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  2. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    the simple first-order rate law described in introductory textbooks. Under these conditions, the concentration of the nucleophile does not affect the rate of the reaction, and changing the nucleophile (e.g. from H 2 O to MeOH) does not affect the reaction rate, though the product is, of course, different. In this regime, the first step ...

  3. SN1CB mechanism - Wikipedia

    en.wikipedia.org/wiki/Sn1CB_mechanism

    The rate law for the reaction is: = [() +] [] The rate law is deceptive: hydroxide serves not as a nucleophile but as a base to deprotonate the coordinated ammonia. Simultaneously with deprotonation, the halide dissociates.

  4. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    The rate equation for this reaction would be Rate=k[Sub][Nuc]. For a S N 2 reaction, an aprotic solvent is best, such as acetone, DMF, or DMSO. Aprotic solvents do not add protons (H + ions) into solution; if protons were present in S N 2 reactions, they would react with the nucleophile and severely limit the reaction rate. Since this reaction ...

  5. Rate equation - Wikipedia

    en.wikipedia.org/wiki/Rate_equation

    In chemistry, the rate equation (also known as the rate law or empirical differential rate equation) is an empirical differential mathematical expression for the reaction rate of a given reaction in terms of concentrations of chemical species and constant parameters (normally rate coefficients and partial orders of reaction) only. [1]

  6. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    The two reactions are named according tho their rate law, with S N 1 having a first-order rate law, and S N 2 having a second-order. [2] S N 1 reaction mechanism occurring through two steps. The S N 1 mechanism has two steps. In the first step, the leaving group departs, forming a carbocation (C +). In the second step, the nucleophilic reagent ...

  7. SNi - Wikipedia

    en.wikipedia.org/wiki/SNi

    A typical representative organic reaction displaying this mechanism is the chlorination of alcohols with thionyl chloride, or the decomposition of alkyl chloroformates, the main feature is retention of stereochemical configuration. Some examples for this reaction were reported by Edward S. Lewis and Charles E. Boozer in 1952. [2]

  8. Is Enron back? If it's a joke, some former employees aren't ...

    www.aol.com/enron-back-joke-former-employees...

    An elaborate parody appears to be behind an effort to resurrect Enron, the Houston-based energy company that exemplified the worst in American corporate fraud and greed after it went bankrupt in 2001.

  9. Associative substitution - Wikipedia

    en.wikipedia.org/wiki/Associative_substitution

    The first step is typically rate determining. Thus, the entropy of activation is negative, which indicates an increase in order in the system. These reactions follow second order kinetics: the rate of the appearance of product depends on the concentration of MX 4 and Y. The rate law is governed by the Eigen–Wilkins Mechanism.