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Zero, First and Second Order Reactions

Zero, first, and second order reactions are classified by how rate depends on reactant concentration. Their integrated rate equations relate concentration and time, allowing calculation of rate constant, concentration remaining, or half-life.

In one line: Zero: [A] line; first: ln[A] line; second: 1/[A] line.

Practice This Concept

Understand it

  • In a zero order reaction, rate is independent of reactant concentration and [A] decreases linearly with time.
  • In a first order reaction, rate is proportional to [A], and ln[A] or log[A] gives a straight-line relation with time.
  • In a second order reaction involving one reactant, 1/[A] increases linearly with time.
  • Half-life behaviour is a strong identifier: zero order half-life depends directly on initial concentration, first order half-life is independent of initial concentration, and second order half-life is inversely proportional to initial concentration.

Example

For a first order decomposition with k = 2.31 × 10−3 s−1, t1/2 = 0.693/k = 0.693/(2.31 × 10−3) = 300 s. This means half the reactant remains after every 300 s interval.

Rule to remember

Zero order: [A] = [A0] - kt, t1/2 = [A0]/2k, k unit = mol L−1 s−1.

First order: ln[A] = ln[A0] - kt; k = (2.303/t)log([A0]/[A]); t1/2 = 0.693/k; k unit = s−1.

Second order: 1/[A] - 1/[A0] = kt; t1/2 = 1/(k[A0]); k unit = L mol−1 s−1.

See it worked out

Follow the example line by line, then use the same method on new questions.

Worked example

A first order reaction has [A0] = 0.80 mol L−1 and [A] = 0.20 mol L−1 after 40 min.

  1. 1k = (2.303/40)log(0.80/0.20) = (2.303/40)log4 = (2.303/40)(0.6021) = 0.0347 min−1.
  2. 2Interpretation: concentration becomes one-fourth in 40 min.

Method you can reuse

  1. 1Check the given clue: rate law, graph, half-life, or concentration-time data.
  2. 2Select the matching integrated equation.
  3. 3Keep time units consistent with k.
  4. 4Substitute values carefully, then state what the result means chemically, such as reactant left or fraction decomposed.

Visual tip

Graph comparison is important: [A] vs t is linear for zero order, ln[A] vs t is linear for first order, and 1/[A] vs t is linear for second order.

Check yourself

Answer the question in your head before opening the answer.

Try it yourself

Which graph is linear for a first order reaction: [A] vs t, ln[A] vs t, or 1/[A] vs t?

Think first, then show answer
ln[A] vs t is linear for a first order reaction, with slope = -k.

Common wrong answer

Using log formula without the factor 2.303, or mixing seconds and minutes when calculating k.

Don't mix this up

Students often use t1/2 = 0.693/k for every order, but that formula applies only to first order reactions.

Exam tip

Identify the order before choosing the equation. Graph clues are often faster than direct calculation.

Write it in the exam

Each point is worth about one mark. Write point 1 for a 1-mark question and keep adding points as the marks go up.

How CBSE asks it

This concept appears as numerical problems on k, t1/2, concentration left, and graph-based identification of order. Long-answer questions may ask for derivation or comparison of equations and half-life relations.
  1. 1

    Enough for 1 mark

    Zero, first, and second order reactions are classified by how rate depends on reactant concentration. Their integrated rate equations relate concentration and time, allowing calculation of rate constant, concentration remaining, or half-life.

  2. 2

    Add for 2 marks

    Example: For a first order decomposition with k = 2.31 × 10−3 s−1, t1/2 = 0.693/k = 0.693/(2.31 × 10−3) = 300 s. This means half the reactant remains after every 300 s interval.

  3. 3

    Add for 3 marks

    In a zero order reaction, rate is independent of reactant concentration and [A] decreases linearly with time.

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