinated to a group of surrounding anions or neutral molecules through dative bonds.

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Ligand

An anion or neutral molecule possessing at least one donor atom with a lone pair of electrons used to form a dative covalent bond with a central metal ion.

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d-d Electronic Transition

The excitation of an electron from a lower-energy d-orbital to a higher-energy d-orbital upon absorbing visible light, which imparts characteristic colours to transition metal complexes.