First Order Rate Equation:
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The first order rate constant (k) describes the rate of a first-order chemical reaction, where the reaction rate is directly proportional to the concentration of one reactant. It is a fundamental parameter in chemical kinetics.
The calculator uses the first order rate equation:
Where:
Explanation: The equation describes how the concentration of a reactant changes over time in a first-order reaction. The natural logarithm of the ratio of concentrations is proportional to the elapsed time.
Details: The rate constant is crucial for understanding reaction kinetics, predicting reaction progress, and designing chemical processes. It helps determine reaction half-life and is used in various fields including pharmaceuticals, environmental science, and materials engineering.
Tips: Enter concentrations in molarity (M) and time in seconds (s). All values must be positive numbers. The initial concentration should be greater than the final concentration for meaningful results.
Q1: What are typical units for first order rate constant?
A: The units are reciprocal time (1/s, 1/min, etc.). The calculator uses 1/s by default.
Q2: How does temperature affect the rate constant?
A: Rate constant increases with temperature, typically following the Arrhenius equation: \( k = Ae^{-E_a/RT} \).
Q3: What is the relationship between rate constant and half-life?
A: For first-order reactions: \( t_{1/2} = \ln(2)/k \). The half-life is constant and independent of initial concentration.
Q4: Can this be used for radioactive decay?
A: Yes, radioactive decay follows first-order kinetics, so this equation applies to decay rate calculations.
Q5: What if my final concentration is higher than initial?
A: This would give a negative rate constant, which is physically impossible for a first-order reaction. Check your measurements.