For a given reaction mathrmRrightarrow mathrmP,mathrmt_1 / 2$\mathrm{R}\rightarrow \mathrm{P},\mathrm{t}_{1 / 2}$ is related to [mathrmA]_0$[\mathrm{A}]_0$ as given in table :
Given: log 2 = 0.30$\log 2 = 0.30$
Which of the following is true?
A. The order of the reaction is frac12$\frac{1}{2}$ .
B. If [mathrmA]_0$[\mathrm{A}]_0$ is 1mathrmM$1\mathrm{M}$ , then mathrmt_1/2$\mathrm{t}_{1/2}$ is 200sqrt10$200\sqrt{10}$ min
C. The order of the reaction changes to 1 if the concentration of reactant changes from 0.100 mathrmM$0.100 \mathrm{M}$ to 0.500 mathrmM$0.500 \mathrm{M}$ .
D. t_1 / 2$t_{1 / 2}$ is 800 mathrm~min$800 \mathrm{~min}$ for [mathrmA]_0 = 1.6 mathrmM$[\mathrm{A}]_0 = 1.6 \mathrm{M}$
Choose the correct answer from the options given below:
A.textA and C only$\text{A and C only}$
B.textA and B only$\text{A and B only}$
C.textA, B and D only$\text{A, B and D only}$
D.textC and D only$\text{C and D only}$
Solution & Explanation
### Related Formula
The dependence of half-life on initial concentration is given by:
t_1/2 propto frac1[A]_0^n-1$$t_{1/2} \propto \frac{1}{[A]_0^{n-1}}$$
### Step 1: Finding the reaction order (n)
Using the values provided:
frac(t_1/2)_1(t_1/2)_2 = left( frac[A]_0,2[A]_0,1 right)^n-1$$\frac{(t_{1/2})_1}{(t_{1/2})_2} = \left( \frac{[A]_{0,2}}{[A]_{0,1}} \right)^{n-1}$$frac200100 = left( frac0.0250.100 right)^n-1 Rightarrow 2 = left( frac14 right)^n-1$$\frac{200}{100} = \left( \frac{0.025}{0.100} \right)^{n-1} \Rightarrow 2 = \left( \frac{1}{4} \right)^{n-1}$$2 = 2^-2(n-1) Rightarrow 1 = -2n + 2 Rightarrow n = frac12$$2 = 2^{-2(n-1)} \Rightarrow 1 = -2n + 2 \Rightarrow n = \frac{1}{2}$$
Hence, statement A is correct.
### Step 2: Checking half-life at other concentrations
Since n = frac12$n = \frac{1}{2}$, t_1/2 propto sqrt[A]_0$t_{1/2} \propto \sqrt{[A]_0}$.
- For [A]_0 = 1\,mathrmM$[A]_0 = 1\,\mathrm{M}$:
frac200t_1/2 = sqrtfrac0.11 Rightarrow t_1/2 = 200sqrt10\,mathrmmin$$\frac{200}{t_{1/2}} = \sqrt{\frac{0.1}{1}} \Rightarrow t_{1/2} = 200\sqrt{10}\,\mathrm{min}$$
Hence, statement B is correct.
- For [A]_0 = 1.6\,mathrmM$[A]_0 = 1.6\,\mathrm{M}$:
frac200t_1/2 = sqrtfrac0.11.6 = sqrtfrac116 = frac14 Rightarrow t_1/2 = 800\,mathrmmin$$\frac{200}{t_{1/2}} = \sqrt{\frac{0.1}{1.6}} = \sqrt{\frac{1}{16}} = \frac{1}{4} \Rightarrow t_{1/2} = 800\,\mathrm{min}$$
Hence, statement D is correct.
### Pattern Recognition
Sees: Half-life reducing as initial concentration decreases.
Trap: Assuming all reactions are first or zero order without calculations.
Shortcut: Reduction of [A]_0$[A]_0$ by 4 causes reduction of t_1/2$t_{1/2}$ by 2 rightarrow$\rightarrow$ indicates a square root dependence (t_1/2 propto sqrtA_0$t_{1/2} \propto \sqrt{A_0}$), which implies n = 0.5$n = 0.5$.
