Glossary
- Page ID
- 279584
\( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)
\( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)
\( \newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\)
( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\)
\( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\)
\( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\)
\( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\)
\( \newcommand{\Span}{\mathrm{span}}\)
\( \newcommand{\id}{\mathrm{id}}\)
\( \newcommand{\Span}{\mathrm{span}}\)
\( \newcommand{\kernel}{\mathrm{null}\,}\)
\( \newcommand{\range}{\mathrm{range}\,}\)
\( \newcommand{\RealPart}{\mathrm{Re}}\)
\( \newcommand{\ImaginaryPart}{\mathrm{Im}}\)
\( \newcommand{\Argument}{\mathrm{Arg}}\)
\( \newcommand{\norm}[1]{\| #1 \|}\)
\( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\)
\( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\AA}{\unicode[.8,0]{x212B}}\)
\( \newcommand{\vectorA}[1]{\vec{#1}} % arrow\)
\( \newcommand{\vectorAt}[1]{\vec{\text{#1}}} % arrow\)
\( \newcommand{\vectorB}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)
\( \newcommand{\vectorC}[1]{\textbf{#1}} \)
\( \newcommand{\vectorD}[1]{\overrightarrow{#1}} \)
\( \newcommand{\vectorDt}[1]{\overrightarrow{\text{#1}}} \)
\( \newcommand{\vectE}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash{\mathbf {#1}}}} \)
\( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)
\( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)
\(\newcommand{\avec}{\mathbf a}\) \(\newcommand{\bvec}{\mathbf b}\) \(\newcommand{\cvec}{\mathbf c}\) \(\newcommand{\dvec}{\mathbf d}\) \(\newcommand{\dtil}{\widetilde{\mathbf d}}\) \(\newcommand{\evec}{\mathbf e}\) \(\newcommand{\fvec}{\mathbf f}\) \(\newcommand{\nvec}{\mathbf n}\) \(\newcommand{\pvec}{\mathbf p}\) \(\newcommand{\qvec}{\mathbf q}\) \(\newcommand{\svec}{\mathbf s}\) \(\newcommand{\tvec}{\mathbf t}\) \(\newcommand{\uvec}{\mathbf u}\) \(\newcommand{\vvec}{\mathbf v}\) \(\newcommand{\wvec}{\mathbf w}\) \(\newcommand{\xvec}{\mathbf x}\) \(\newcommand{\yvec}{\mathbf y}\) \(\newcommand{\zvec}{\mathbf z}\) \(\newcommand{\rvec}{\mathbf r}\) \(\newcommand{\mvec}{\mathbf m}\) \(\newcommand{\zerovec}{\mathbf 0}\) \(\newcommand{\onevec}{\mathbf 1}\) \(\newcommand{\real}{\mathbb R}\) \(\newcommand{\twovec}[2]{\left[\begin{array}{r}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\ctwovec}[2]{\left[\begin{array}{c}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\threevec}[3]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\cthreevec}[3]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\fourvec}[4]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\cfourvec}[4]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\fivevec}[5]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\cfivevec}[5]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\mattwo}[4]{\left[\begin{array}{rr}#1 \amp #2 \\ #3 \amp #4 \\ \end{array}\right]}\) \(\newcommand{\laspan}[1]{\text{Span}\{#1\}}\) \(\newcommand{\bcal}{\cal B}\) \(\newcommand{\ccal}{\cal C}\) \(\newcommand{\scal}{\cal S}\) \(\newcommand{\wcal}{\cal W}\) \(\newcommand{\ecal}{\cal E}\) \(\newcommand{\coords}[2]{\left\{#1\right\}_{#2}}\) \(\newcommand{\gray}[1]{\color{gray}{#1}}\) \(\newcommand{\lgray}[1]{\color{lightgray}{#1}}\) \(\newcommand{\rank}{\operatorname{rank}}\) \(\newcommand{\row}{\text{Row}}\) \(\newcommand{\col}{\text{Col}}\) \(\renewcommand{\row}{\text{Row}}\) \(\newcommand{\nul}{\text{Nul}}\) \(\newcommand{\var}{\text{Var}}\) \(\newcommand{\corr}{\text{corr}}\) \(\newcommand{\len}[1]{\left|#1\right|}\) \(\newcommand{\bbar}{\overline{\bvec}}\) \(\newcommand{\bhat}{\widehat{\bvec}}\) \(\newcommand{\bperp}{\bvec^\perp}\) \(\newcommand{\xhat}{\widehat{\xvec}}\) \(\newcommand{\vhat}{\widehat{\vvec}}\) \(\newcommand{\uhat}{\widehat{\uvec}}\) \(\newcommand{\what}{\widehat{\wvec}}\) \(\newcommand{\Sighat}{\widehat{\Sigma}}\) \(\newcommand{\lt}{<}\) \(\newcommand{\gt}{>}\) \(\newcommand{\amp}{&}\) \(\definecolor{fillinmathshade}{gray}{0.9}\)Words (or words that have the same definition) | The definition is case sensitive | (Optional) Image to display with the definition [Not displayed in Glossary, only in pop-up on pages] | (Optional) Caption for Image | (Optional) External or Internal Link | (Optional) Source for Definition |
---|---|---|---|---|---|
(Eg. "Genetic, Hereditary, DNA ...") | (Eg. "Relating to genes or heredity") | ![]() |
The infamous double helix | https://bio.libretexts.org/ | CC-BY-SA; Delmar Larsen |
