Match List I with List II
Choose the correct answer from the options given below: |
A-II, B-III, C-I, D-IV A-IV, B-III, C-I, D-II A-III, B-IV, C-II, D-I A-I, B-II, C-IV, D-III |
A-III, B-IV, C-II, D-I |
The correct answer is option 3. A-III, B-IV, C-II, D-I.
Let us delve into the details of each match in the context of chemical kinetics. A. Linear plot with +ve slope and an intercept: III. \(\frac{1}{[A]}\) vs time for the 2nd order For a second-order reaction, the integrated rate law can be expressed as: \(\frac{1}{[A]} = kt + \frac{1}{[A]_0}\) Here: \([A]\) is the concentration of the reactant at time \(t\), \(k\) is the rate constant, \([A]_0\) is the initial concentration of the reactant. This equation is of the form \(y = mx + c\), where: \(y = \frac{1}{[A]}\), \(x = t\), the slope \(m = k\) (which is positive for a second-order reaction), the intercept \(c = \frac{1}{[A]_0}\). A plot of \(\frac{1}{[A]}\) vs. \(t\) will give a straight line with a positive slope \(k\) and an intercept equal to \(\frac{1}{[A]_0}\).
B. Linear plot with -ve slope and an intercept: IV. Conc. \([A]\) vs time for zero order In a zero-order reaction, the concentration of the reactant \([A]\) decreases linearly with time. The rate of the reaction is independent of the concentration of the reactant, and the equation for a zero-order reaction can be expressed as: \([A] = [A]_0 - kt\) Where: \([A]\) is the concentration of the reactant at time \(t\). \([A]_0\) is the initial concentration of the reactant. \(k\) is the rate constant (with units of concentration/time). \(t\) is the time. This equation represents a straight line with: A negative slope equal to \(-k\). A y-intercept equal to \([A]_0\). The linear plot of \([A]\) vs. time will have a downward (negative) slope, indicating the decrease in concentration over time.
C. Linear horizontal plot: II. \(t_{1/2}\) vs \([A]_0\) for 1st order For a first-order reaction, the half-life \(\left(t_{1/2}\right)\) is independent of the initial concentration \([A]_0\). The formula for the half-life of a first-order reaction is: \(t_{1/2} = \frac{0.693}{k}\) Here, \(t_{1/2}\) is the half-life, and \(k\) is the rate constant. Since \(t_{1/2}\) does not depend on \([A]_0\), a plot of \(t_{1/2}\) versus \([A]_0\) for a first-order reaction will be a horizontal line, indicating that \(t_{1/2}\) remains constant regardless of the initial concentration.
D. Linear plot passing through the origin: I. \(t_{1/2}\) vs \(\frac{1}{[A]_0}\) for 2nd order For a second-order reaction, the half-life \(\left(t_{1/2}\right)\) is inversely proportional to the initial concentration \(\left([A]_0\right)\). The formula for the half-life of a second-order reaction is: \(t_{1/2} = \frac{1}{k[A]_0}\) Here: \(t_{1/2}\) is the half-life, \(k\) is the rate constant, \([A]_0\) is the initial concentration of the reactant. This equation can be rewritten as: \(t_{1/2} = \frac{1}{k} \times \frac{1}{[A]_0}\) This is of the form \(y = mx\), where: \(y = t_{1/2}\), \(x = \frac{1}{[A]_0}\), and the slope \(m = \frac{1}{k}\). A plot of \(t_{1/2}\) versus \(\frac{1}{[A]_0}\) for a second-order reaction will be a straight line that passes through the origin, with the slope equal to \(\frac{1}{k}\). Thus, the correct matching is option 3: A-III, B-IV, C-II, D-I. |