Q.Show that in a first order reaction, time required for completion of 99.9% is 10 times of half-life (t1/2) of the reaction.
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First Order Kinetics
Imagine you have a bucket of water with a small hole at the bottom. The water drains out. At the start, the bucket is full, so the pressure at the hole is high — water gushes out fast. As the water level drops, the pressure decreases, and the water trickles out more slowly. The rate at which water leaves is directly proportional to how much water is still in the bucket.
That's the core intuition behind first order kinetics: the rate of a process depends linearly on how much of the substance is left.
The Precise Statement
In chemistry, first order kinetics describes a reaction where the rate of the reaction is directly proportional to the concentration of one reactant.
If we have a reaction: A→products, then:
Rate=−dtd[A]=k[A]
Here:
- [A] is the concentration of reactant A at any time t
- k is the rate constant (units: time−1, e.g., s−1)
- The negative sign indicates that [A] decreases over time
The key point: double the concentration, double the rate. Halve the concentration, halve the rate.
The Integrated Form — What Actually Happens Over Time
The differential equation above tells us the instantaneous rate. But what we usually want is: how does concentration change with time?
Integrating gives:
ln[A]t=ln[A]0−kt
or equivalently:
[A]t=[A]0e−kt
Where [A]0 is the initial concentration and [A]t is the concentration at time t.
This exponential decay is the hallmark of first order kinetics. The concentration drops rapidly at first, then more slowly, approaching zero asymptotically.
The Half-Life — A Beautiful Constant
For first order kinetics, the half-life (t1/2) — the time taken for half the reactant to be consumed — is independent of the starting concentration.
t1/2=kln2≈k0.693
This is a powerful result. Whether you start with 100 g or 1 g, it always takes the same time to go from that amount to half of it. This is unique to first order kinetics — no other order has this property.
For a first order process, after n half-lives, the fraction remaining is (21)n. After 1 half-life: 50% remains. After 2: 25%. After 3: 12.5%. And so on.
How to Identify First Order Kinetics Experimentally
If you plot ln[A] versus time and get a straight line with slope −k, the reaction is first order. This is the gold standard test.
Alternatively, if the half-life remains constant as you change the initial concentration, that's a strong indicator.
Real-World Examples
- Radioactive decay: Every radioactive isotope decays by first order kinetics. Carbon-14 dating works because t1/2=5730 years, regardless of how much carbon-14 is present. …
Why this formula?
First Order Kinetics: Why the Formula Holds
Let's build this from the core idea — not just memorise the equation.
The Fundamental Assumption
In a first order reaction, the rate of reaction depends linearly on the concentration of only one reactant.
If we have:
A→products
The rate law is:
Rate=−dtd[A]=k[A]
Here:
- −dtd[A] = rate of disappearance of A (negative because [A] decreases)
- k = rate constant (units: time−1, e.g., s−1)
- [A] = concentration of A at any time
Why linear? Because the probability of a single molecule reacting in a given time is constant — it doesn't depend on other molecules. This is the molecular logic behind first order.
Deriving the Integrated Rate Law
We start from the differential form:
−dtd[A]=k[A]
Step 1: Separate variables
Bring all [A] terms to one side, dt to the other:
[A]d[A]=−kdt
Step 2: Integrate both sides
Integrate from initial time t=0 (concentration [A]0) to any time t (concentration [A]t):
∫[A]0[A]t[A]d[A]=−k∫0tdt
The left side integrates to ln[A]:
ln[A]t−ln[A]0=−kt
Step 3: Rearrange
ln[A]0[A]t=−kt
Or equivalently:
ln[A]t=ln[A]0−kt
This is the integrated rate law for first order kinetics.
Why This Form Makes Sense
- Exponential decay: Taking antilog:
[A]t=[A]0e−kt
The concentration decays exponentially — a hallmark of first order processes.
- Constant half-life: The time for [A]t to become half of [A]0 is:
2[A]0=[A]0e−kt1/2
21=e−kt1/2
ln(21)=−kt1/2
t1/2=kln2
Key insight: t1/2 is independent of initial concentration — unique to first order. This is why radioactive decay (a first order process) has a fixed half-life regardless of how much you start with.
