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JEE • CHEMISTRY • CHEMICAL KINETICS

Chemical kinetics practice · Medium

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Showing 1-30 of 144 questions
1 Medium
1 of 144
Understanding +4 | -1
Which of the following is a zero order reaction?
View answer and explanation
Correct option: A
2NH3(g)→Pt catalyst1130 KN2(g)+3H2(g)2{\text{N}}{{\text{H}}_3}\left( {\text{g}} \right)\xrightarrow[{{\text{Pt catalyst}}}]{{1130\,{\text{K}}}}{{\text{N}}_{\text{2}}}\left( {\text{g}} \right) + 3{{\text{H}}_{\text{2}}}\left( {\text{g}} \right) (Reactant NH3\mathrm{NH}_3 is strongly adsorbed
Option A (2NH3(g)→Pt catalyst1130 KNext2(g)+3Hext2(g)2{\text{N}}{{\text{H}}_3}\left( {\text{g}} \right)\xrightarrow[{{\text{Pt catalyst}}}]{{1130{\,\text{K}}}}{{\text{N}}_{ ext{2}}}\left( {\text{g}} \right) + 3{{\text{H}}_{ ext{2}}}\left( {\text{g}} \right) (Reactant NH3\mathrm{NH}_3 is strongly adsorbed) is correct because the decomposition of ammonia on a platinum surface at high pressure is a zero-order reaction due to the surface being saturated with ammonia.
2 Medium
2 of 144
Application +4 | -1
The energy of activation for an uncatalysed reaction is 100 kJ/mol.100 \mathrm{~kJ/mol}. Presence of a catalyst lowers the energy of activation by 75%75 \%. The log⁡10K2K1\log _{10} \frac{K_2}{K_1} of the ratio of rate constant of catalysed and uncatalysed reactions at 27∘C27^{\circ} \mathrm{C} is?

Assume the frequency factor is same for both reactions. (Given 2.303×8.314=19.1472.303 \times 8.314=19.147)
View answer and explanation
Correct option: A
13.05
Option A (13.05) is correct because it is the result of calculating the ratio of rate constants using the Arrhenius equation and the given activation energies.
3 Medium
3 of 144
Application +4 | -1
A first order reaction has a rate constant 1.15×10−3S−11.15 \times {10^{ - 3}}{S^{ - 1}}. How long will 5g of this reactant take to reduce to 3g (given log 1.667 = 0.2219)
View answer and explanation
Correct option: B
444 S
Option B (444 S) is correct because the time is calculated using the first-order kinetics equation with the given rate constant and initial/final amounts.
4 Medium
4 of 144
Application +4 | -1
For the reaction, A(g)→B(g)+C(g)\mathrm{A}(\mathrm{g}) \rightarrow \mathrm{B}(\mathrm{g})+\mathrm{C}(\mathrm{g}). The initial pressure was P0\mathrm{P}_0 while pressure after time ' t\mathrm{t} ' was Pt\mathrm{P}_{\mathrm{t}}. The rate constant k\mathrm{k} will be given by:
View answer and explanation
Correct option: C
k=2.303tlog⁡P02P0−Pt\mathrm{k}=\frac{2.303}{\mathrm{t}} \log \frac{\mathrm{P}_0}{2 \mathrm{P}_0-\mathrm{P}_{\mathrm{t}}}
Option C (k=2.303tlog⁡P02P0−Pt\mathrm{k}=\frac{2.303}{\mathrm{t}} \log \frac{\mathrm{P}_0}{2 \mathrm{P}_0-\mathrm{P}_{\mathrm{t}}}) is correct because it correctly applies the integrated rate law for a first-order gas-phase reaction.
5 Medium
5 of 144
Application +4 | -1
For the reaction 2N2O5→4NO2+O22 \mathrm{N}_2 \mathrm{O}_5 \rightarrow 4 \mathrm{NO}_2+\mathrm{O}_2 rate & rate constant are 1.02×10−41.02 \times 10^{-4} and 3.4×10−5sec−13.4 \times 10^{-5} \mathrm{sec}^{-1} respectively then concentration of N2O5\mathrm{N}_2 \mathrm{O}_5 at that time will be:
View answer and explanation
Correct option: B
3
Option B (3) is correct because the concentration of N2O5 is calculated directly from the rate law, given the rate and rate constant.
6 Medium
6 of 144
Application +4 | -1
The value of rate constant for the above reaction is:
View answer and explanation
Correct option: D
None of these
The correct answer is None of these because the rate constant cannot be determined without more information about the rate of reaction.
7 Medium
7 of 144
Analyzing +4 | -1
STATEMENT-1: Active complex is an intermediate product.

