Chemical Kinetics and Nuclear Chemistry — JEE Main practice

53 questions

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Sample questions with solutions

Q1 · 2026

Decomposition of A is a first order reaction at T(K) and is given by A(g) → B(g) + C(g).

In a closed 1 L vessel, 1 bar A(g) is allowed to decompose at T(K). After 100 minutes, the total pressure was 1.5 bar. What is the rate constant (in min1^{-1}) of the reaction? (log 2 = 0.3)

  • A.

    6.9×1046.9\times 10^{-4}

  • B.

    6.9×1016.9\times 10^{-1}

  • C.

    6.9×1026.9\times 10^{-2}

  • D.

    6.9×1036.9\times 10^{-3}

Answer: D
  1. Set up the pressure relationships. Given A decomposes to B and C in equal proportions, if xx bar of A decomposes,
Ptotal=(1x)+x+x=1+xP_{total} = (1-x)+x+x = 1+x
  1. Solve for x using the given total pressure. Given after 100 min, Ptotal=1.5P_{total}=1.5 bar,
1+x=1.5x=0.51+x=1.5 \quad \Rightarrow \quad x=0.5
  1. Find the remaining pressure of A. Given
PA=1x=0.5 barP_A = 1-x = 0.5\ \mathrm{bar}
  1. Apply the first-order rate law using pressure as a proxy for concentration. Given
k=2.303tlog(PA,0PA,t)=2.303100log(10.5)=2.303100×0.3=6.9×103 min1k = \frac{2.303}{t}\log\left(\frac{P_{A,0}}{P_{A,t}}\right) = \frac{2.303}{100}\log\left(\frac{1}{0.5}\right) = \frac{2.303}{100}\times 0.3 = 6.9\times 10^{-3}\ \mathrm{min}^{-1}

Hence, the answer is option D.

Q2 · 2026

A\mathrm{A}\rightarrow product (First order reaction).

Three sets of experiment were performed for a reaction under similar experimental conditions:

Run 1 ⇒ 100 mL of 10 M solution of reactant A

Run 2 ⇒ 200 mL of 10 M solution of reactant A

Run 3 ⇒ 100 mL of 10 M solution of reactant A + 100 mL of H2O\mathrm{H}_2\mathrm{O} added.

The correct variation of rate of reaction is

  • A.

    Run 1 = Run 2 = Run 3

  • B.

    Run 3 < Run 1 < Run 2

  • C.

    Run 1 < Run 2 < Run 3

  • D.

    Run 3 < Run 1 = Run 2

Answer: D
  1. Recall that first-order rate depends only on concentration, not volume. Since Rate =k[A]=k[A],

  2. Determine [A] in each run. Given Run 1 and Run 2 both use 10 M solution (just different volumes, concentration unchanged), while Run 3 is diluted with equal volume of water,

[A]Run3=10×100100+100=5 M[A]_{Run 3} = \frac{10\times 100}{100+100} = 5\ \mathrm{M}
  1. Compare the rates. Given
Rate1=k(10),Rate2=k(10),Rate3=k(5)\text{Rate}_1 = k(10),\quad \text{Rate}_2 = k(10),\quad \text{Rate}_3 = k(5)

so Run 1 = Run 2 > Run 3.

Hence, the answer is option D.

Q3 · 2026

Correct statements regarding Arrhenius equation among the following are:

A. Factor eEa/RTe^{-E_a/RT} corresponds to fraction of molecules having kinetic energy less than Ea.

B. At a given temperature, lower the Ea, faster is the reaction.

C. Increase in temperature by about 10C10^{\circ}\mathrm{C} doubles the rate of reaction.

D. Plot of logk\log k vs 1T\frac{1}{T} gives a straight line with slope =EaR=-\frac{E_a}{R}.

Choose the correct answer from the options given below:

  • A.

    B and C Only

  • B.

    A and B Only

  • C.

    B and D Only

  • D.

    A and C Only

Answer: A
  1. Check statement A. Since eEa/RTe^{-E_a/RT} actually represents the fraction of molecules with energy equal to or greater than EaE_a (able to overcome the barrier), not less than, statement A is incorrect.

  2. Check statement B. Given k=AeEa/RTk = Ae^{-E_a/RT}, a smaller EaE_a gives a larger eEa/RTe^{-E_a/RT} and thus a larger kk (faster reaction). Statement B is correct.

  3. Check statement C. Given this is a well-known empirical rule (rate roughly doubles for every 10°C rise for many reactions), statement C is correct.

  4. Check statement D. Since for base-10 logarithm,

logk=logAEa2.303R(1T)\log k = \log A - \frac{E_a}{2.303R}\left(\frac{1}{T}\right)

the slope is Ea2.303R-\frac{E_a}{2.303R}, not EaR-\frac{E_a}{R} (that slope applies to lnk\ln k vs 1/T1/T). Statement D is incorrect.

Hence, the correct statements are B and C only — the answer is option A.

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