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 12 Chemistry: Chemical Kinetics
Keywords:#half life is related to concentration as given in table#JEE Main 2025 Morning Q32#Chemical Kinetics JEE Main 2025#Order of Reaction JEE Main 2025
More Chemical Kinetics Previous-Year Questions — Page 3
Q30jee_main_2025_03_april_morningFirst Order Kinetics
In a reaction A+B
ightarrow C$A+B
ightarrow C$, initial concentrations of A and B are related as [A]_0=8[B]_0$[A]_{0}=8[B]_{0}$. The half lives of A and B are 10 min and 40 min. respectively. If they start to disappear at the same time, both following first order kinetics, after how much time will the concentration of both the reactants be same?
A. 60 min
B. 80 min
C. 20 min
D. 40 min
Solution
### Related Formula
For a first-order integrated rate law expression:
[A]_t = [A]_0 e^-k_A t quad textwhere k = fracln 2t_1/2$$[A]_t = [A]_0 e^{-k_A t} quad \text{where } k = \frac{ln 2}{t_{1/2}}$$
### Core Logic
We require the instantaneous concentration to be identical at time t$t$:
[A]_t = [B]_t implies [A]_0 e^-k_A t = [B]_0 e^-k_B t$$[A]_t = [B]_t implies [A]_0 e^{-k_A t} = [B]_0 e^{-k_B t}$$frac[A]_0[B]_0 = e^(k_A - k_B)t$$\frac{[A]_0}{[B]_0} = e^{(k_A - k_B)t}$$
### Step 1: Substituting Parameters
Substitute [A]_0 = 8[B]_0$[A]_0 = 8[B]_0$ and express rate constants in terms of half-lives:
8 = e^(k_A - k_B)t implies ln 8 = (k_A - k_B)t$$8 = e^{(k_A - k_B)t} implies ln 8 = (k_A - k_B)t$$3ln 2 = ln 2 left( frac1(t_1/2)_A - frac1(t_1/2)_B
ight) times t$$3ln 2 = ln 2 \left( \frac{1}{(t_{1/2})_A} - \frac{1}{(t_{1/2})_B}
ight) \times t$$3 = left( frac110 - frac140
ight) times t implies 3 = frac340 times t implies t = 40text min.$$3 = \left( \frac{1}{10} - \frac{1}{40}
ight) \times t implies 3 = \frac{3}{40} \times t implies t = 40\text{ min.}$$
### Pattern Recognition
Shortcut: Express the concentration drop using half-life indices:
[A]_t = frac[A]_02^t/10 = frac8[B]_02^t/10$$[A]_t = \frac{[A]_0}{2^{t/10}} = \frac{8[B]_0}{2^{t/10}}$$[B]_t = frac[B]_02^t/40$$[B]_t = \frac{[B]_0}{2^{t/40}}$$
Equating both: 8 cdot 2^-t/10 = 2^-t/40 implies 2^3 = 2^fract10 - fract40 implies 3 = frac3t40 implies t = 40text min.$8 \cdot 2^{-t/10} = 2^{-t/40} implies 2^3 = 2^{\frac{t}{10} - \frac{t}{40}} implies 3 = \frac{3t}{40} implies t = 40\text{ min.}$
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 12 Chemistry: Chemical Kinetics
Q40jee_main_2025_04_april_eveningArrhenius Equation and Activation Energy
Consider the following plots of log of rate constant k (log k) vs frac1mathrmT$\frac{1}{\mathrm{T}}$ for three different reactions. The correct order of activation energies of these reactions is
The graph depicts three linear curves with distinct negative slopes showing the temperature dependence of rate constants.
### Related Formula
log k = log A - fracE_a2.303 R T$$\log k = \log A - \frac{E_a}{2.303 R T}$$textSlope of the line = -fracE_a2.303 R implies |textSlope| propto E_a$$\text{Slope of the line} = -\frac{E_a}{2.303 R} \implies |\text{Slope}| \propto E_a$$
### Core Logic
From the given graph, we look at the steepness (magnitude of the negative slope) of lines 1, 2, and 3:
- Line 2 is the steepest, meaning it has the largest slope magnitude.