STATEMENT-2 : Active complex is unstable with high vibrational energy.
View answer and explanation
Correct option: D
If STATEMENT-1 is FALSE and STATEMENT-2 is TRUE
Option D is correct because Statement-1 is false, as the active complex is an intermediate product, and Statement-2 is true, as the active complex is unstable with high vibrational energy.
8 Medium
8 of 144
Analyzing +4 | -1
Statement I For the reaction

2KClO3⟶2KCl+3O2−d[KClO3]dt=23d[O2]dt\begin{aligned} & 2 \mathrm{KClO}_3 \longrightarrow 2 \mathrm{KCl}+3 \mathrm{O}_2 \\ & \frac{-d\left[\mathrm{KClO}_3\right]}{d t}=\frac{2}{3} \frac{d\left[\mathrm{O}_2\right]}{d t} \end{aligned}

Statement II If average rate of formation of O2\mathrm{O}_2 is 0.01 mol0.01 \mathrm{~mol} min−1\mathrm{min}^{-1}, rate of disappearance of KClO3\mathrm{KClO}_3 is 0.03 mol min−10.03 \mathrm{~mol} \mathrm{~min}^{-1}.
View answer and explanation
Correct option: C
Statement I is correct but Statement II is incorrect
The correct answer is C because Statement I is correct based on the stoichiometry of the reaction, but Statement II is incorrect as the rate of disappearance of KClO₃ should be 0.02 mol min⁻¹ when the rate of formation of O₂ is 0.03 mol min⁻¹.
9 Medium
9 of 144
Analyzing +4 | -1
For the reaction A+B→2C+D,A+B \rightarrow 2 C+D, which of the following statement are incorrect?
View answer and explanation
Correct option: A
Rate of disappearance of B=2×rate of appearance of C\text{Rate of disappearance of }B =2 \times \text{rate of appearance of }C
The correct answer is A (Rate of disappearance of B = 2 x rate of appearance of C) because, according to the stoichiometry of the reaction, the rate of disappearance of B should be half the rate of appearance of C.
10 Medium
10 of 144
Analyzing +4 | -1
Assertion: Acid catalyzed of ethyl acetate is a first order reaction.

Reason: Water does not take part in the reaction.
View answer and explanation
Correct option: C
If Assertion is True but the Reason is False
Option C (If Assertion is True but the Reason is False) is correct because the acid-catalyzed hydrolysis of ethyl acetate is pseudo-first order, but water does participate in the reaction.
11 Medium
11 of 144
Understanding +4 | -1
The order of a reaction with rate equal to k  CA3/2  CB−1/2k\;C_A^{3/2}\;C_B^{ - 1/2} is
View answer and explanation
Correct option: A
1
Option A (1) is correct because the order of the reaction is the sum of the exponents of the concentration terms in the rate law, which in this case is 3/2 + (-1/2) = 1.
12 Medium
12 of 144
Understanding +4 | -1
STATEMENT 1 : Product can form only when the required orientation and energy conditions are met
STATEMENT-2 : All collisions between reactants yield the desired product.
View answer and explanation
Correct option: C
If STATEMENT-1 is TRUE and STATEMENT-2 is FALSE
Option C (If STATEMENT-1 is TRUE and STATEMENT-2 is FALSE) is correct because product formation requires specific orientation and energy, but not all collisions lead to product formation.
13 Medium
13 of 144
Application +4 | -1
For a first order reaction rate constant is given as, log⁡  K=14−1.2×104T\log \,\,K = 14 - \frac{{1.2 \times {{10}^4}}}{T}, then what will be value of ′T′'T' if its half-life is 6.93×10−3  min⁡6.93 \times {10^{ - 3}}\,\,\min
View answer and explanation
Correct option: B
1000 K
Option B (1000 K) is correct because the temperature is calculated using the Arrhenius equation and the given half-life.
14 Medium
14 of 144
Application +4 | -1
If rate constant of a reaction is 2×10−4  s−12 \times 10^{-4} \,{~s}^{-1} then the time required for the completion of 90%90 \% of the reaction is
View answer and explanation
Correct option: A
1.15×104  s1.15 \times 10^4\, {~s}
Option A (1.15×104  s1.15 \times 10^4\, \mathrm{~s}) is correct because it is the time calculated using the first-order kinetics equation for 90% completion of the reaction.
15 Medium
15 of 144
Application +4 | -1
The first order rate constant for the decomposition of ethyl iodide by the reaction C2H5I(g)→C2H4(g)+HI(g){C_2}{H_5}I\left( g \right) \to {C_2}{H_4}\left( g \right) + HI\left( g \right) at 600 K is 1.60×10−5  s−1.1.60 \times {10^{ - 5}}\,\,{s^{ - 1}}. Its energy of activation is 209 kJ/mol, T the rate constant of the reaction at 700 K is.
View answer and explanation
Correct option: B
6.36×10−3  s−16.36 \times {10^{ - 3}}\,\,{s^{ - 1}}
Option B (6.36×10−3 s−16.36 \times {10^{ - 3}}\,{s^{ - 1}}) is correct because it is calculated using the Arrhenius equation relating rate constants at different temperatures.
16 Medium
16 of 144
Application +4 | -1
Half life of a first order reaction:

