reaction mechanism
When you write a chemical equation, you only see the starting materials on the left and the products on the right, like a before-and-after photo. But how did the atoms actually get from one picture to the other? A reaction mechanism is the slow-motion movie that fills in every frame in between: which bonds break, which bonds form, in what order, and how the electrons move at each instant.
Concretely, a mechanism breaks a reaction down into one or more elementary steps. Each step is a single, simple event, often involving just one or two molecules colliding and electrons shifting. Chemists draw this with curved arrows, where each arrow shows the movement of a pair of electrons, not the movement of an atom. Along the way the molecules may pass through short-lived, unstable species called reactive intermediates (such as carbocations or free radicals), which are real molecules but exist for only a fleeting moment before reacting on.
Mechanisms matter because they let you predict and control. If you understand why a reaction happens the way it does, you can predict the product, choose conditions to favor it, and explain odd results. A mechanism is a proposed model, supported by evidence like reaction rates, stereochemistry, and isotope effects; it is never seen directly, so it can be refined or overturned when new data appear. Two reactions with the same overall equation can run by completely different mechanisms.
The overall reaction CH3Br + OH- -> CH3OH + Br- looks like one event, but its mechanism is a single step: the OH- attacks carbon from behind while Br- leaves at the same moment, in one smooth motion (an SN2 step).
The one-line equation hides a precise dance of electrons that the mechanism makes visible.
A mechanism is an evidence-backed proposal, not a photograph; you cannot prove a mechanism is correct, only show it is consistent with all the data and that rivals are not.