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The reaction \(\mathrm{A} \rightarrow \mathrm{B}\) follows first order kinetics. The time taken for \(0.8\) mole of \(\mathrm{A}\) to produce \(0.6\) mole of \(\mathrm{B}\) is 1 hour. What is the time taken for conversion of \(0.9\) mole of A to produce \(0.675\) mole of \(\mathrm{B} ?\) a. 2 hours b. 1 hour c. \(0.5\) hour d. \(0.25\) hour

Short Answer

Expert verified
The time taken is 1 hour, matching option (b).

Step by step solution

01

Determine Initial Conditions for First Reaction

In the first reaction, we start with 0.8 moles of A. We know that 0.6 moles of A have converted to B. Thus, the change in concentration of A, expressed as the concentration of A remaining, is the initial minus the final concentration of B produced.The initial moles of A is 0.8, and after producing 0.6 moles of B:\[ [A]_{final} = 0.8 - 0.6 = 0.2 \text{ moles of A remaining} \]
02

Calculate Rate Constant (k)

For first-order reactions, the rate equation is:\[ k = \frac{1}{t} \ln \left(\frac{[A]_0}{[A]}\right) \]Using the first reaction data:\[ t = 1 \text{ hour}, [A]_0 = 0.8, [A] = 0.2 \]Plugging in these values:\[ k = \frac{1}{1} \ln \left(\frac{0.8}{0.2}\right) = \ln(4) \]
03

Determine Initial Conditions for Second Reaction

Now the initial moles of A for the second reaction is 0.9 and it produces 0.675 moles of B. Thus:\[ [A]_{final} = 0.9 - 0.675 = 0.225 \text{ moles of A remaining} \]
04

Calculate Time for Second Reaction

Using the same first-order rate equation to solve for the new time (t):\[ k = \ln(4) \]\[ t = \frac{1}{k} \ln \left(\frac{[A]_0}{[A]}\right) \]Plug in the values for the second case:\[ t = \frac{1}{\ln(4)} \ln \left(\frac{0.9}{0.225}\right) \]\[ t = \frac{1}{\ln(4)} \ln(4) \]\[ t = 1 \text{ hour} \]
05

Choose the Correct Answer

Comparing our calculation with the options given. The calculated time for the second reaction is 1 hour, matching option (b). Thus, the answer to the exercise is option (b): 1 hour.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Reaction Rate Constant
In first-order kinetics, the reaction rate constant (k) is a crucial parameter. It helps predict how fast a chemical reaction will proceed. To determine this constant, we use the relationship of concentration and time. For a first-order reaction like \(\mathrm{A} \rightarrow \mathrm{B}\), the formula is:
  • \[ k = \frac{1}{t} \ln \left(\frac{[A]_0}{[A]}\right) \]
Here, \(k\) is the rate constant, \(t\) is the time, \([A]_0\) is the initial concentration of reactant A, and \([A]\) is the concentration of A after time \(t\).
For our exercise, we calculated \(k\) using known values: \(t = 1\) hour, \([A]_0 = 0.8\) moles, and \([A] = 0.2\) moles, which gave us \(k = \ln(4)\). This value allows us to predict how long the second reaction should take.
Mole Conversion
Mole conversion is a fundamental concept in chemical reactions. It involves determining how many moles of one substance react with or produce another substance. In our reaction \( \mathrm{A} \to \mathrm{B}\), we perform a mole conversion to find out how many moles of A convert to B.
  • Initially, 0.8 moles of \(A\) are present. 0.6 moles convert to \(B\), leaving 0.2 moles of \(A\).
  • For the second scenario, 0.9 moles of \(A\) are used. 0.675 moles are converted to \(B\), leaving 0.225 moles of \(A\) remaining.
By understanding the change in moles, we can calculate remaining reactants or predict product formation in a reaction. It's a crucial step before applying the rate constant formula.
Time Calculation
The calculation of time required for a specific amount of reactant to convert into product is central to kinetics. In first-order reactions, once the reaction rate constant \(k\) is known, we can calculate the time for any conversion using:
  • \[ t = \frac{1}{k} \ln \left(\frac{[A]_0}{[A]}\right) \]
This formula rearranges the rate law to solve for \(t\). By substituting the initial and remaining concentrations of A for the second scenario, we predict the time specific to that condition.
The constant \(k\) calculated from initial reaction conditions (\[k = \ln(4)\]) is used again to confirm that the time for 0.9 moles to convert 0.675 moles of B is indeed 1 hour. This demonstrates the consistency and predictive power of kinetic equations.
IIT JEE Physical Chemistry Problems
When tackling IIT JEE physical chemistry problems, having a strong grasp of kinetics is vital. These exams often test not only formulas but also understanding.
In this exercise, we used several significant concepts:
  • Understanding rates of reaction through reaction constants.
  • Converting moles to relate to reactants and products.
  • Calculating the time from rate constants and mole conversions.
It's crucial to remember these steps and concepts:
  • Grasp initial information and conditions clearly.
  • Utilize formulas appropriately.
  • Apply logical problem-solving skills to interpret the results.
Competence in these areas will aid in tackling diverse problems under exam conditions effectively, especially for the IIT JEE, which emphasizes precision and comprehension in physical chemistry.

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Most popular questions from this chapter

Which of the following statements are true about reaction mechanisms? (I) A rate law can be written from the molecularity of the slowest elementary step. (II) The final rate law can include intermediates. (III) The rate of the reaction is dependent on the fastest step in the mechanism. (IV) A mechanism can never be proven to be the correct pathway for a reaction. a. I and II b. I and IV c. II and III d. I. II and III

The equation tris(1,10-phenanthroline) iron(II) in acid solution takes place according to the equation: \(\mathrm{Fe}(\text { phen })_{3}^{2+}+3 \mathrm{H}_{3} \mathrm{O}^{+}+3 \mathrm{H}_{2} \mathrm{O} \rightarrow\) $$ \left.\mathrm{Fe}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}{ }^{2+}+3 \text { (Phen }\right) \mathrm{H}^{+} $$ If the activation energy (Ea) is \(126 \mathrm{~kJ} / \mathrm{mol}\) and the rate constant at \(30^{\circ} \mathrm{C}\) is \(9.8 \times 10^{-3} \mathrm{~min}^{-1}\), what is the frequency factor (A)? a. \(9.5 \times 10^{18} \mathrm{~min}^{-1}\) b. \(2.5 \times 10^{19} \mathrm{~min}^{-1}\) c. \(55 \times 10^{19} \mathrm{~min}^{-1}\) d. \(5.0 \times 10^{19} \mathrm{~min}^{-1}\)

(A): Order of reaction is an experimental property and irrespective of the fact whether the reaction is elementary or complicated, it is the sum of the powers of the concentration terms appearing in the rate law that is, experimentally observed rate law. (R): Order of reaction may change with change in experimental conditions.

Which of the following statement about the Arrhenius equation is/are correct? a. On raising temperature, rate constant of the reaction of greater activation energy increases less rapidly than that of the reaction of smaller activation energy. b. The term \(\mathrm{e}^{-\mathrm{Ea} \mathrm{RT}}\) represents the fraction of the molecules having energy in excess of threshold value. c. The pre-exponential factor becomes equal to the rate constant of the reaction at extremely high temperature. d. When the activation energy of the reaction is zero, the rate becomes indenendent of temnerature

(A): A catalyst enhances the rate of reaction. (R) : The energy of activation of the reaction is lowered in presence of a catalyst.

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