General Chemistry: Solutions, States of Matter, Acids and Bases, Stoichiometry, Redox, and Gases

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Vocabulary practice flashcards covering fundamental chemistry topics including solution behavior, intermolecular forces and states of matter, acid-base theories, stoichiometry and yields, oxidation-reduction processes, and gas laws.

72 Terms

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Electrolyte

A material that dissolves in water to form a solution that conducts electricity, containing dissolved ions.

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Nonelectrolyte

A material that dissolves in water to form a solution that does not conduct electricity, consisting of intact dissolved neutral molecules.

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Dissociation

The physical process in which pre-existing ions in an ionic compound separate from each other when dissolved in a solvent.

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Ionization

The chemical process in which new ions are created from neutral molecules upon dissolving in a solvent.

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Precipitation Reaction

A reaction in which an insoluble solid (precipitate) forms upon mixing two aqueous solutions via double replacement or metathesis.

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Spectator Ions

Ions in an ionic equation that do not participate directly in the chemical reaction and are eliminated to yield the net ionic equation.

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Net Ionic Equation

A chemical equation showing only the reacting species, written after eliminating spectator ions from the complete ionic equation.

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Intermolecular Forces

Attractive forces that exist among the particles that compose matter, controlling physical properties such as boiling and melting points, vapor pressures, and viscosities.

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Thermal Energy

The energy associated with the constant random motion of the atoms and molecules composing matter, which increases with increasing temperature.

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London Dispersion Forces

Intermolecular attractions between an instantaneous dipole and an induced dipole that are present in all atoms and molecules.

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Polarizability

The ease with which the electron cloud of an atom or molecule can distort in response to an instantaneous dipole.

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Dipole–Dipole Interactions

Attractive electrostatic forces between polar molecules in which the positive end of one permanent dipole is attracted to the negative end of a neighboring molecule.

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Hydrogen Bond

An unusually strong type of dipole–dipole attraction that occurs when hydrogen is directly bonded to highly electronegative nitrogen (NN), oxygen (OO), or fluorine (FF).

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Ion–Dipole Forces

Attractive forces existing between an ion and the oppositely charged partial dipole of a polar molecule, enabling ionic substances to dissolve in polar solvents.

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Surface Tension

The property of liquids resulting from a net inward force on surface molecules that minimizes surface area; quantitatively, the energy required to increase the surface area by a given amount.

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Viscosity

The resistance of a liquid to flow, which increases with stronger intermolecular forces and decreases with higher temperatures.

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Capillary Action

The ability of a liquid to flow against gravity up a narrow tube due to a combination of cohesive forces within the liquid and adhesive forces to the tube surface.

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Cohesive Forces

The intermolecular attractive forces between like molecules within a liquid.

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Adhesive Forces

The attractive forces between unlike molecules, such as between liquid molecules and the surface of a container.

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Meniscus

The curving of a liquid surface in a thin tube caused by the competition between adhesive forces and cohesive forces.

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Boiling Point

The temperature at which a liquid's vapor pressure equals the external pressure, allowing vapor bubbles to form throughout the liquid.

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Normal Boiling Point

The temperature at which the vapor pressure of a liquid equals exactly 1 atm1\,\text{atm}.

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Sublimation

The endothermic phase transition in which surface molecules of a solid acquire sufficient energy to break free directly into the gas phase.

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Deposition

The exothermic phase transition in which gas/vapor molecules are captured directly into a solid.

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Heat of Fusion

The amount of energy required to change a solid at its melting point into a liquid.

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Heat of Vaporization

The amount of energy required to change a liquid at its boiling point into a gas.

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Heat of Sublimation

The amount of energy required to change a solid directly into a gas.

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Arrhenius Acid

A substance that increases the concentration of hydronium/hydrogen ions (H+H^+) when dissolved in water.

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Arrhenius Base

A substance that increases the concentration of hydroxide ions (OH−OH^-) when dissolved in water.

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Hydronium Ion

The complex ion (H3O+H_3O^+) formed when a highly reactive stripped proton (H+H^+) bonds with a water molecule.

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Brønsted–Lowry Acid

A proton (H+H^+) donor in a chemical reaction.

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Brønsted–Lowry Base

A proton (H+H^+) acceptor in a chemical reaction.

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Amphoteric Substance

A species that can act as either an acid or a base because it possesses both a transferable H+H^+ and an atom with a lone electron pair.

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Conjugate Acid–Base Pair

Two substances related to each other by the transfer of a single hydrogen ion (H+H^+); the species containing one more HH is always the acid.

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Acid–Base Indicators

Substances, such as natural plant dyes (anthocyanins) or litmus, that change colors depending on whether they are in acidic or basic solutions.

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Polyprotic Acid

An acid containing more than one ionizable proton (H+H^+) that loses them sequentially in stepwise ionization reactions.

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Acid Ionization Constant (KaK_a)

The equilibrium constant for the ionization reaction of a weak acid in water, where a larger value signifies a stronger acid.

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Base Ionization Constant (KbK_b)

The equilibrium constant for the reaction of a weak base with water to form OH−OH^- and its conjugate acid, defined as Kb=[OH−][H:Base+][:Base]K_b = \frac{[OH^-][H:\text{Base}^+]}{[:\text{Base}]}.

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Autoionization of Water

The process in which water molecules react with one another to produce hydronium and hydroxide ions according to H2O+H2O⇌H3O++OH−H_2O + H_2O \rightleftharpoons H_3O^+ + OH^-.

