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Being a widely available reagent, TsCl has been heavily examined from the perspective of reactivity. It is used in dehydrations to make nitriles, isocyanides and diimides. [2] In an unusual reaction focusing on the sulfur center, zinc reduces TsCl to the sulfinate, CH 3 C 6 H 4 SO 2 Na. [4]
The transition state, represented by the double dagger symbol represents the exact configuration of atoms that has an equal probability of forming either the reactants or products of the given reaction. [5] The activation energy is the minimum amount of energy to initiate a chemical reaction and form the activated complex. [6]
Tosyl group (blue) with a generic "R" group attached Tosylate group with a generic "R" group attached. Note the extra oxygen, compared to plain tosyl. In organic chemistry, a toluenesulfonyl group (tosyl group, abbreviated Ts or Tos [nb 1]) is a univalent functional group with the chemical formula −SO 2 −C 6 H 4 −CH 3.
One of the most important features introduced by Eyring, Polanyi and Evans was the notion that activated complexes are in quasi-equilibrium with the reactants. The rate is then directly proportional to the concentration of these complexes multiplied by the frequency (k B T/h) with which they are converted into products. Below, a non-rigorous ...
The combination leads to a standard set of curves in which reaction progress is read from right to left along the x-axis and reaction rate is read from bottom to top along the y-axis. [2] While these plots often provide a visually compelling demonstration of basic kinetic trends, differential methods are generally superior for extracting ...
A reaction can also have an undefined reaction order with respect to a reactant if the rate is not simply proportional to some power of the concentration of that reactant; for example, one cannot talk about reaction order in the rate equation for a bimolecular reaction between adsorbed molecules:
where A and B are reactants C is a product a, b, and c are stoichiometric coefficients,. the reaction rate is often found to have the form: = [] [] Here is the reaction rate constant that depends on temperature, and [A] and [B] are the molar concentrations of substances A and B in moles per unit volume of solution, assuming the reaction is taking place throughout the volume of the ...
The one on the left is a bicyclo[2.2.2]octene, which, at 200 °C, extrudes ethylene in a retro-Diels–Alder reaction. Compared to the compound on the right (which, lacking an alkene group, is unable to give this reaction) the bridgehead carbon-carbon bond length is expected to be shorter if the theory holds, because on approaching the ...