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Transition State Theory
In chemistry, transition state theory (TST) explains the reaction rates of elementary chemical reactions. The theory assumes a special type of chemical equilibrium (quasi-equilibrium) between reactants and activated transition state complexes. TST is used primarily to understand qualitatively how chemical reactions take place. TST has been less successful in its original goal of calculating absolute reaction rate constants because the calculation of absolute reaction rates requires precise knowledge of potential energy surfaces, but it has been successful in calculating the standard enthalpy of activation (Δ''H''‡, also written Δ‡''H''ɵ), the standard entropy of activation (Δ''S''‡ or Δ‡''S''ɵ), and the standard Gibbs energy of activation (Δ''G''‡ or Δ‡''G''ɵ) for a particular reaction if its rate constant has been experimentally determined. (The ‡ notation refers to the value of interest ''at the transition state''; Δ''H''‡ is the difference between the ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Reactive Intermediate
In chemistry, a reactive intermediate or an intermediate is a short-lived, high-energy, highly reactive molecule. When generated in a chemical reaction, it will quickly convert into a more stable molecule. Only in exceptional cases can these compounds be isolated and stored, e.g. low temperatures, matrix isolation. When their existence is indicated, reactive intermediates can help explain how a chemical reaction takes place. Most chemical reactions take more than one elementary step to complete, and a reactive intermediate is a high-energy, yet stable, product that exists only in one of the intermediate steps. The series of steps together make a reaction mechanism. A reactive intermediate differs from a reactant or product or a simple reaction intermediate only in that it cannot usually be isolated but is sometimes observable only through fast spectroscopic methods. It is stable in the sense that an elementary reaction forms the reactive intermediate and the elementary reaction ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Kinetic Theory Of Gases
Kinetic (Ancient Greek: κίνησις “kinesis”, movement or to move) may refer to: * Kinetic theory, describing a gas as particles in random motion * Kinetic energy, the energy of an object that it possesses due to its motion Art and entertainment * Kinetic art, a form of art involving mechanical and/or random movement, including optical illusions. * ''Kinetic'', the 13th episode of the first season of the TV series ''Smallville'' * ''Kinetic'' (comics), a comic by Allan Heinberg and Kelley Pucklett * "Kinetic" (song), a song by Radiohead Companies * Kinetic Engineering Limited, Indian automotive manufacturer * Kinetic Group, Australian-based public transport company Technology * "Kinetic", Seiko's trademark for its automatic quartz technology * The ''Kinetic camera system'' by Birt Acres (1854–1918), photographer and film pioneer * Kinetic projectile Military terminology * Kinetic military action See also * * * Kinetics (other) * Dynamics (disambiguatio ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Collision Theory
Collision theory is a principle of chemistry used to predict the rates of chemical reactions. It states that when suitable particles of the reactant hit each other with correct orientation, only a certain amount of collisions result in a perceptible or notable change; these successful changes are called successful collisions. The successful collisions must have enough energy, also known as activation energy, at the moment of impact to break the pre-existing bonds and form all new bonds. This results in the products of the reaction. Increasing the concentration of the reactant brings about more collisions and hence more successful collisions. Increasing the temperature increases the average kinetic energy of the molecules in a solution, increasing the number of collisions that have enough energy. Collision theory was proposed independently by Max Trautz in 1916 and William Lewis in 1918. When a catalyst is involved in the collision between the reactant molecules, less energy is ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
William Lewis (chemist)
William Henry Lewis (1869 – 25 May 1963) was Professor of Chemistry at the University of Exeter for more than 30 years. Lewis was educated at University College of Wales, Aberystwyth (as it was then known) and Jesus College, Oxford. After graduating, he was a science teacher at Exeter School for seven years, before being appointed Professor of Chemistry at University College, Exeter (as it was then known) in 1901. From 1925 until his retirement in 1935, he combined his position as Professor with that of Vice-Principal of the College, helping to publicise the institution throughout Devon. In his role as Professor, he was regarded as having built up the Chemistry department from nothing into a "strong and vital unit." He served on the council of the Royal Institute of Chemistry The Royal Institute of Chemistry was a British scientific organisation. Founded in 1877 as the Institute of Chemistry of Great Britain and Ireland (ICGBI), its role was to focus on qualifications and ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Max Trautz
Max Trautz (19 March 1880 – 19 August 1960) was a German chemist. He was very productive with over 190 scientific publications especially in the field of chemical kinetics. He was the first to investigate the activation energy of molecules by connecting Max Planck's new results concerning light with observations in chemistry. He is also known as the founder of collision theory together with the British scientist William Lewis William or Willie Lewis may refer to: Politicians * William Lewis (MP for Anglesey) (by 1526–1601 or later), MP for Anglesey in 1553 and 1555 * William Lewis (MP for Helston), MP for Helston in 1584 * William Lewis (MP for King's Lynn) (died 15 .... While Trautz published his work in 1916, Lewis published it in 1918. However, they were unaware of each other's work due to World War I.Laidler, Keith James. The World of Physical Chemistry, Oxford University Press, 1993 Publications * Trautz, Max. ''Der Temperaturkoeffizient der spezifischen Wär ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
