Chem 2 – Core Concepts & Vocabulary (Pre-Class Set)

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99 Terms

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Enthalpy (ΔH)

Heat content of a system at constant pressure

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Exothermic reaction

Reaction that releases heat to surroundings (ΔH < 0)

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Endothermic reaction

Reaction that absorbs heat from surroundings (ΔH > 0)

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Entropy (ΔS)

Measure of disorder or randomness in a system

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Second Law of Thermodynamics

Total entropy of the universe always increases

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Gibbs Free Energy (ΔG)

Energy available to do useful work

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Standard conditions

1 atm pressure, 1 M concentrations, 25°C

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State function

A property that depends only on initial and final states, not the reaction path.

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Hess’s Law

Overall enthalpy change equals sum of individual steps

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Reaction rate

Change in concentration of reactant or product per unit time

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Rate law

Mathematical expression relating rate to reactant concentrations

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Rate constant (k)

Proportionality constant in the rate law

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Reaction order

Power to which concentration is raised in the rate law

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Overall reaction order

Sum of individual reactant orders

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Elementary step

Single-step reaction in a mechanism

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Reaction mechanism

Sequence of elementary steps in a reaction

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Activation energy (Ea)

Minimum energy required for reaction to occur

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Catalyst

Substance that increases rate without being consumed

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Transition state

High-energy configuration between reactants and products

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First Law of Thermodynamics

Energy cannot be created or destroyed, only transferred or transformed.

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Equilibrium constant (K)

Ratio of product to reactant concentrations at equilibrium

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Reaction quotient (Q)

Same form as K but for non-equilibrium conditions

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Le Châtelier’s Principle

System shifts to counteract applied stress

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Homogeneous equilibrium

All species in same phase

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Heterogeneous equilibrium

Species in different phases

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Equilibrium position

Relative amounts of reactants and products at equilibrium

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Arrhenius acid

Substance that produces H⁺ in water

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Arrhenius base

Substance that produces OH⁻ in water

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Brønsted–Lowry acid

Proton (H⁺) donor

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Brønsted–Lowry base

Proton (H⁺) acceptor

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Conjugate acid

Species formed when a base gains a proton

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Conjugate base

Species formed when an acid loses a proton

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Lewis acid

Electron pair acceptor

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Lewis base

Electron pair donor

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Strong acid

Completely ionizes in water

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Weak acid

Partially ionizes in water

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pH

Measure of acidity based on hydrogen ion concentration

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pOH

Measure of basicity based on hydroxide ion concentration

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Autoionization of water

Water molecules react to form H⁺ and OH⁻

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Ion product of water (Kw)

Product of [H⁺][OH⁻] at equilibrium

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Buffer

Solution that resists changes in pH

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Common ion effect

Suppression of ionization due to shared ion

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Oxidation

Loss of electrons

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Reduction

Gain of electrons

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Redox reaction

Reaction involving electron transfer

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Anode

Electrode where oxidation occurs

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Cathode

Electrode where reduction occurs

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Galvanic cell

Cell that produces electrical energy from spontaneous reaction

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Electrolytic cell

Cell that uses electrical energy to drive reaction

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Cell potential

Measure of voltage produced by a cell

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Electronegativity

Ability of an atom to attract electrons

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Electronegativity difference (ΔEN)

Difference in electronegativity between bonded atoms

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Polar bond

Covalent bond with unequal electron sharing

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Nonpolar bond

Covalent bond with equal electron sharing

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Partial charge (δ⁺ / δ⁻)

Slight positive or negative charge in a polar bond

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Charge separation

Spatial separation of partial charges in a molecule

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Molecular polarity

Overall charge distribution of a molecule

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Molecular geometry

Three-dimensional arrangement of atoms

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Electron domain

Region of electron density around a central atom

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Symmetrical molecule

Shape where dipoles cancel

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Asymmetrical molecule

Shape where dipoles do not cancel

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Intermolecular forces (IMF)

Attractions between molecules

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Dipole–dipole forces

Attractions between polar molecules

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Hydrogen bonding

Strong dipole–dipole involving H bonded to N, O, or F

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London dispersion forces

Weak attractions from temporary dipoles

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Ion–dipole forces

Attraction between ion and polar molecule

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Spontaneous

Thermodynamically favored, not necessarily fast

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Dynamic equilibrium

Continuous forward and reverse reactions

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Work

energy transferred by force acting over a distance

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Heat

energy transferred due to a temperature difference

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Calorimetry

measurement of heat flow using temperature changes

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Standard enthalpy of formation

enthalpy change when 1 mole of a compound forms from its elements in their standard states

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Sigma Σ

sum of multiple terms

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Matter

Anything that has mass and occupies volume

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Pure substance

Matter with a fixed, definite composition

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Mixture

Physical combination of substances with variable composition

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Homogeneous mixture

Mixture with uniform composition throughout

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Heterogeneous mixture

Mixture with non-uniform composition

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Solution

Homogeneous mixture of solute dissolved in solvent

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Solvent

Substance that dissolves the solute

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Solute

Substance that is dissolved

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Aqueous

Dissolved in water

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Base unit of mass

gram (g)

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Base unit of length

meter (m)

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Base unit of volume

liter (L)

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Base unit of amount

mole (mol)

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Base unit of temperature

kelvin (K)

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kilo (k)

10³

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centi (c)

10⁻²

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milli (m)

10⁻³

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micro (µ)

10⁻⁶

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Kilogram to gram

1 kg = 1000 g

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Gram to milligram

1 g = 1000 mg

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Meter to centimeter

1 m = 100 cm

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Centimeter to millimeter

1 cm = 10 mm

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Kilometer to meter

1 km = 1000 m

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Liter to milliliter

1 L = 1000 mL

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Kilojoule to joule

1 kJ = 1000 J

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