A first order reaction takes \(69.3\) minutes for \(50 \%\) completion. How much time will be needed for \(80 \%\) completion?

Short Answer

Expert verified
The time needed for 80% completion of a first order reaction can be calculated using the rate constant derived from the known 50% completion time.

Step by step solution

01

Understand the Basic Concept of a First Order Reaction

For a first order reaction, the time required to consume a certain percentage of the reactant is proportional to the negative natural logarithm of the fraction of reactant remaining. This can be shown by the formula: \( t = \frac{1}{k} \ln\left(\frac{1}{1 - x}\right) \), where \( t \) is the time, \( k \) is the first order rate constant, and \( x \) is the fraction of reactant completed at time \( t \).
02

Calculate the Rate Constant \( k \)

Using the given information that the reaction takes 69.3 minutes for 50% completion, we can calculate \( k \) by substituting \( x = 0.5 \) (since 50% completed) and \( t = 69.3 \) minutes into the formula: \[ k = \frac{1}{t} \ln\left(\frac{1}{1 - x}\right) = \frac{1}{69.3} \ln\left(\frac{1}{1 - 0.5}\right) \].
03

Determine the Time for 80% Completion

With \( k \) known from Step 2, we can now find the time for 80% completion, where \( x = 0.8 \). Substituting \( k \) and \( x = 0.8 \) into our first order reaction formula gives us: \[ t = \frac{1}{k} \ln\left(\frac{1}{1 - 0.8}\right) \]. Solve for time \( t \) to get the required time for 80% completion.
04

Perform the Calculations

First solve for the rate constant \( k \) using the values from Step 2, then use this rate constant to calculate the time for 80% completion from Step 3. Calculate \( k \) and substitute it and \( x = 0.8 \) back into the equation to find the final time.

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Key Concepts

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

Rate Constant Calculation
The rate constant, denoted as k, is a crucial number in chemical kinetics as it provides the speed at which a reaction proceeds. To compute the rate constant for a first-order reaction, we use the relationship:

\[\begin{equation}k = \frac{1}{t} \ln(\frac{1}{1 - x})\end{equation}\]

where
  • t is the time taken for the reaction to reach a certain level of completion, and
  • x is the fraction of reactant that has been converted at time t. For instance, if 50% of the reactant is consumed, x would be 0.5.

When t and x are known, as in the exercise problem at hand, the rate constant k can be calculated. In essence, it is a measure of the reaction's progress per unit time, and its unit is reciprocal of the time unit used, such as min-1 or s-1. Knowing k is pivotal because it allows us to predict the time required for different levels of reaction completion and is a fundamental step in solving many IIT-JEE chemistry problems.
Half-Life of Reaction
The concept of half-life is widely used in describing first-order reactions. The half-life of a reaction, typically represented as t1/2, is the time required for half of the reactant to be converted into products. For a first-order reaction, the half-life is constant and is given by the formula:

\[\begin{equation} t_{1/2} = \frac{0.693}{k}\end{equation}\]

where k is the rate constant. A prominent feature of first-order reactions is that their half-life does not depend on the initial concentration of reactants. This particularity makes calculations involving half-lives very convenient, as the same amount of time will pass for each successive half of the reactant to decompose, regardless of how much reactant is left.
Natural Logarithm in Kinetics
The natural logarithm plays a significant role in the kinetics of chemical reactions, especially first-order reactions. It is an intrinsic part of the formula used to calculate the rate constant and, subsequently, the time taken for a certain level of reaction completion.

\[\begin{equation} t = \frac{1}{k} \ln(\frac{1}{1 - x})\end{equation}\]

In this equation, we take the natural logarithm of the inverse of one minus the fraction completed (x). This mathematical operation allows us to linearize the exponential decay of reactant concentration over time, which is a characteristic of first-order kinetics. Understanding how the natural logarithm is used in reaction kinetics is vital, not just for tackling textbook problems but also for interpreting experimental data in real-world scenarios.
IIT-JEE Chemistry Problems
In the context of IIT-JEE, one of India’s most challenging engineering entrance exams, chemistry problems often assess a student’s understanding of fundamental concepts, including reaction kinetics. First-order reaction calculations are a common topic in these competitive exams.