Graphical Interpretation (Exam-Ready) …
Concept: First Order Kinetics — For a first order reaction, the integrated rate law is k=t2.303log[A][A]0.
Step 1: Half-life t1/2 is the time when [A]=2[A]0.
From the rate law:
t1/2=k2.303log[A]0/2[A]0=k2.303log2=k0.693.
Step 2: For 99.9% completion, [A]=0.1% of [A]0, i.e., [A]=1000[A]0. …
Using t=k2.303log[A][A]0: for 99.9% completion t=k6.909 and t1/2=k0.693. Their ratio is 0.6936.909≈10, so t99.9%≈10t1/2.
To show
For a first-order reaction the integrated rate law is
t=k2.303log[A][A]0
Half-life. At t1/2, [A]=2[A]0:
t1/2=k2.303log2=k2.303(0.3010)=k0.693
Time for 99.9% completion. When 99.9% has reacted, 0.1% remains, so [A]=1000[A]0:
t99.9%=k2.303log[A]0/1000[A]0=k2.303log1000=k2.303(3)=k6.909
Take the ratio. …
Method: Integrated Rate Law Approach for First-Order Kinetics
This method uses the integrated rate equation for a first-order reaction and compares the time for 99.9% completion with the half-life.
Steps
Step 1: Write the integrated rate law for first-order kinetics
For a first-order reaction:
k=t2.303log[A][A]0
Where:
- k = rate constant
- t = time
- [A]0 = initial concentration
- [A] = concentration at time t
Step 2: Express half-life (t1/2)
At half-life, [A]=2[A]0:
t1/2=k2.303log[A]0/2[A]0=k2.303log2
Since log2=0.3010:
t1/2=k0.693
Step 3: Find time for 99.9% completion (t99.9%)
99.9% completion means only 0.1% remains:
[A]=0.1% of [A]0=1000.1[A]0=1000[A]0
Substitute into the integrated rate law:
t99.9%=k2.303log[A]0/1000[A]0=k2.303log1000
Since log1000=3: …
Here are the common mistakes students make when proving that for a first-order reaction, t99.9%=10×t1/2, and how to avoid each.
Mistake 1: Using the wrong formula for t1/2
The error:
Students often write t1/2=k0.693 correctly, but then incorrectly use t99.9%=k2.303log0.1100 without checking the remaining fraction.
Why it’s wrong:
For 99.9% completion, the remaining reactant is 0.1%, not 0.1 of the original. The fraction remaining is 1000.1=0.001.
How to avoid:
Always write the integrated rate law as:
t=k2.303log[A]t[A]0
For 99.9% completion: [A]t=0.001[A]0, so:
t99.9%=k2.303log0.0011=k2.303log1000
Mistake 2: Incorrectly calculating log1000
The error:
Some students write log1000=3 but then forget to multiply by 2.303, or they use log10 and ln interchangeably without adjusting.
How to avoid:
Remember:
- log101000=3
- So t99.9%=k2.303×3=k6.909
Then compare with t1/2=k0.693:
t1/2t99.9%=0.693/k6.909/k=9.97≈10
Key check: Always compute the ratio numerically to confirm it’s exactly 10 (or very close).
Mistake 3: Assuming 99.9% means [A]t=0.1[A]0
The error:
Thinking “99.9% done” means only 0.1 of the reactant is left — but that’s 90% completion, not 99.9%.
How to avoid:
Use the percentage remaining formula:
Fraction remaining=1−100percentage completed
For 99.9% completed: fraction remaining =1−0.999=0.001
Mistake 4: Forgetting to state the final conclusion clearly
The error:
Students derive t99.9%=k6.909 and t1/2=k0.693, but don’t explicitly write:
t99.9%=10×t1/2
How to avoid:
Always end with a clear, boxed statement showing the relationship. In exams, this is often the mark-bearing line.
Mistake 5: Mixing up natural log and log base 10
The error:
Using ln instead of log10 in the formula t=k2.303log[A]t[A]0.
Why it’s wrong:
The integrated first-order rate law is:
t=k1ln[A]t[A]0 …
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