A(A( aq. )→2B(aq)) \rightarrow 2 B(a q) is 40 min at 27∘C27^{\circ} \mathrm{C} and 20 min at 37∘C37^{\circ} \mathrm{C}. The activation energy of reaction is (ln⁡2=0.7,R=2.0 cal mol−1K−1)\left(\ln 2=0.7, R=2.0 \mathrm{~cal} \mathrm{~mol}^{-1} K^{-1}\right)
View answer and explanation
Correct option: B
13020 cal/mol
Option B (13020 cal/mol) is correct because it is the calculated activation energy using the Arrhenius equation and the given half-lives at different temperatures.
17 Medium
17 of 144
Application +4 | -1
For the reaction 2N2O5(g)→4NO2(g)+O2(g),2 \mathrm{N}_2 \mathrm{O}_5(\mathrm{g}) \rightarrow 4 \mathrm{NO}_2(\mathrm{g})+\mathrm{O}_2(\mathrm{g}), the concentration of NO2\mathrm{NO}_2 increases by 2.4×10−2M2.4 \times 10^{-2} \mathrm{M} in 6 s.6 \mathrm{~s}. What will be the average rate of appearance of NO2\mathrm{NO}_2 and the average rate of disappearance of N2O5?\mathrm{N}_2 \mathrm{O}_5?
View answer and explanation
Correct option: D
4×10−3Ms−1,2×10−3Ms−14 \times 10^{-3} \mathrm{Ms}^{-1}, 2 \times 10^{-3} \mathrm{Ms}^{-1}
Option D (4×10−3Ms−1,2×10−3Ms−14 \times 10^{-3} \mathrm{Ms}^{-1}, 2 \times 10^{-3} \mathrm{Ms}^{-1}) is correct because the average rate of appearance of NO2 and disappearance of N2O5 are calculated based on the stoichiometry of the reaction.
18 Medium
18 of 144
Application +4 | -1
The half-life of first order decomposition of NH4NO3\mathrm{NH}_4 \mathrm{NO}_3 is 2.10hr2.10 \mathrm{hr} at 288 K288 \mathrm{~K} temperature NH4NO3(aq)⟶N2O(g)+2H2O(l)\mathrm{NH}_4 \mathrm{NO}_3(a q) \longrightarrow \mathrm{N}_2 \mathrm{O}(g)+2 \mathrm{H}_2 \mathrm{O}(l), if 6.2 g6.2 \mathrm{~g} of NH4NO3\mathrm{NH}_4 \mathrm{NO}_3 is allowed to decompose, The time required for NH4NO3\mathrm{NH}_4 \mathrm{NO}_3 to decompose 90%90 \% is :
View answer and explanation
Correct option: A
6.978 hr6.978 \mathrm{~hr}
Option A (6.978 hr6.978 \mathrm{~hr}) is correct because it accurately calculates the time required for 90% decomposition of NH4NO3\mathrm{NH}_4 \mathrm{NO}_3 using first-order kinetics.
19 Medium
19 of 144
Understanding +4 | -1
Statement I: The overall order of the reaction is the sum of the exponents of all the reactants in the rate expression

