MCQEasyJEE 2026Rate of Reaction

JEE Chemistry 2026 Question with Solution

Observe the following reactions at T(K)T(\text{K}). I. AproductsA \to \text{products}. II. 5Br+BrO3+6H+3Br2+3H2O5Br^- + BrO_3^- + 6H^+ \to 3Br_2 + 3H_2O. Both the reactions are started at 10.00am10.00 \, \text{am}. The rates of these reactions at 10.10am10.10 \, \text{am} are same. The value of d[Br]dt-\frac{d[Br^-]}{dt} at 10.10am10.10 \, \text{am} is 2×104mol L1min12 \times 10^{-4} \, \text{mol L}^{-1} \, \text{min}^{-1}. The concentration of AA at 10.10am10.10 \, \text{am} is 102mol L110^{-2} \, \text{mol L}^{-1}. What is the first order rate constant (in min1\text{min}^{-1}) of reaction I?

  • A

    2×1032 \times 10^{-3}

  • B

    4×1034 \times 10^{-3}

  • C

    10210^{-2}

  • D

    10310^{-3}

Answer

Correct answer:B

Step-by-step solution

Standard Method

Given: Reaction I is first order, so its rate is RI=k[A]R_I = k[A]. For reaction II, d[Br]dt=2×104mol L1min1-\frac{d[Br^-]}{dt} = 2 \times 10^{-4} \, \text{mol L}^{-1} \, \text{min}^{-1} at 10.10am10.10 \, \text{am}. Also, the rates of reactions I and II are equal at that time, and [A]=102mol L1[A] = 10^{-2} \, \text{mol L}^{-1}.

Find: The first order rate constant kk of reaction I.

For reaction II,

RII=15d[Br]dtR_{II} = -\frac{1}{5} \frac{d[Br^-]}{dt}

Substituting the given value,

RII=15(2×104)=4×105R_{II} = \frac{1}{5} \left(2 \times 10^{-4}\right) = 4 \times 10^{-5}

Since the rates are same at 10.10am10.10 \, \text{am},

RI=RII=4×105R_I = R_{II} = 4 \times 10^{-5}

For the first order reaction I,

RI=k[A]R_I = k[A]

So,

k(102)=4×105k \left(10^{-2}\right) = 4 \times 10^{-5}

Therefore,

k=4×103min1k = 4 \times 10^{-3} \, \text{min}^{-1}

Hence, the correct option is B.

Using Stoichiometric Rate Definition

Given: In reaction II, the stoichiometric coefficient of BrBr^- is 55. The disappearance rate of BrBr^- is given. The rates of reactions I and II are equal at 10.10am10.10 \, \text{am}.

Find: The value of kk for reaction I.

The rate of a reaction is obtained by dividing the rate of disappearance of a reactant by its stoichiometric coefficient. Therefore, for reaction II,

RII=15d[Br]dtR_{II} = -\frac{1}{5} \frac{d[Br^-]}{dt}

Using the given data,

RII=15(2×104)=4×105mol L1min1R_{II} = -\frac{1}{5} \left(-2 \times 10^{-4}\right) = 4 \times 10^{-5} \, \text{mol L}^{-1} \, \text{min}^{-1}

Now the question states that

RI=RIIR_I = R_{II}

Hence,

RI=4×105mol L1min1R_I = 4 \times 10^{-5} \, \text{mol L}^{-1} \, \text{min}^{-1}

For a first order reaction,

RI=k[A]R_I = k[A]

With [A]=102mol L1[A] = 10^{-2} \, \text{mol L}^{-1},

k×102=4×105k \times 10^{-2} = 4 \times 10^{-5}

Dividing both sides by 10210^{-2},

k=4×105102=4×103min1k = \frac{4 \times 10^{-5}}{10^{-2}} = 4 \times 10^{-3} \, \text{min}^{-1}

Therefore, the first order rate constant is 4×103min14 \times 10^{-3} \, \text{min}^{-1}.

Common mistakes

  • Using d[Br]dt-\frac{d[Br^-]}{dt} directly as the reaction rate for reaction II. This is wrong because the stoichiometric coefficient of BrBr^- is 55. Divide by 55 to get the actual rate of reaction: RII=15d[Br]dtR_{II} = -\frac{1}{5}\frac{d[Br^-]}{dt}.

  • Forgetting that reaction I is first order and writing RI=k[A]nR_I = k[A]^n with an arbitrary power. This is wrong because the question explicitly asks for the first order rate constant. Use RI=k[A]R_I = k[A].

  • Making an exponent error while dividing 4×1054 \times 10^{-5} by 10210^{-2}. This is wrong because dividing by 10210^{-2} increases the power of ten by 22. So 4×105102=4×103\frac{4 \times 10^{-5}}{10^{-2}} = 4 \times 10^{-3}, not 4×1074 \times 10^{-7} or 4×1024 \times 10^{-2}.

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