Rate of reaction
Rate = -Δ[reactant]/Δt = +Δ[product]/Δt. Average rate over interval; instantaneous = -d[R]/dt at instant. Units: mol·L⁻¹·s⁻¹.
-- NCERT Class 12 Chemistry, Ch. 3, p. 4A common confusion that costs marks: treating the rate of a reaction as a single fixed number. The rate of a chemical reaction changes with time as reactants are consumed — what NEET tests is whether you understand how rate is defined and what the sign conventions mean.
What is rate of reaction? The rate of a chemical reaction is the change in concentration of a reactant or product per unit time (NCERT Class 12 Chemistry Chapter 3, page 4). For a general reaction aA + bB → cC + dD, the rate is expressed as:
Rate = −(1/a)(Δ[A]/Δt) = −(1/b)(Δ[B]/Δt) = +(1/c)(Δ[C]/Δt) = +(1/d)(Δ[D]/Δt)
The negative sign for reactants accounts for decreasing concentration; the positive sign for products accounts for increasing concentration. The stoichiometric coefficients (1/a, 1/b, etc.) normalise the rate so it is the same regardless of which species you measure.
Average vs. instantaneous rate. Average rate is Δ[concentration]/Δt over a finite interval. Instantaneous rate is the tangent slope (d[concentration]/dt) at a specific moment. NEET questions may give a concentration-time table and ask for the average rate over an interval, or they may ask you to distinguish the two.
The trap that bleeds marks: writing the rate expression without the stoichiometric coefficient. If 2NO₂ → 2NO + O₂, the rate of disappearance of NO₂ is −Δ[NO₂]/Δt, but the rate of reaction is −(1/2)(Δ[NO₂]/Δt). Forgetting the 1/2 gives an answer that is off by a factor of 2 — a distractor NTA loves to plant.
Watch-out: Units of rate are always mol L⁻¹ s⁻¹ (or mol L⁻¹ time⁻¹). If a question gives pressure changes for gaseous reactions, the unit shifts to atm s⁻¹, but the structure of the expression stays the same.
Select an option to see the explanation. Wrong answers show why your choice was tempting — and name the exact trap it exploits.
The rate of a chemical reaction is defined as:
For the reaction N₂ + 3H₂ → 2NH₃, the rate of reaction in terms of disappearance of H₂ is:
The SI unit of rate of a chemical reaction is:
For 2SO₂(g) + O₂(g) → 2SO₃(g), if the rate of formation of SO₃ is 4.0 × 10⁻² mol L⁻¹ s⁻¹, the rate of disappearance of O₂ is:
For the reaction A → 2B, if [A] decreases from 0.50 mol L⁻¹ to 0.40 mol L⁻¹ in 10 s, the average rate of formation of B is:
The concentration of a reactant drops from 0.80 mol L⁻¹ to 0.60 mol L⁻¹ in the first 20 s, and from 0.60 mol L⁻¹ to 0.45 mol L⁻¹ in the next 20 s. Which statement is correct?
For a gaseous reaction A(g) → B(g) + C(g), the rate of reaction can be expressed in terms of pressure change. If the total pressure increases at a rate of dp/dt, what is the rate of disappearance of A in terms of dp/dt?
For the reaction 2N₂O₅(g) → 4NO₂(g) + O₂(g), at a certain moment the rate of disappearance of N₂O₅ is 1.2 × 10⁻² mol L⁻¹ s⁻¹. The rate of formation of NO₂ and the rate of reaction are, respectively:
Given
- Reaction: 5Br⁻ + BrO₃⁻ + 6H⁺ → 3Br₂ + 3H₂O - Rate of disappearance of Br⁻ = 5.0 × 10⁻³ mol L⁻¹ s⁻¹
Required
(a) Rate of reaction (b) Rate of formation of Br₂
Concept
The rate of reaction is related to the rate of change of any species by dividing by the stoichiometric coefficient (with a negative sign for reactants): Rate = −(1/coefficient)(Δ[species]/Δt) for reactants, and +(1/coefficient)(Δ[species]/Δt) for products.
Formula
Rate of reaction = (1/5) × rate of disappearance of Br⁻ Rate of formation of Br₂ = 3 × rate of reaction
Substitution
Rate of reaction = (1/5) × 5.0 × 10⁻³ Rate of formation of Br₂ = 3 × rate of reaction
Calculation
Rate of reaction = (1/5)(5.0 × 10⁻³) = 1.0 × 10⁻³ mol L⁻¹ s⁻¹ Rate of formation of Br₂ = 3 × 1.0 × 10⁻³ = 3.0 × 10⁻³ mol L⁻¹ s⁻¹ Note: The stoichiometric coefficients (5, 3) are exact integers and do not affect significant figures. The answer retains 2 significant figures, matching the given data.