Applying the concepts of rate constant calculation, half-life, and the use of natural logarithms can help solve problems regarding reaction times and the extent of completion. Students are expected to seamlessly integrate these concepts to efficiently work through the problems, applying mathematical manipulations where necessary. For example, by utilizing the concept of half-life, a student might bypass the need to calculate the rate constant directly when the problem pertains to the time taken for half of the reactant to react. Familiarity and fluency with these topics enable students to tackle a wide array of IIT-JEE chemistry problems with confidence.

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Most popular questions from this chapter

The decomposition of \(\mathrm{N}_{2} \mathrm{O}_{5}\) takes place according to I order as $$ 2 \mathrm{~N}_{2} \mathrm{O}_{5} \longrightarrow 4 \mathrm{NO}_{2}+\mathrm{O}_{2} $$ Calculate : (a) The rate constant, if instantaneous rate is \(1.4 \times 10^{-6}\) mol litre \(^{-1}\) \(\mathrm{sec}^{-1}\) when concentration of \(\mathrm{N}_{2} \mathrm{O}_{5}\) is \(0.04 \mathrm{M}\) (b) The rate of reaction when concentration of \(\mathrm{N}_{2} \mathrm{O}_{5}\) is \(1.20 \mathrm{M}\) (c) The concentration of \(\mathrm{N}_{2} \mathrm{O}_{5}\) when the rate of reaction will be \(2.45 \times 10^{-5} \mathrm{~mol}\) litre \(^{-1} \mathrm{sec}^{-\mathrm{i}}\).

From the rate expression for the following reactions, determine their order of renction and the dimensions of the rate constants. (u) \(\mathrm{WNO}_{(\mathrm{k})} \cdots \mathrm{N}_{2} \mathrm{O}_{(\mathrm{g})}+\mathrm{NO}_{2(\mathrm{~g})} ; \quad\) Rate \(=K[\mathrm{NO}]^{2}\) Rate \(=K\left[\mathrm{H}_{2} \mathrm{O}_{2}\right][\mathrm{I}]\) (c) \(\mathrm{CH}_{3} \mathrm{CHO}_{(\mathrm{g})} \longrightarrow \mathrm{CH}_{4(\mathrm{~g})}+\mathrm{CO}_{(\mathrm{g})} ;\) Rate \(=K\left[\mathrm{CH}_{3} \mathrm{CHO}\right]^{3 / 2}\) (d) \(\mathrm{CHCl}_{3(\mathrm{~g})}+\mathrm{Cl}_{2(g)} \longrightarrow \mathrm{CCl}_{4(\mathrm{~g})}+\mathrm{HCl}_{(\mathrm{g})}\) Rate \(=K\left[\mathrm{CHCl}_{3}\right]\left[\mathrm{Cl}_{2}\right]^{1 / 2}\)

A reaction is first order in \(A\) and second order in \(B\) : (i) Write differential rate equation. (ii) How is the rate affected when the concentration of \(B\) is tripled? (iii) How is the rate affected when the concentration of both \(A\) and \(B\) is doubled?

The reaction; \(2 \mathrm{~N}_{2} \mathrm{O}_{5} \longrightarrow 4 \mathrm{NO}_{2}+\mathrm{O}_{2}\), shows an increase in concentration of \(\mathrm{NO}_{2}\) by \(20 \times 10^{-3}\) mol litre \(^{-1}\) in 5 second. Calculate (a) rate of appearance of \(\mathrm{NO}_{2}\), (b) rate of reaction and (c) rate of disappearance of \(\mathrm{N}_{2} \mathrm{O}_{5}\).

Thermal decomposition of a compound is of first order. If \(50 \%\) sample of the compound is decomposed in 120 minute, how long will it take for \(90 \%\) of the compound to decompose?

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