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In [[chemistry]], a '''reaction mechanism''' is the step by step [[sequence]] of [[elementary reaction]]s by which overall [[chemical]] change occurs.<ref>{{JerryMarch}}</ref>  
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Although only the net chemical change is directly [[observation|observable]] for most [[chemical reaction]]s, [[experiment]]s can often be designed that suggest the possible sequence of steps in a reaction mechanism. Recently, [[electrospray ionization mass spectrometry]]<ref>Investigation of chemical reactions in solution using API-MS''
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Leonardo Silva Santos, Larissa Knaack, Jurgen O. Metzger [[Int. J. Mass Spectrom.]]; '''2005'''; 246 pp 84 - 104; (Review) {{doi|10.1016/j.ijms.2005.08.016}}</ref> has been used to corroborate the mechanism of several organic reaction proposals.
 
==Description==
A chemical mechanism describes in detail exactly what takes place at each stage of an overall chemical reaction (transformation). It also describes each [[reactive intermediate]], [[activated complex]], and [[transition state]], and which bonds are broken (and in what order), and which bonds are formed (and in what order). A complete mechanism must also account for all [[reactant]]s used, the function of a [[catalyst]], [[stereochemistry]], all [[Product (chemistry)|product]]s formed and the amount of each. It must also describe the relative rates of the reaction steps and the [[rate equation]] for the overall reaction.  Reaction intermediates are chemical species, often unstable and short-lived, which are not reactants or products of the overall chemical reaction, but are temporary products and reactants in the mechanism's reaction steps.  Reaction intermediates are often [[free radicals]] or [[ions]]. Transition states can be unstable intermediate molecular states even in the elementary reactions. Transition states are commonly molecular entities involving an unstable number of bonds and/or unstable geometry. They correspond to  maxima on the [[reaction coordinate]], and to [[saddle point]]s on the [[potential energy surface]] for the reaction.
[[Image:BromoethaneSN2reaction-small.png|thumb|center|540px|[[SN2 reaction|S<sub>N</sub>2 reaction]] mechanism.  Note the negatively charged [[transition state]] in brackets in which the central [[carbon atom]] in question shows five bonds, an unstable condition.]]
 
The [[Arrow pushing|electron or arrow pushing]] method is often used in illustrating a reaction mechanism; for example, see the illustration of the mechanism for [[benzoin condensation]] in the following examples section.  
 
A reaction mechanism must also account for the order in which molecules react. Often what appears to be a single step conversion is in fact a multistep reaction.
 
==Examples==
Consider the following reaction:
 
:CO + NO<sub>2</sub> &rarr; CO<sub>2</sub> + NO
 
In this case, it has been experimentally determined that this reaction takes place according to the [[rate law]] <math>r = k[NO_2]^2</math>. This form suggests that the [[rate-determining step]] is a reaction between two molecules of NO<sub>2</sub>. A possible mechanism for the overall reaction which explains the rate law is:
 
:2 NO<sub>2</sub> &rarr; NO<sub>3</sub> + NO (slow)
:NO<sub>3</sub> + CO &rarr; NO<sub>2</sub> + CO<sub>2</sub> (fast)
 
Each step is called an elementary step, and each has its own [[rate law]] and [[molecularity]]. The elementary steps should add up to the original reaction.
 
When determining the overall rate law for a reaction, the slowest step is the step that determines the reaction rate. Because the first step (in the above reaction) is the slowest step, it is the [[rate-determining step]]. Because it involves the collision of two NO<sub>2</sub> molecules, it is a bimolecular reaction with a rate law of <math>r = k[NO_2]^2</math>. If we were to cancel out all the molecules that appear on both sides of the reaction, we would be left with the original reaction.
 
Other reactions may have mechanisms of several consecutive steps. In [[organic chemistry]], one of the first reaction mechanisms proposed was that for the [[benzoin condensation]], put forward in 1903 by [[A. J. Lapworth]].
[[Image:Benzoin condensation2.png|center|thumb|700px|[[Benzoin condensation]] '''reaction mechanism'''. [[Cyanide]] ion (CN<sup>-</sup>) acts as a [[catalyst]] here, entering at the first step and leaving in the last step. Proton (H<sup>+</sup>) transfers occur at (i) and (ii).  The [[arrow pushing]] method is used in some of the steps to show where electron pairs go.]]
 
There are also more complex mechanisms such as [[Chain reaction#Chemical chain reactions|chain reactions]], in which the ''propagation'' steps of the chain form a closed cycle.
 
==Modeling==
A correct reaction mechanism is an important part of accurate [[predictive modeling]]. For many combustion and plasma systems, detailed mechanisms are not available or require development.  
 
Even when information is available, identifying and assembling the relevant data from a variety of sources, reconciling discrepant values and extrapolating to different conditions can be a difficult process without expert help. Rate constants or thermochemical data are often not available in the literature, so computational chemistry techniques or group-additivity methods must be used to obtain the required parameters.
 
At the different stages of a reaction mechanism's elaboration, appropriate methods must be used.  One approach can involve the use of [[crossover experiment (chemistry)|crossover experiments]].
 
==Molecularity==
{{main|molecularity}}
 
'''Molecularity''' in [[chemistry]] is the number of colliding [[molecular entity|molecular entities]] that are involved in a single [[reaction step]].
* A reaction step involving one molecular entity is called unimolecular.
* A reaction step involving two molecular entities is called bimolecular.
* A reaction step involving three molecular entities is called termolecular.
 
Reaction steps involving more than three molecular entities generally do not occur.
 
==See also==
*[[Organic reaction#Organic reactions by mechanism|Organic reactions by mechanism]] under [[Organic reaction]]
*[[Nucleophilic acyl substitution]]
*[[Neighbouring group participation]]
*[[Finkelstein reaction]]
*[[Lindemann mechanism]]
*[[Electrochemical reaction mechanism]]
*[[Nucleophilic abstraction]]
 
==References==
{{Reflist}}
 
{{Reaction mechanisms}}
 
[[Category:Chemical reactions|Mechanism]]
[[Category:Reaction mechanisms| ]]
[[Category:Chemical kinetics]]
[[Category:Chemical engineering]]
[[Category:Combustion]]

Latest revision as of 21:07, 1 November 2014

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