Final answer
(a) Rate of reaction = 1.0 × 10⁻³ mol L⁻¹ s⁻¹ (b) Rate of formation of Br₂ = 3.0 × 10⁻³ mol L⁻¹ s⁻¹
Common trap
A frequent error is skipping the stoichiometric coefficient and writing rate of reaction = 5.0 × 10⁻³ mol L⁻¹ s⁻¹ (equating it directly to the disappearance rate of Br⁻). This gives a value 5 times too large and leads to an incorrect Br₂ formation rate of 1.5 × 10⁻² mol L⁻¹ s⁻¹.
Similar NEET-style question
For 4NH₃(g) + 5O₂(g) → 4NO(g) + 6H₂O(g), if the rate of formation of NO is 2.0 × 10⁻⁴ mol L⁻¹ s⁻¹, calculate the rate of disappearance of O₂. [Answer: Rate of reaction = (1/4)(2.0 × 10⁻⁴) = 5.0 × 10⁻⁵ mol L⁻¹ s⁻¹. Rate of disappearance of O₂ = 5 × 5.0 × 10⁻⁵ = 2.5 × 10⁻⁴ mol L⁻¹ s⁻¹.] ---
Rate = -Δ[reactant]/Δt = +Δ[product]/Δt. Average rate over interval; instantaneous = -d[R]/dt at instant. Units: mol·L⁻¹·s⁻¹.
-- NCERT Class 12 Chemistry, Ch. 3, p. 4Temperature dependence of rate constant. Higher Ea → more T-sensitive rate.
| Symbol | Quantity | SI Unit |
|---|---|---|
| A | frequency factor | same as k |
| Ea | activation energy | J/mol |
| R | gas constant | J/mol/K |
| T | temp | K |
Compare rate constants at two temperatures to find Ea.
| Symbol | Quantity | SI Unit |
|---|---|---|
| k1, k2 | rate constants | same units |
| T1, T2 | temperatures | K |
| Ea | activation energy | J/mol |
Concentration decays exponentially. Half-life independent of [A]_0.
| Symbol | Quantity | SI Unit |
|---|---|---|
| [A] | conc at time t | mol/L |
| k | rate constant | 1/s |
| t | time | s |
Concentration decays linearly. Half-life depends on initial concentration.
| Symbol | Quantity | SI Unit |
|---|---|---|
| [A]_0 | initial conc | mol/L |
| k | rate constant | mol/L/s |
| t | time | s |
These are the exact patterns that cause wrong answers in NEET. Each trap includes when it triggers and how to avoid it.
Category: Similar Terms
Zero-order t_1/2 depends on [A]_0. First-order t_1/2 INDEPENDENT of [A]_0. Student uses wrong formula.
Half-life question with order specified.
1st order: t_1/2 = 0.693/k (constant). Zero order: t_1/2 = [A]_0/(2k) (varies with initial conc). Second order: t_1/2 = 1/(k[A]_0).
Root cause: sign error
ln(k2/k1) = (Ea/R) × (1/T1 - 1/T2). At higher T2, k2 > k1, so ln(k2/k1) > 0. Need 1/T1 > 1/T2.
Root cause: formula misuse
First order: t_1/2 = 0.693/k (constant). Zero order: t_1/2 = [A]_0/(2k) (depends on [A]_0). Second order: t_1/2 = 1/(k[A]_0).
Root cause: formula misuse
Zero-order: t_1/2 = [A]_0/(2k) (depends on initial conc). First-order: t_1/2 = 0.693/k (independent of [A]_0).
Root cause: concept gap
Rate law from EXPERIMENT, not stoichiometry. Order = sum of exponents in rate = k[A]^x[B]^y. Molecularity follows mechanism.
10 questions from NEET 2021, 2022, 2023, 2024, 2025. Answers verified against NTA official keys.
Activation energy of any chemical reaction can be calculated if one knows the value of
Which reaction is NOT a redox reaction?
Which one is an example of heterogenous catalysis?
Recurring question shapes from past papers. Each pattern shows why wrong options look tempting.
wrong sign of 1 over t
Mixes T1 and T2 in subtraction
uses zero order formula
Plugs into [A]_0/(2k) wrong-order formula
Test yourself on this topic with real past-paper questions:
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