- Line 1 has an intermediate slope.
- Line 3 is the flattest, indicating the smallest slope magnitude.
Since the activation energy E_a$E_a$ is directly proportional to the magnitude of this slope:
|textSlope_2| > |textSlope_1| > |textSlope_3| implies E_a2 > E_a1 > E_a3$$|\text{Slope}_2| > |\text{Slope}_1| > |\text{Slope}_3| \implies E_{a2} > E_{a1} > E_{a3}$$
### Pattern Recognition
In Arrhenius coordinates, steepness equals barriers. A steeper line means the reaction rate is highly sensitive to temperature because it has a higher activation energy (E_a$E_a$).
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 12 Chemistry: Chemical Kinetics
Half-life of zero order reaction mathrmA rightarrow$\mathrm{A} \rightarrow$ product is 1 hour, when initial concentration of reaction is 2.0 mathrm~mol mathrmL^-1$2.0 \mathrm{~mol} \mathrm{L}^{-1}$ . The time required to decrease concentration of A from 0.50 to 0.25 mathrm~mol mathrmL^-1$0.25 \mathrm{~mol} \mathrm{L}^{-1}$ is:
A. 0.5 hour
B. 4 hour
C. 15 min
D. 60 min
Solution
### Related Formula
t_1/2 = frac[A]_02k quad text(for Zero-Order रिएक्शन)$$t_{1/2} = \frac{[A]_0}{2k} \quad \text{(for Zero-Order रिएक्शन)}$$t = frac[A]_0 - [A]_tk$$t = \frac{[A]_0 - [A]_t}{k}$$
### Core Logic
1. Find the rate constant k$k$ using the given half-life parameters:
1 text hour = 60 text min = frac2.02k implies k = frac2.02 times 60 = frac160 mathrm~M cdot min^-1$$1 \text{ hour} = 60 \text{ min} = \frac{2.0}{2k} \implies k = \frac{2.0}{2 \times 60} = \frac{1}{60} \mathrm{~M \cdot min^{-1}}$$
2. Calculate the time t$t$ to drop from 0.50 mathrm~molcdot L^-1$0.50 \mathrm{~mol\cdot L^{-1}}$ to 0.25 mathrm~molcdot L^-1$0.25 \mathrm{~mol\cdot L^{-1}}$:
t = frac0.50 - 0.25k = frac0.25left(frac160right) = 0.25 times 60 = 15 text minutes$$t = \frac{0.50 - 0.25}{k} = \frac{0.25}{\left(\frac{1}{60}\right)} = 0.25 \times 60 = 15 \text{ minutes}$$
### Pattern Recognition
For zero-order systems, the rate of reaction is entirely independent of concentration. This means the time required to consume a specific quantity of reactant scales linearly with the concentration change (t = fracDelta Ck$t = \frac{\Delta C}{k}$).
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 12 Chemistry: Chemical Kinetics
Q32jee_main_2025_04_april_morningEffect of Catalyst
For A_2 + B_2 rightleftharpoons 2AB$A_2 + B_2 \rightleftharpoons 2AB$, E_a$E_a$ for forward and backward reaction are 180$180$ and 200mathrm~kJ~mol^-1$200\mathrm{~kJ~mol}^{-1}$ respectively. If catalyst lowers E_a$E_a$ for both reaction by 100mathrm~kJ~mol^-1$100\mathrm{~kJ~mol}^{-1}$, which of the following statement is correct?
A.textCatalyst does not alter the Gibbs energy change of a reaction.$\text{Catalyst does not alter the Gibbs energy change of a reaction.}$
B.textCatalyst can cause non-spontaneous reactions to occur.$\text{Catalyst can cause non-spontaneous reactions to occur.}$
C.textThe enthalpy change for the reaction is +20mathrm~kJ~mol^-1.$\text{The enthalpy change for the reaction is } +20\mathrm{~kJ~mol}^{-1}.$
D.textThe enthalpy change for the catalysed reaction is different from that of uncatalysed reaction.$\text{The enthalpy change for the catalysed reaction is different from that of uncatalysed reaction.}$
Solution
### Related Formula
Delta H = E_a(f) - E_a(b)$$\Delta H = E_{a(f)} - E_{a(b)}$$
### Core Logic
A catalyst accelerates both forward and backward path steps symmetrically by carving a lower activation energy profile route.
