Although only the net chemical change is directly observable for most chemical reactions, experiments that suggest the possible sequence of steps in a reaction mechanism can often be designed. Recently, electrospray ionization mass spectrometry has been used to corroborate the mechanism of several organic reaction proposals.
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 reactants used, the function of a catalyst, stereochemistry, all products 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 points on the potential energy surface for the reaction.
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.
Consider the following reaction:
- CO + NO2 → CO2 + NO
In this case, experiments have determined that this reaction takes place according to the rate law . This form suggests that the rate-determining step is a reaction between two molecules of NO2. A possible mechanism for the overall reaction that explains the rate law is:
- 2 NO2 → NO3 + NO (slow)
- NO3 + CO → NO2 + CO2 (fast)
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 NO2 molecules, it is a bimolecular reaction with a rate law of . 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.
There are also more complex mechanisms such as chain reactions, in which the propagation steps of the chain form a closed cycle.
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 experiments.
- 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.
In general, reaction steps involving more than three molecular entities do not occur.
- Organic reactions by mechanism under Organic reaction
- Nucleophilic acyl substitution
- Neighbouring group participation
- Finkelstein reaction
- Lindemann mechanism
- Electrochemical reaction mechanism
- Nucleophilic abstraction
- March, Jerry (1985), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (3rd ed.), New York: Wiley, ISBN 0-471-85472-7
- Investigation of chemical reactions in solution using API-MS 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