First order reaction
First Order Reaction
A first order reaction is a type of chemical reaction where the rate of reaction is directly proportional to the concentration of one reactant. This means that the reaction rate depends linearly on the concentration of a single reactant raised to the first power. First order reactions are common in chemical kinetics and are characterized by a specific rate law and integrated rate equation.
Rate Law[edit | edit source]
For a first order reaction, the rate law can be expressed as:
- \( \text{Rate} = k[A] \)
where:
- \( k \) is the rate constant,
- \( [A] \) is the concentration of the reactant A.
The units of the rate constant \( k \) for a first order reaction are \( \text{s}^{-1} \).
Integrated Rate Equation[edit | edit source]
The integrated rate equation for a first order reaction is derived by integrating the rate law. It is given by:
- \( [A] = [A]_0 e^{-kt} \)
or in logarithmic form:
- \( \ln[A] = \ln[A]_0 - kt \)
where:
- \( [A]_0 \) is the initial concentration of the reactant,
- \( t \) is the time,
- \( e \) is the base of the natural logarithm.
This equation shows that the natural logarithm of the concentration of the reactant decreases linearly with time.
Half-Life[edit | edit source]
The half-life of a first order reaction, denoted as \( t_{1/2} \), is the time required for the concentration of the reactant to decrease to half of its initial value. For a first order reaction, the half-life is independent of the initial concentration and is given by:
- \( t_{1/2} = \frac{0.693}{k} \)
This property makes first order reactions particularly simple to analyze.
Examples[edit | edit source]
First order reactions are common in both chemical and biological systems. Some examples include:
- Radioactive decay of isotopes, where the rate of decay is proportional to the number of undecayed nuclei.
- The hydrolysis of aspirin in water.
- The decomposition of hydrogen peroxide in the presence of a catalyst.
Graphical Representation[edit | edit source]
In a plot of \( \ln[A] \) versus time \( t \), a first order reaction will yield a straight line with a slope of \( -k \). This linear relationship is a key diagnostic feature of first order kinetics.
Also see[edit | edit source]
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