René Marcelin
René Marcelin (12 June 1885 – 24 September 1914) was a French physical chemist, who died in World War I at a young age. He was a pupil of Jean Baptiste Perrin at the Faculty of Sciences in Paris and performed theoretical studies in the field of chemical kinetics. Work René Marcelin developed the first theoretical treatment of the rate of chemical reactions that goes beyond a simple empirical description. He showed that the expression of the rate constant given by the Arrhenius equation had to be composed of two terms. In addition to the activation energy term, he considered that there had to be an activation entropy term. In 1910, Rene Marcelin introduced the concept of standard Gibbs energy of activation. In 1912, he treated the progress of a chemical reaction as a motion of a point in phase space In dynamical system theory, a phase space is a space in which all possible states of a system are represented, with each possible state corresponding to one uniq ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Svante Arrhenius
Svante August Arrhenius ( , ; 19 February 1859 – 2 October 1927) was a Swedes, Swedish scientist. Originally a physicist, but often referred to as a chemist, Arrhenius was one of the founders of the science of physical chemistry. He received the Nobel Prize for Chemistry in 1903, becoming the first Sweden, Swedish Nobel laureate. In 1905, he became director of the Nobel Institute, where he remained until his death."Arrhenius, Svante August" in ''Chambers's Encyclopædia''. London: George Newnes Ltd, George Newnes, 1961, Vol. 1, p. 635. Arrhenius was the first to use principles of physical chemistry to estimate the extent to which increases in atmospheric carbon dioxide are responsible for the Earth's increasing surface temperature. His work played an important role in the emergence of modern climate science. In the 1960s, Charles David Keeling demonstrated that the quantity of human-caused carbon dioxide emissions into the air is enough to cause global warming. The Arrhenius ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Thermodynamic Temperature
Thermodynamic temperature is a quantity defined in thermodynamics as distinct from kinetic theory or statistical mechanics. Historically, thermodynamic temperature was defined by Kelvin in terms of a macroscopic relation between thermodynamic work and heat transfer as defined in thermodynamics, but the kelvin was redefined by international agreement in 2019 in terms of phenomena that are now understood as manifestations of the kinetic energy of free motion of microscopic particles such as atoms, molecules, and electrons. From the thermodynamic viewpoint, for historical reasons, because of how it is defined and measured, this microscopic kinetic definition is regarded as an "empirical" temperature. It was adopted because in practice it can generally be measured more precisely than can Kelvin's thermodynamic temperature. A thermodynamic temperature reading of zero is of particular importance for the third law of thermodynamics. By convention, it is reported on the ''Kelvin scale'' ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Universal Gas Constant
The molar gas constant (also known as the gas constant, universal gas constant, or ideal gas constant) is denoted by the symbol or . It is the molar equivalent to the Boltzmann constant, expressed in units of energy per temperature increment per amount of substance, i.e. the pressure–volume product, rather than energy per temperature increment per ''particle''. The constant is also a combination of the constants from Boyle's law, Charles's law, Avogadro's law, and Gay-Lussac's law. It is a physical constant that is featured in many fundamental equations in the physical sciences, such as the ideal gas law, the Arrhenius equation, and the Nernst equation. The gas constant is the constant of proportionality that relates the energy scale in physics to the temperature scale and the scale used for amount of substance. Thus, the value of the gas constant ultimately derives from historical decisions and accidents in the setting of units of energy, temperature and amount of substanc ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Equilibrium Constant
The equilibrium constant of a chemical reaction is the value of its reaction quotient at chemical equilibrium, a state approached by a dynamic chemical system after sufficient time has elapsed at which its composition has no measurable tendency towards further change. For a given set of reaction conditions, the equilibrium constant is independent of the initial analytical concentrations of the reactant and product species in the mixture. Thus, given the initial composition of a system, known equilibrium constant values can be used to determine the composition of the system at equilibrium. However, reaction parameters like temperature, solvent, and ionic strength may all influence the value of the equilibrium constant. A knowledge of equilibrium constants is essential for the understanding of many chemical systems, as well as biochemical processes such as oxygen transport by hemoglobin in blood and acid–base homeostasis in the human body. Stability constants, formation cons ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Van 't Hoff Equation
The Van 't Hoff equation relates the change in the equilibrium constant, , of a chemical reaction to the change in temperature, ''T'', given the standard enthalpy change, , for the process. It was proposed by Dutch chemist Jacobus Henricus van 't Hoff in 1884 in his book ''Études de Dynamique chimique'' (''Studies in Dynamic Chemistry''). The Van 't Hoff equation has been widely utilized to explore the changes in state functions in a thermodynamic system. The Van 't Hoff plot, which is derived from this equation, is especially effective in estimating the change in enthalpy and entropy of a chemical reaction. Equation Summary and Uses The standard pressure, P^0, is used to define the reference state for the Van 't Hoff equation, which is where denotes natural logarithm, K_ is the thermodynamic equilibrium constant, and is the ideal gas constant. This equation is exact at any one temperature and all pressures, derived from the requirement that the Gibbs free en ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
