Heat & Chemical Reactions Vocabulary

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Vocabulary flashcards defining fundamental concepts in thermodynamics, Gibbs free energy, and standard enthalpy changes.

Last updated 2:41 PM on 9/8/26
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29 Terms

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Universe

Everything that exists, possessing a total energy content that is constant and can neither be created nor destroyed.

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System

The specific part of the universe under study or observation.

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Surroundings

Everything outside the system but still considered part of the universe.

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Boundary

The separating surface that divides the system from its surroundings.

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Open System

A system that can exchange both mass and energy with its surroundings.

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Closed System

A system that can exchange energy with its surroundings, but cannot exchange mass.

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Isolated System

A system that exchanges neither mass nor energy with its surroundings.

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Thermodynamics

The branch of science that studies the relationship between heat and other forms of energy.

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Zeroth Law of Thermodynamics

States that if object AA is in thermal equilibrium with BB and BB is in thermal equilibrium with CC, then AA and CC are in thermal equilibrium and share the same temperature.

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First Law of Thermodynamics

States that energy can neither be created nor destroyed, only transformed from one form to another, represented by the formula ΔU=q+w\to \Delta U = q + w.

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Second Law of Thermodynamics

States that the total entropy of an isolated system always increases over time.

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Third Law of Thermodynamics

States that the entropy of a closed system at thermodynamic equilibrium approaches a constant value as temperature approaches absolute zero (0K0\,K).

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Intensive Properties

Properties unaffected by a change in the amount of matter, such as boiling point, melting point, density, and specific heat capacity.

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Extensive Properties

Properties affected by a change in the amount of matter, such as mass, volume, internal energy, heat capacity, and enthalpy change.

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Gibbs Free Energy (ΔG\Delta G)

The useful energy available to perform work, which determines the fate or spontaneity of a chemical reaction.

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Enthalpy Change (ΔH\Delta H)

The heat content of a reaction, representing the amount of heat absorbed or liberated.

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Entropy Change (ΔS\Delta S)

The measure of the change in the degree of disorderliness or randomness of a reaction.

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Entropy Jump

A phenomenon where a physical phase transition is directly bypassed, such as in sublimation where a solid transitions straight into a gas.

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Faraday's Constant (FF)

The physical constant representing the charge per mole of electrons, equal to 96485Cmol196485\,C\,mol^{-1}.

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Bond Energy

The average energy needed to break 1mole1\,mole of a chemical bond in its gaseous state.

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Glass Calorimeter

A simple and inexpensive instrument commonly used to measure the heat of chemical reactions.

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Bomb Calorimeter

A highly sensitive reaction vessel mainly used to measure the heat of combustion and analyze the energy content of food.

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Standard Enthalpy of Formation (ΔHf\Delta H^\circ_f)

The heat change when 1mole1\,mole of a substance is formed from its constituent elements under standard conditions (298K298\,K and 1atm1\,atm).

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Standard Enthalpy of Combustion (ΔHc\Delta H^\circ_c)

The heat liberated when 1mole1\,mole of a substance is completely burned in oxygen under standard conditions, which is always exothermic (ΔHc<0\Delta H^\circ_c < 0).

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Standard Enthalpy of Solution (ΔHsol\Delta H^\circ_{sol})

The heat absorbed or evolved when 1mole1\,mole of a substance is completely dissolved in water.

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Lattice Energy

The endothermic process energy required to break down a solid solute into its individual ions during dissolution.

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Hydration Energy

The exothermic process energy liberated when separated solute ions become surrounded by water molecules during dissolution.

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Standard Enthalpy of Neutralization (ΔHneut\Delta H^\circ_{neut})

The heat released when 1mole1\,mole of H+H^+ reacts with 1mole1\,mole of OHOH^- to produce 1mole1\,mole of H2OH_2O, which equals 57.1kJmol1-57.1\,kJ\,mol^{-1} for strong acid-strong base reactions.

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Hess's Law

Also known as the law of constant heat summation, it states that the overall enthalpy change of a reaction is constant regardless of the route or number of steps taken.