Statement II: There are many higher-order reactions
View answer and explanation
Correct option: B
If statement I and statement II are correct but statement II is not the correct explanation of statement I
Option B (If statement I and statement II are correct but statement II is not the correct explanation of statement I) is correct because both statements are true, but the existence of higher-order reactions does not explain the definition of overall order.
20 Medium
20 of 144
Understanding +4 | -1
Nuclear reaction accompanied with emission of neutron(s) is:
View answer and explanation
Correct option: A
1327Al+24He⟶1530P+01n{ }_{13}^{27} {Al}+{ }_2^4 {He} \longrightarrow{ }_{15}^{30} {P}+{ }_0^1 {n}
Option A (1327Al+24He⟶1530P+01n{ }_{13}^{27} {Al}+{ }_2^4 {He} \longrightarrow{ }_{15}^{30} {P}+{ }_0^1 {n}) is correct because it shows the emission of a neutron (01n{ }_0^1 {n}) as a product of the nuclear reaction.
21 Medium
21 of 144
Application +4 | -1
89Ac231{ }_{89} A c^{231} after emission of some α\alpha and β\beta-particles gives 82Pb207{ }_{82} P b^{207}. The number of such α\alpha and β−\beta-particles are respectively
View answer and explanation
Correct option: B
6, 5
Option B (6, 5) is correct because the number of alpha particles is calculated from the mass number difference, and beta particles from the atomic number difference.
22 Medium
22 of 144
Understanding +4 | -1
When a graph is plot for log⁡[A]\log [\mathrm{A}] against time (t), then the slope and intercept of the line for first order reaction is equal to
View answer and explanation
Correct option: C
−k2.303,log⁡[A]0\frac{-\mathrm{k}}{2.303}, \log [\mathrm{A}]_0
Option C (−k2.303,log⁡[A]0\frac{{-\mathrm{k}}}{{2.303}}, \log [\mathrm{A}]_0) is correct because it matches the slope and intercept derived from the integrated rate law for a first-order reaction when plotting log⁡[A]\log[A] vs. time.
23 Medium
23 of 144
Application +4 | -1
For a first order reaction, A⟶A \longrightarrow products, the initial concentration of A\mathrm{A} decrease from 0.1 M0.1 \mathrm{~M} to 0.05 M0.05 \mathrm{~M} in 1 minutes. The initial rate of the reaction (in Ms−1\mathrm{M} \mathrm{s}^{-1} ) is
View answer and explanation
Correct option: C
1.15×10−31.15 \times 10^{-3}
Option C (1.15×10−31.15 \times 10^{-3}) is correct because the rate of a first-order reaction is directly proportional to the concentration of the reactant, and the rate constant can be calculated from the half-life.
24 Medium
24 of 144
Analyzing +4 | -1
Assertion : The kinetics of the reaction

mA+nB+pC⟶m′X+n′Y+p′Zm A+n B+p C \longrightarrow m^{\prime} X+n^{\prime} Y+p^{\prime} Z

obey the rate expression as dXdt=k[A]m[B]n\frac{d X}{d t}=k[A]^m[B]^n.

Reason : The rate of the reaction does not depend upon the concentration of CC.
View answer and explanation
Correct option: A
If both Assertion and Reason are correct and the Reason is the correct explanation of Assertion.
Option A is correct because the rate expression given is consistent with the rate depending only on the concentrations of A and B.
25 Medium
25 of 144
Application +4 | -1
If the initial concentration of reactants are doubled half life becomes half. Then order of the reaction will be
View answer and explanation
Correct option: B
2
Option B (2) is correct because the half-life is inversely proportional to the initial concentration raised to the power of (n-1), where n is the order of the reaction.
26 Medium
26 of 144
Application +4 | -1
On doubling the concentration of reactant, if half-life also gets doubled then the order of reaction will be
View answer and explanation
Correct option: A
Zero
Option A (Zero) is correct because for a zero-order reaction, the half-life is directly proportional to the initial concentration of the reactant.
27 Medium
27 of 144
Analyzing +4 | -1
Two reactions A→productsA \to products and B→productsB \to products have rate constants KA{K_A} and KB{K_B} at temperature TT and activation energies EA{E_A} and EB{E_B} respectively. If KA>KB{K_A} > {K_B}&nbsp; and EA<EB{E_A} < {E_B} and assuming that AA for both the reactions is same, then:
View answer and explanation
Correct option: D
All of the above
Option D (All of the above) is correct because the given conditions satisfy the Arrhenius equation, and the relative magnitudes of rate constants change with temperature as described.
28 Medium
28 of 144
Understanding +4 | -1
Assertion (A): Molecularity of a reaction cannot be more than three.
Reason (R): Probability of simultaneous collision between more than three particles is very less.
View answer and explanation
Correct option: A
Both (A) and (R) are true (R) is the correct explanation of (A)
Option A is correct because both the assertion and the reason are true, and the reason correctly explains why molecularity cannot exceed three.
29 Medium
29 of 144
Understanding +4 | -1
The slope of the line obtained on plotting log⁡10k\log _{10} \mathrm{k} against 1T\frac{1}{\mathrm{T}} is equal to
View answer and explanation
Correct option: D
−Ea2.303R\frac{-\mathrm{E}_{\mathrm{a}}}{2.303 \mathrm{R}}
Option D is correct because, according to the Arrhenius equation, the slope of the plot of log10 k against 1/T is equal to -Ea/(2.303R).
30 Medium
30 of 144
Analyzing +4 | -1
The activation energies of two reactions are Ea{E_a} and Ea′{E'_a} with Ea>Ea′.{E_a} > {E'_a}. If the temperature of the reacting systems is increased from T1{T_1} to T2{T_2}, predict which alternative is correct. K′K' are rate constants at higher temperature. Assume AA being same for both the reactions:
View answer and explanation
Correct option: B
K1<K2{K_1} < {K_2} and K2′<K1′{K'_2} < {K'_1}
The correct answer is B (K1<K2{K_1} < {K_2} and K2′<K1′{K'_2} < {K'_1}) because a higher activation energy implies a smaller rate constant, and the effect of temperature is more pronounced for reactions with higher activation energies.
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