Word(s) | Definition | Image | Caption | Link | Source |
---|---|---|---|---|---|
Adiabatic Process | A thermodynamic process in which no heat is exchanged between a system and its surroundings. | ||||
Activity | An effective concentration used in non-ideal solutions and gases to account for deviations from ideal behavior. | ||||
Avogadro’s Law | States that equal volumes of gases at the same temperature and pressure contain an equal number of molecules. | ||||
Born-Haber Cycle | A thermodynamic cycle used to calculate lattice energy in ionic solids. | ||||
Buffer | A solution that resists changes in pH when small amounts of acid or base are added. | ||||
Calorimetry | The measurement of heat flow in chemical reactions and physical changes. | ||||
Carnot Cycle | A theoretical thermodynamic cycle that describes the most efficient heat engine possible. | ||||
Chemical Potential | The change in a system’s Gibbs energy with the addition of a mole of a substance, at constant temperature and pressure. | ||||
Clapeyron Equation | Describes the relationship between pressure, temperature, and phase equilibrium. | ||||
Colligative Properties | Properties of solutions that depend on solute particle number rather than type, such as boiling point elevation. | ||||
Degree of Dissociation | The fraction of a dissolved substance that separates into ions in solution. | ||||
Electrochemical Cell | A system that generates electrical energy from chemical reactions. | ||||
Entropy | A measure of disorder or randomness in a system. | ||||
Enthalpy | The heat content of a system at constant pressure. | ||||
Equation of State | A mathematical equation that describes the state of matter under given conditions, such as the ideal gas law. | ||||
Fugacity | A corrected pressure term used to describe real gas behavior. | ||||
Free Energy, Gibbs Free Energy | A thermodynamic quantity used to predict whether a reaction is spontaneous at constant pressure and temperature. | ||||
Gibbs-Duhem Equation | Relates the chemical potentials of components in a mixture. | ||||
Graham’s Law of Effusion | States that the rate of effusion of a gas is inversely proportional to the square root of its molar mass. | ||||
Half-Life | The time required for half of a reactant to be consumed in a reaction. | ||||
Helmholtz Energy | A thermodynamic function that measures the work potential of a system at constant volume and temperature. | ||||
Ideal Gas Law | An equation describing the state of an ideal gas: PV=nRT. | ||||
Joule-Thomson Effect | Describes the temperature change of a real gas when it is expanded or compressed without heat exchange. | ||||
Kinetic Molecular Theory | A model that explains gas behavior based on particle motion and collisions. | ||||
Lattice Energy | The energy required to separate an ionic solid into its gaseous ions. | ||||
Le Chatelier’s Principle | States that a system at equilibrium will adjust to counteract applied changes. | ||||
Maxwell’s Relations | A set of thermodynamic equations derived from the symmetry of second derivatives of thermodynamic potentials. | ||||
Michaelis-Menten Mechanism | A model describing enzyme-catalyzed reactions. | ||||
Non-Ideal Solution | A solution that deviates from Raoult’s law due to intermolecular interactions. | ||||
Partial Molar Volume | The volume contribution of a component in a mixture. | ||||
Phase Diagram | A graphical representation of phase stability as a function of temperature and pressure. | ||||
Pressure Dependence of Gibbs Energy | Describes how Gibbs energy varies with pressure. | ||||
Raoult’s Law | States that the vapor pressure of a solvent is proportional to its mole fraction in solution. | ||||
Reaction Mechanism | A step-by-step description of how a chemical reaction occurs. | ||||
Reaction Rate | The speed at which reactants are converted to products. | ||||
Solubility | The ability of a substance to dissolve in a solvent. | ||||
Standard Reduction Potential | A measure of the tendency of a chemical species to gain electrons. | ||||
Steady-State Approximation | Assumes that the concentration of reaction intermediates remains constant over time. | ||||
Temperature Dependence of Equilibrium Constant | Describes how equilibrium constants change with temperature. | ||||
Transition State Theory | A model describing the high-energy transition state of a reaction. | ||||
Van ’t Hoff Equation | Relates temperature changes to equilibrium constant changes. | ||||
Volume Dependence of Helmholtz Energy | Explains how Helmholtz energy changes with volume variations. |