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Comprehensive flashcards covering atomic structure, periodic trends, chemical bonding, inter-molecular forces, kinetics, thermodynamics, and equilibrium based on lecture notes.
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Mass number
The sum of protons and neutrons in an atom (P+N).
Isotopes
Atoms of an element that have different numbers of neutrons.
Avogadro’s number
A constant represented by 6.022imes1023.
STP (Standard Temperature and Pressure)
Conditions defined as 1atm and 273K, where the molar volume of a gas is 22.4L/mol.
Molarity (M)
A measure of concentration defined as moles/L.
Empirical formula
The simplest ratio of elements in a chemical substance.
Coulomb’s Law
The electrostatic force given by the equation F=r2kq1q2.
Photoelectron Spectroscopy
A technique measuring energy in electronvolts (eV) where the incoming radiation energy equals the binding energy plus the kinetic energy of the ejected electron.
Aufbau principle
The rule stating that electrons fill the lowest energy subshells available first.
Pauli exclusion principle
The rule stating that two electrons in the same orbital cannot have the same spin.
Hund’s rule
The rule stating that electrons occupy empty subshells first.
Ionization energy
The amount of energy required to remove an electron from an atom.
Electronegativity
How strongly the nucleus of an atom attracts electrons of other atoms within a bond.
Electron affinity
The energy change that occurs when an electron is added to an atom in the gas state, usually appearing as an exothermic process.
Ionic bonds
Bonds formed when a cation gives up electrons completely to an anion, resulting in electrostatic attractions in a lattice structure.
Metallic bonds
A sea of electrons model where a positively charged core remains stationary while valence electrons are highly mobile.
Single bond
A bond consisting of one sigma bond (order 1), characterized by having the longest length and the least bond energy.
Triple bond
A bond consisting of one sigma and two pi bonds (order 3), characterized by being the shortest and having the greatest bond energy.
Resonance
The process of averaging together all possible bond orders for bond order calculations of a specific bond.
Formal charge
The number of valence electrons minus the assigned electrons (including one electron for each shared bond).
Dipole-dipole forces
Attractions between polar molecules where the positive end of one molecule is attracted to the negative end of another.
Hydrogen bonds
A strong type of dipole-dipole attraction occurring when hydrogen is attracted to an extremely electronegative element, specifically F, O, or N.
London dispersion forces (LDF)
Weak attractions present in all molecules due to the random motion of electrons creating instantaneous polarity.
Vapor pressure
The pressure exerted by molecules that escape IMF at the surface of a liquid; it is directly proportional to temperature and inversely proportional to IMF strength.
Beer’s Law
Defined by A=abc, showing a direct relationship between the concentration (c) and absorbance (A) of a solution.
Oxidation-reduction (redox) reaction
A reaction that involves changes in the oxidation state of the chemical species involved.
Rate law
The equation Rate=k[A]x[B]y[C]z, where the constant k is dependent only on temperature.
Activation energy (Ea)
The sufficient energy required for reactants to collide and successfully undergo a chemical reaction.
Reaction intermediates
Species that are produced during a reaction mechanism but are fully consumed and do not appear in the final balanced equation.
Catalyst
A substance that increases the reaction rate without being consumed by providing a pathway with a lower activation energy.
First Law of Thermodynamics
The law stating that energy can be neither created nor destroyed.
Enthalpy of formation ($\Delta H_f$)
The change in energy when one mole of a compound is formed from its pure component elements in their standard states.
Hess’s Law
A method of finding the overall ΔH by adding the enthalpy changes of individual reaction steps together.
Specific heat
The amount of heat required to raise the temperature of one gram of a substance by one degree C or K, used in the equation q=mcΔT.
Le Chatelier’s principle
The principle stating that a system at equilibrium will shift to favor products or reactants to counteract changes in concentration, pressure, or temperature.
Reaction quotient (Q)
A value calculated using initial molar concentrations or partial pressures, used to determine which direction a reaction must shift to reach equilibrium (K).
Solubility product (Ksp)
The equilibrium constant for the dissociation of a solid salt into its aqueous ions.
Strong acids
Acids that dissociate completely in water, leaving no tendency for a reverse reaction to occur.
Buffer
A solution of a weak acid or base and its conjugate salt that resists changes in pH when additional acid or base is added.
Entropy (S)
A measurement of the randomness or dispersion within a system.
Gibbs free energy ($\Delta G$)
Determined by ΔG=ΔH−T×ΔS; a negative value indicates the reaction is spontaneous or thermodynamically favored.
Galvanic cells
Also called voltaic cells, these use a favored redox reaction to generate a flow of current, with oxidation at the negative anode and reduction at the positive cathode.
Faraday’s Constant (F)
A value of 96500C/mol of electrons used in electrochemistry calculations.