* Uncatalyzed values: Delta H = 180 - 200 = -20mathrm~kJ~mol^-1$\Delta H = 180 - 200 = -20\mathrm{~kJ~mol}^{-1}$.
* Catalyzed values: E_a(f)' = 80mathrm~kJ~mol^-1$E_{a(f)}' = 80\mathrm{~kJ~mol}^{-1}$ and E_a(b)' = 100mathrm~kJ~mol^-1$E_{a(b)}' = 100\mathrm{~kJ~mol}^{-1}$, leading to Delta H' = 80 - 100 = -20mathrm~kJ~mol^-1$\Delta H' = 80 - 100 = -20\mathrm{~kJ~mol}^{-1}$.
Thermodynamic parameters (Delta H$\Delta H$, Delta G$\Delta G$, Delta S$\Delta S$) depend strictly on the initial and final energy states of reactants and products, meaning they are completely unaltered by the presence of a catalyst.
### Pattern Recognition
Catalysts alter only kinetic properties (rate, activation barriers). They have zero impact on equilibrium positions or thermodynamic state parameters like Delta G$\Delta G$ or Delta H$\Delta H$.
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 12 Chemistry: Chemical Kinetics
Q33jee_main_2025_04_april_morningRate Law and Order
Rate law for a reaction between A and B is given by R = k[A]^n[B]^m$R = k[A]^n[B]^m$. If concentration of A is doubled and concentration of B is halved from their initial value, the ratio of new rate of reaction to the initial rate of reaction left(fracr_2r_1
ight)$\left(\frac{r_2}{r_1}
ight)$ is:
A.2^(n-m)$2^{(n-m)}$
B.(n-m)$(n-m)$
C.(m+n)$(m+n)$
D.frac12^m+n$\frac{1}{2^{m+n}}$
Solution
### Related Formula
r = k [A]^n [B]^m$$r = k [A]^n [B]^m$$
### Core Logic
Let the initial rate relation be:
r_1 = k [A]^n [B]^m$$r_1 = k [A]^n [B]^m$$
When concentration parameters shift ([A]' = 2[A]$[A]' = 2[A]$ and [B]' = frac[B]2$[B]' = \frac{[B]}{2}$):
r_2 = k (2[A])^n left(frac[B]2right)^m = k cdot 2^n [A]^n cdot 2^-m [B]^m$$r_2 = k (2[A])^n \left(\frac{[B]}{2}\right)^m = k \cdot 2^n [A]^n \cdot 2^{-m} [B]^m$$r_2 = 2^(n-m) cdot left(k [A]^n [B]^mright) = 2^(n-m) cdot r_1$$r_2 = 2^{(n-m)} \cdot \left(k [A]^n [B]^m\right) = 2^{(n-m)} \cdot r_1$$
Taking the ratio yields:
fracr_2r_1 = 2^(n-m)$$\frac{r_2}{r_1} = 2^{(n-m)}$$
### Pattern Recognition
Powers simplify cleanly via exponent rules: doubling a base scales the expression by 2^n$2^n$, while halving scales it by 2^-m$2^{-m}$.
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 12 Chemistry: Chemical Kinetics
More Chemical Kinetics Questions — jee_main_2025_28_jan_morning
We Map Every Repeating Question in Competitive Exams.
Say goodbye to generic mock test fatigue. RankBit uses smart analysis to group past exam questions into their foundational Repeating Question Types. Find chapter weightage, track repeating questions, and score higher with targeted practice.
Select Your Target Exam
Choose an exam track below to find formulas per chapter and patterns.
Syncing Exam Intelligence
Mapping formulas and patterns across all tracks…
PATH A — FULL LENGTH PRACTICE
Full Mock Test Hub
Simulate real NTA exam conditions with fully tracked mocks. Time yourself against past papers.
Practice past-year questions one chapter at a time. Pick an exam → subject → chapter and get every PYQ for that topic — pulled together from all past papers — with the chapter's key formulas alongside.