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Ion Product Constant of Water (KwK_w)

The product of the hydronium and hydroxide ion concentrations in water, equal to [H3O+][OH−]=1.00×10−14[H_3O^+][OH^-] = 1.00 \times 10^{-14} at 25 ∘C25\,^{\circ}\text{C}.

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pH

A logarithmic measure of solution acidity defined as pH=−log⁡[H3O+]\text{pH} = -\log[H_3O^+], where a values below 77 are acidic and above 77 are basic at 25 ∘C25\,^{\circ}\text{C}.

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pOH

A logarithmic measure of hydroxide concentration defined as pOH=−log⁡[OH−]\text{pOH} = -\log[OH^-], related to pH at 25 ∘C25\,^{\circ}\text{C} by pH+pOH=14.00\text{pH} + \text{pOH} = 14.00.

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Lewis Acid

An electron-pair acceptor; an electron-deficient species (electrophile) capable of forming a covalent bond.

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Lewis Base

An electron-pair donor; an electron-rich species (nucleophile) possessing a lone pair of electrons available for bonding.

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Chemistry

The study of the composition, structure, properties, and reactions of matter and the changes it undergoes.

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Stoichiometry

The numerical relationship and quantitative study between chemical quantities of reactants and products in a balanced chemical reaction.

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Limiting Reactant

The reactant that is completely consumed first in a chemical reaction, thereby limiting the maximum amount of product that can be formed.

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Excess Reactant

Any reactant that remains unreacted when the limiting reactant is completely used up and the reaction stops.

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Theoretical Yield

The maximum amount of product that would result if all of the limiting reactant reacted completely.

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Actual Yield

The amount of product actually isolated or obtained from an experimental chemical reaction.

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Percent Yield

The ratio of actual yield to theoretical yield multiplied by 100%, calculated as Percent Yield=Actual YieldTheoretical Yield×100%\text{Percent Yield} = \frac{\text{Actual Yield}}{\text{Theoretical Yield}} \times 100\%.

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Solution

A homogeneous mixture of two or more substances consisting of a solute dissolved uniformly in a solvent.

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Solute

The component of a solution that is dissolved and typically present in the smaller quantity.

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Solvent

The component of a solution that dissolves the solute, identified as the component present in the greatest quantity.

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Molarity (MM)

A unit of solution concentration defined as the number of moles of solute dissolved per one liter of solution (Molarity=moles of soluteliters of solution\text{Molarity} = \frac{\text{moles of solute}}{\text{liters of solution}}).

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Oxidation–Reduction (Redox) Reactions

Reactions in which electrons are transferred between reactants, resulting in changes in the oxidation states of atoms.

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Oxidation

The loss of electrons during a chemical process, manifested as an increase in the oxidation state of an atom.

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Reduction

The gain of electrons during a chemical process, manifested as a decrease in the oxidation state of an atom.

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Oxidizing Agent

The substance that causes oxidation in another species by gaining electrons, undergoing reduction in the process.

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Reducing Agent

The substance that causes reduction in another species by losing electrons, undergoing oxidation in the process.

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Oxidation State

A theoretical positive or negative integer assigned to an atom according to hierarchical rules to quantify its degree of electron gain or loss.

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Combustion Reaction

A chemical reaction in which a substance reacts rapidly with O2O_2, forming oxygen-containing compounds (such as CO2CO_2 and H2OH_2O) and releasing heat.

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Atmospheric Pressure

The pressure exerted by the column of air in Earth's atmosphere, which at sea level equals 1 atm1\,\text{atm} or 760 mmHg760\,\text{mmHg}.

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Barometer

An instrument used to measure atmospheric pressure by balancing the atmospheric force against a column of liquid mercury (HgHg).

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Manometer

A device used to measure experimental gas pressures, constructed as either an open-tube or closed-tube column containing liquid mercury.

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Boyle's Law

A gas law stating that for a fixed amount of gas at constant temperature, volume is inversely proportional to pressure (P1V1=P2V2P_1V_1 = P_2V_2).

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Charles's Law

A gas law stating that for a fixed amount of gas at constant pressure, volume is directly proportional to absolute temperature in kelvins (V1T1=V2T2\frac{V_1}{T_1} = \frac{V_2}{T_2}).

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Avogadro's Law

A gas law stating that at constant temperature and pressure, the volume of a gas is directly proportional to the number of moles of gas present (V1n1=V2n2\frac{V_1}{n_1} = \frac{V_2}{n_2}).

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Ideal Gas

A hypothetical gas that obeys the ideal gas law (PV=nRTPV = nRT) whose particles experience no intermolecular attractions or repulsions and possess negligible particle volume compared to the container.

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Standard Temperature and Pressure (STP)

The reference state defined as 0 ∘C0\,^{\circ}\text{C} (273.15 K273.15\,\text{K}) and 1 atm1\,\text{atm}, at which 1 mol1\,\text{mol} of an ideal gas occupies 22.414 L22.414\,\text{L}.

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Dalton's Law of Partial Pressures

The principle stating that the total pressure of a mixture of gases is equal to the sum of the partial pressures that each constituent gas would exert alone (Ptotal=P1+P2+P3+…P_{\text{total}} = P_1 + P_2 + P_3 + \dots).

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Mole Fraction (XiX_i)

The ratio of the number of moles of a specific component (nin_i) to the total number of moles of all components (nTn_T) in a mixture (Xi=ninTX_i = \frac{n_i}{n_T}).