Category
page 1Chemical kinetics

half-life
{| class="wikitable" align=right
! Half-liveselapsed !! Fractionremaining !! colspan=2| Percentageremaining
|-
| 0 || ||align=right style="border-right-width: 0; padding-right:0"| 100||style="border-left-width: 0"|
|-
| 1 || ||align=right style="border-right-width: 0; padding-right:0"| 50||style="border-left-width: 0"|
|-
| 2 || ||align=right style="border-right-width: 0; padding-right:0"| 25||style="border-left-width: 0"|
|-
| 3 || ||align=right style="padding-right:0; border-right-width: 0"| 12||style="border-left-width: 0; padding-left:0"|.5
|-
| 4 || ||align=right style="border-right-width
catalysis
thumb|A range of industrial catalysts in pellet form
thumb|An air filter that uses a low-temperature oxidation catalyst to convert [[carbon monoxide to less toxic carbon dioxide at room temperature. It can also remove formaldehyde from the air.]]
Catalysis (, ) is the increase in rate of a chemical reaction due to an added substance known as a catalyst ( ). Catalysts are not consumed by the reaction and remain unchanged after the reaction. If the reaction is rapid and the catalyst is recycled quickly, a very small amount of catalyst often suffices; mixing, surface area, and temperature are imp
chemical kinetics
study of the rates of chemical reactions
activation energy
energy that must be input to a system to undergo a reaction or process

ribozyme
thumb|3D structure of a hammerhead ribozyme
chain reaction
sequence of reactions where a reactive product or by-product causes additional reactions to take place
reaction rate
for a reactant or product in a particular reaction is intuitively defined as how quickly or slowly a reaction takes place
Arrhenius equation
formula for the temperature dependence of reaction rates
reaction mechanism
any model explaining a chemical reaction
law of mass action
scientific law
transition state
set of states (each characterized by its own geometry, energy) in which an assembly of atoms, when randomly placed there, would have an equal probability of forming the reactants or of forming the products of that elementary reaction
Michaelis–Menten kinetics
Model of enzyme kinetics
elementary reaction
single-step chemical reaction
reaction intermediate
molecular entity that is formed from the reactants (or preceding intermediates) and reacts further to give the directly observed products of a chemical reaction
reaction rate constant
quantifies the rate of a chemical reaction
rate equation
equation that links reaction rate with concentrations of reactants in a chemical reaction
collision theory
kinetic theory of gases

molecularity
In chemistry, molecularity is the number of molecules that come together to react in an elementary (single-step) reaction and is equal to the sum of stoichiometric coefficients of reactants in the elementary reaction with effective collision (sufficient energy) and correct orientation.
Depending on how many molecules come together, a reaction can be unimolecular, bimolecular or even trimolecular.
rate-determining step
slowest step of reaction
limiting factor
bottleneck variable limiting the evolution of a system
reaction coordinate
abstract coordinate depicting chemical reaction progress
biochemical cascade
series of chemical reactions which are initiated by a stimulus acting on a receptor that is transduced to the cell interior through second messengers and ultimately to effector molecules, resulting in a cell response to the initial stimulus
transition state theory
scientific theory
activated complex
an arrangement of atoms in an arbitrary region near the saddle point of a potential energy surface
activation
In chemistry and biology, activation is the process whereby something is prepared or excited for a subsequent reaction.
Butler–Volmer equation
equation characterising electrochemical kinetics
Tafel equation
equation relating the rate of an electrochemical reaction to the overpotential
Eyring equation
equation used in chemical kinetics to describe changes in the rate of a chemical reaction with temperature
stabilizer
chemical that is used to prevent degradation
iodine clock reaction demonstration
chemical clock demonstration experiment
surface-area-to-volume ratio
relation between the surface area and the volume of an object
chemical clock
reaction that changes observably after a time
George S. Hammond
American chemist (1921–2005)

kinetic isotope effect
phenomenon in physical organic chemistry

pre-exponential factor
pre-exponential constant in the Arrhenius equation in Chemical Kinetics
detailed balance
term

multi-component reaction
chemical reaction where three or more compounds react to form a single product
Hammond's postulate
hypothesis in physical organic chemistry
steady state
central term in chemical kinetics
inelastic scattering
particle scattering in which kinetic energy is not conserved
Thorpe–Ingold effect
influence of substituents on the thermodynamics and kinetics of ring-closing reactions in organic chemistry
RRKM theory
Microcanonic transition state theory of unimolecular reactions
Acid catalysis
Chemical reaction
Deoxyribozyme
Deoxyribozymes, also called DNA enzymes, DNAzymes, or catalytic DNA, are DNA oligonucleotides that are capable of performing a specific chemical reaction, often but not always catalytic. This is similar to the action of other biological enzymes, such as proteins or ribozymes (enzymes composed of RNA).
However, in contrast to the abundance of protein enzymes in biological systems and the discovery of biological ribozymes in the 1980s,
there is only little evidence for naturally occurring deoxyribozymes.
Deoxyribozymes should not be confused with DNA aptamers which are oligonucleotides that sele
diffusion-controlled reaction
reaction rate equals rate of transport
Monod equation
Empirical model for microorganisms growth
Berry mechanism
type of pseudorotation in chemistry
Neighbouring group participation
intramolecular interaction
Stern–Volmer relationship
relationship describing the kinetics of intermolecular photochemical deactivation
Zel'dovich number
dimensionless parameter in fluid mechanics
stopped flow
Stopped-flow is one of a number of methods of studying the kinetics of reactions in solution. It is ideal for studying chemical reactions with a typical dead time on the order of 1 millisecond. In the simplest form of the technique, the solutions of two reactants are rapidly mixed by being forced through a mixing chamber, on emerging from which the mixed fluid passes through an optical observation cell. At some point in time, the flow is suddenly stopped, and the reaction is monitored using a suitable spectroscopic probe, such as absorbance, fluorescence or fluorescence polarization. The chang
reaction step
elementary reaction,stage of a stepwise reaction in which a reaction intermediate (reactants for the first step) is converted into the next reaction intermediate (products for the last step) in the sequence of intermediates between reactants/products
entropy of activation
Concept in chemical kinetics
Karlovitz number
dimensionless number used in chemical engineering
René Marcelin
French physical chemist
flash photolysis
technique for studying free-radical reactions in gases; an intense flash of light dissociates molecules in the sample creating free radicals, which can be detected spectroscopically
radical clock
chemical compound
Q10
temperature coefficient
Curtin–Hammett principle
Principle in chemical kinetics
Arrhenius plot
common linear graph used in chemical kinetics