MCQMediumJEE 2025Integrated Rate Laws

JEE Chemistry 2025 Question with Solution

For the reaction AA \rightarrow products,

Graph of $$t_{1/2}$$ versus $$[A]_0$$ showing a straight line through the origin with slope approximately $$76.92$$ and a blank asking concentration of $$A$$ at $$10 \, \text{minutes}$$ in $$10^{-3} \, \text{mol L}^{-1}$$.

The reaction was started with 2.5mol L12.5 \, \text{mol L}^{-1} of AA.

  • A

    24352435

  • B

    20002000

  • C

    10001000

  • D

    30003000

Answer

Correct answer:A

Step-by-step solution

Standard Method

Given: The plot of t1/2t_{1/2} versus [A]0[A]_0 is a straight line through the origin with slope 76.9276.92. Initial concentration is [A]0=2.5mol L1[A]_0 = 2.5 \, \text{mol L}^{-1} and time is 10min10 \, \text{min}.

Find: The concentration of AA after 10min10 \, \text{min} in the form _____ \times 10^{-3} \, \text{mol L}^{-1}.

For a zero-order reaction,

t1/2=[A]02Kt_{1/2} = \frac{[A]_0}{2K}

So the slope of the graph is

slope=12K=76.92\text{slope} = \frac{1}{2K} = 76.92

Hence,

K=12×76.92=1153.84K = \frac{1}{2 \times 76.92} = \frac{1}{153.84}

Now use the zero-order integrated rate law,

[A]=[A]0Kt[A] = [A]_0 - Kt

Substituting the values,

[A]=2.51153.84×10[A] = 2.5 - \frac{1}{153.84} \times 10 [A]=2.435mol L1[A] = 2.435 \, \text{mol L}^{-1}

Therefore,

2.435mol L1=2435×103mol L12.435 \, \text{mol L}^{-1} = 2435 \times 10^{-3} \, \text{mol L}^{-1}

So, the correct option is A.

Using slope of half-life graph

Given: A graph of t1/2t_{1/2} versus [A]0[A]_0 is linear and passes through the origin. The slope is 76.9276.92. Also, [A]0=2.5mol L1[A]_0 = 2.5 \, \text{mol L}^{-1}.

Find: Concentration of AA after 10min10 \, \text{min}.

For a zero-order reaction, the half-life depends directly on initial concentration:

t1/2[A]0t_{1/2} \propto [A]_0

with formula

t1/2=[A]02kt_{1/2} = \frac{[A]_0}{2k}

Comparing with the straight-line form,

t1/2=(12k)[A]0t_{1/2} = \left(\frac{1}{2k}\right)[A]_0

therefore,

12k=76.92\frac{1}{2k} = 76.92

So,

k=1153.84mol L1min1k = \frac{1}{153.84} \, \text{mol L}^{-1} \text{min}^{-1}

Now apply the integrated rate law for zero-order kinetics:

[A]t=[A]0kt[A]_t = [A]_0 - kt

At t=10mint = 10 \, \text{min},

[A]10=2.510153.84[A]_{10} = 2.5 - \frac{10}{153.84} [A]102.50.06500[A]_{10} \approx 2.5 - 0.06500 [A]102.435mol L1[A]_{10} \approx 2.435 \, \text{mol L}^{-1}

Expressing this in the required form,

2.435mol L1=2435×103mol L12.435 \, \text{mol L}^{-1} = 2435 \times 10^{-3} \, \text{mol L}^{-1}

Therefore, the correct option is A, that is 24352435.

Common mistakes

  • Using the first-order half-life formula is incorrect because here the graph shows t1/2[A]0t_{1/2} \propto [A]_0, which is characteristic of a zero-order reaction. Use t1/2=[A]02kt_{1/2} = \frac{[A]_0}{2k} instead.

  • Taking the slope as kk directly is wrong. From the graph, the slope is 12k\frac{1}{2k}, not kk. First convert the slope into the rate constant before substituting into the integrated equation.

  • Writing [A]=[A]0+kt[A] = [A]_0 + kt is a sign error. In a zero-order reaction, concentration decreases with time, so the correct relation is [A]=[A]0kt[A] = [A]_0 - kt.

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