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Related Concept Videos

Reversible or Opposing Reactions01:26

Reversible or Opposing Reactions

Reversible or opposing reactions play a crucial role in understanding the dynamic nature of chemical processes. While kinetics focuses on how reactions proceed, thermodynamics emphasizes that most reactions do not reach completion. Instead, a reverse reaction starts occurring over time, and when its rate equals that of the forward reaction, a dynamic equilibrium is established.For example, consider a simple chemical process where A forms B reversibly. The rate constants for the forward and...
Consecutive Reactions01:22

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Consecutive reactions involve a sequence where the product of a preceding reaction becomes the reactant for the subsequent one. In a simple scheme, A transforms into B, which further reacts to form C, with rate constants k1 and k2, respectively. This concept is evident in the radioactive decay series. Assuming an initial state with only A present, the conservation of matter leads to three coupled differential equations, determining the concentrations of A, B, and C over time.The rate of change...
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Chemical reactions often occur in a stepwise fashion involving two or more distinct reactions taking place in a sequence. A balanced equation indicates the reacting species and the product species, but it reveals no details about how the reaction occurs at the molecular level. The reaction mechanism (or reaction path) provides details regarding the precise, step-by-step process by which a reaction occurs. Each of the steps in a reaction mechanism is called an elementary reaction. These...
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The rate-determining step, or RDS, in a chemical reaction is the slowest step that determines the overall reaction rate. It is identified by using the observed rate law and typically involves approximation methods like the RDS approximation or the steady-state approximation.In the RDS approximation, also known as the rate-limiting-step or equilibrium approximation, the reaction mechanism consists of one or more reversible reactions near equilibrium, followed by a slower RDS, and then one or...
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For instance, the decomposition of ozone appears to follow a mechanism with two steps:
Reaction Quotient02:35

Reaction Quotient

The status of a reversible reaction is conveniently assessed by evaluating its reaction quotient (Q). For a reversible reaction described by m A + n B ⇌ x C + y D, the reaction quotient is derived directly from the stoichiometry of the balanced equation as

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Related Experiment Video

Updated: Jul 4, 2026

Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
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Published on: September 26, 2016

Reaction-subdiffusion equations for the A<=>B reaction.

F Sagués1, V P Shkilev, I M Sokolov

  • 1Departament de Química Física, Universitat de Barcelona, Martí i Franquès 1, E-08028 Barcelona, Spain.

Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|June 4, 2008
PubMed
Summary

This study explores a reversible reaction A <=> B under subdiffusion using continuous time random walks (CTRW). The reaction-subdiffusion equations show an unusual coupling between reactant concentrations, reflecting memory effects inherent in subdiffusion processes.

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Area of Science:

  • Chemical kinetics
  • Statistical physics
  • Anomalous transport phenomena

Background:

  • Subdiffusion processes are common in complex systems.
  • Continuous Time Random Walks (CTRW) model anomalous diffusion.
  • Linear reversible reactions are fundamental chemical processes.

Purpose of the Study:

  • To investigate reaction-subdiffusion dynamics for a linear reversible isomerization.
  • To derive and analyze the mesoscopic reaction-subdiffusion equations.
  • To understand the implications of subdiffusion on reaction kinetics.

Main Methods:

  • Modeling a linear reversible isomerization reaction (A <=> B).
  • Employing Continuous Time Random Walks (CTRW) to describe subdiffusion.
  • Deriving mesoscopic reaction-subdiffusion equations.

Main Results:

  • The derived equations exhibit an unusual coupling: the rate of change of A depends on both A and B concentrations.
  • This coupling arises from the memory effects in subdiffusion, where flux depends on past concentrations.
  • The CTRN framework reveals how particle history influences reaction dynamics.

Conclusions:

  • Subdiffusion significantly alters reaction dynamics compared to normal diffusion.
  • The derived reaction-subdiffusion equations capture the non-Markovian nature of the process.
  • This work provides insights into reaction kinetics in complex, heterogeneous environments.