Half Life of a Reaction
Imagine you have a pile of 1000 coins, and every minute, exactly half of the coins that are still there vanish. After one minute, 500 coins remain. After another minute, 250 remain. Then 125, then about 62, and so on. The time it takes for the pile to shrink from 1000 to 500 is the same as the time it takes to shrink from 500 to 250, or from 250 to 125. That constant time interval is the half life.
In chemistry, a reaction's half life (t1/2) is the time required for the concentration of a reactant to fall to exactly one-half of its initial value. It is a simple, intuitive way to describe how fast a reaction proceeds — the shorter the half life, the faster the reaction.
The Precise Definition
For any reaction, if you start with an initial concentration [A]0, the half life t1/2 is the time at which:
[A]=21[A]0
That is all. But here is the crucial point: the half life is not a universal constant — it depends on the order of the reaction. For different reaction orders, the half life behaves very differently.
Half Life for a First Order Reaction
For a first order reaction, the rate law is:
Rate=k[A]
The integrated rate equation is:
[A]=[A]0e−kt
Set [A]=21[A]0 and solve for t:
21[A]0=[A]0e−kt1/2
Cancel [A]0:
21=e−kt1/2
Take natural logarithms:
ln(21)=−kt1/2
−ln2=−kt1/2
t1/2=kln2=k0.693
t1/2=k0.693
This is the key result: for a first order reaction, the half life is independent of the initial concentration. Whether you start with 1 M or 0.001 M, the time to halve the concentration is exactly the same. This is a unique property of first order reactions — no other order behaves this way.
Why Does This Matter?
The constancy of t1/2 for first order reactions is what makes radioactive decay predictable. Carbon-14 dating works because the half life of 14C is always 5730 years, regardless of how much carbon is present. The same principle applies to many chemical reactions, especially decompositions and isomerisations.
For a first order reaction, if you know the half life, you can find the rate constant instantly: k=0.693/t1/2. This is often the fastest way to get k from experimental data.
Contrast with Other Orders
For a zero order reaction, the half life depends on the initial concentration:
t1/2=2k[A]0 …