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  2. Molecularity - Wikipedia

    en.wikipedia.org/wiki/Molecularity

    Molecularity, on the other hand, is deduced from the mechanism of an elementary reaction, and is used only in context of an elementary reaction. It is the number of molecules taking part in this reaction. This difference can be illustrated on the reaction between nitric oxide and hydrogen: [11]

  3. Reaction mechanism - Wikipedia

    en.wikipedia.org/wiki/Reaction_mechanism

    An example of a simple chain reaction is the thermal decomposition of acetaldehyde (CH 3 CHO) to methane (CH 4) and carbon monoxide (CO). The experimental reaction order is 3/2, [4] which can be explained by a Rice-Herzfeld mechanism. [5] This reaction mechanism for acetaldehyde has 4 steps with rate equations for each step :

  4. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    In inorganic chemistry, the S N 1 reaction is often known as the dissociative substitution. This dissociation pathway is well-described by the cis effect. A reaction mechanism was first introduced by Christopher Ingold et al. in 1940. [3] This reaction does not depend much on the strength of the nucleophile, unlike the S N 2 mechanism. This ...

  5. Elementary reaction - Wikipedia

    en.wikipedia.org/wiki/Elementary_reaction

    In practice, a reaction is assumed to be elementary if no reaction intermediates have been detected or need to be postulated to describe the reaction on a molecular scale. [1] An apparently elementary reaction may be in fact a stepwise reaction, i.e. a complicated sequence of chemical reactions, with reaction intermediates of variable lifetimes.

  6. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    An example of a substitution reaction taking place by a so-called borderline mechanism as originally studied by Hughes and Ingold [6] is the reaction of 1-phenylethyl chloride with sodium methoxide in methanol. The reaction rate is found to the sum of S N 1 and S N 2 components with 61% (3,5 M, 70 °C) taking place by the latter.

  7. Rate-determining step - Wikipedia

    en.wikipedia.org/wiki/Rate-determining_step

    Another example is the unimolecular nucleophilic substitution (S N 1) reaction in organic chemistry, where it is the first, rate-determining step that is unimolecular. A specific case is the basic hydrolysis of tert-butyl bromide (t-C 4 H 9 Br) by aqueous sodium hydroxide. The mechanism has two steps (where R denotes the tert-butyl radical t-C ...

  8. Murai reaction - Wikipedia

    en.wikipedia.org/wiki/Murai_reaction

    A detailed mechanism for the Murai reaction has not been elucidated. Experimental and computational studies give evidence for at least two different mechanisms, depending on the catalyst . [ 10 ] [ 11 ] For catalysts such as [Ru(H) 2 (CO)(PR 3 ) 3 ] which are active as Ru 0 , a combination of computational density functional studies and ...

  9. Reaction rate constant - Wikipedia

    en.wikipedia.org/wiki/Reaction_rate_constant

    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 ...

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