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bond energy
the energy that is required to break chemical bonds
chemical bond
the force that holds atoms, molecules, or ions together to form chemical compounds
endothermic reaction
a chemical reaction that absorbs energy from the surrounding environment
enthalpy (H)
the sum of a system’s internal energy and the product of its pressure and volume
exothermic reaction
a chemical reaction that releases energy into the environment
law of conservation of energy
energy can be neither created nor destroyed, only transformed between forms (e.g., bond ↔ thermal)
ΔH (enthalpy change)
Hproducts − Hreactants; negative for exothermic, positive for endothermic
Hess’s law
total enthalpy change is the same whether a reaction occurs in one step or multiple steps
standard enthalpy of formation
ΔH when one mole of a compound forms from its elements in standard states
bond dissociation enthalpy
the energy required to homolytically cleave a bond, yielding radicals
system
the reactants and products in a chemical reaction being studied
surroundings
everything outside of that system
Additional/Internal
open vs. closed vs. isolated system
can exchange energy and/or matter differently
state function
property (e.g., enthalpy, internal energy) that depends only on the system’s state, not on how it got there
spontaneous process
occurs without outside intervention; indicated by ΔG < 0 under standard conditions
Gibbs free energy (G)
G
calorimeter
apparatus used to measure heat flow between the system and surroundings
chemical bond
an electrical force that holds the atoms of molecules together
bond energy
the energy required to break apart a chemical bond
activation energy (Eₐ)
minimum energy needed to initiate bond breaking in reactants
transition state
high‑energy, fleeting configuration at the top of the Eₐ hill
collision theory
molecules must collide with proper orientation and sufficient energy to react
reaction coordinate diagram
plots potential energy versus reaction progress, showing Eₐ and ΔH
catalyst
provides an alternative pathway with lower activation energy without being consumed
electronegativity
a measure of the ability of an atom to attract electrons to itself
chemical reaction system
the reactants and products in a particular reaction being studied
covalent bond
sharing of electron pairs between atoms
ionic bond
electrostatic attraction between oppositely charged ions
polar covalent bond
unequal sharing of electrons due to electronegativity difference
Lewis structure
diagram showing the arrangement of electrons in molecules
resonance
delocalization of electrons across adjacent bonds, lowering overall energy
conduction
the transfer of energy by direct contact
convection
the transfer of energy by currents of moving fluids
radiation
the transfer of energy as electromagnetic waves
endothermic reaction
a chemical reaction in which there is a net input of energy from the surroundings into the system
exothermic reaction
a chemical reaction in which there is a net output of energy from the system into the surroundings
kinetic energy (KE)
energy of motion
potential energy (PE)
energy due to position or composition
activation energy
the energy that must be added to a system to break the bonds of the reactants
thermochemistry
the study of energy changes in chemical and physical changes
Maxwell–Boltzmann distribution
statistical spread of molecular kinetic energies at a given T
degrees of freedom
translational, rotational, vibrational modes that contribute to KE
enthalpy vs. internal energy (U)
U = q + w; under constant pressure, ΔH = ΔU + PΔV
endotherm/exotherm on PE diagram
uphill vs. downhill net change in PE from reactants to products
heat (q) vs. work (w)
energy transfer as heat versus mechanical work
relative potential energy
the difference in potential energies of reactants and products that determines net energy change
ionic bond
the bond between oppositely charged ions in a compound
catalyst
a substance that speeds up a reaction by lowering activation energy
lattice energy
energy released when gaseous ions form an ionic solid; related to ionic bond strength
Born–Haber cycle
thermochemical cycle for calculating lattice energies via Hess’s law
bond order
number of shared electron pairs between two atoms; higher bond order → greater bond energy
Madelung constant
geometric factor in calculating lattice energy for ionic crystals
thermodynamic stability
lower PE species are more stable; exothermic formation → more stable products