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For a first-order reaction, \(t_{0.9}\) is \(138.6\) seconds. Its specific reaction rate constant (in \(\left.\sec ^{-1}\right)\) is (a) \(10^{-2}\) (b) \(10^{-4}\) (c) \(10^{-5}\) (d) \(10^{-6}\)

Short Answer

Expert verified
The specific reaction rate constant is approximately \(10^{-4} \text{ sec}^{-1}\).

Step by step solution

01

Understand the Question

We are given a first-order reaction and are asked to find the specific reaction rate constant (k) based on the given value of \(t_{0.9}\), which is the time taken for the concentration of a reactant to decrease to 90% of its initial value.
02

Use First-Order Reaction Formula

For a first-order reaction, the relationship between the rate constant \(k\) and the time required for the concentration to decrease to a certain fraction of its original value is given by the formula: \[ t_x = \frac{2.303}{k} \log \left( \frac{1}{1-x} \right) \] Here, \(x = 0.1\) since we're considering the time to reach 90% of the initial concentration.
03

Substitute Given Values

We have \(t_{0.9} = 138.6\) seconds and \(x = 0.1\). Substitute these values into the formula:\[ 138.6 = \frac{2.303}{k} \log \left( \frac{1}{0.9} \right) \] Calculate the logarithm: \( \log \left( \frac{1}{0.9} \right) \approx 0.045757\).
04

Solve for Rate Constant k

Rearrange the equation to solve for \(k\):\[ k = \frac{2.303 \times 0.045757}{138.6} \] Calculate:\[ k \approx \frac{0.10527}{138.6} \approx 7.6 \times 10^{-4} \text{ sec}^{-1} \]
05

Choose the Correct Option

Compare the calculated \(k = 7.6 \times 10^{-4} \text{ sec}^{-1}\) with the given options:(a) \(10^{-2}\), (b) \(10^{-4}\), (c) \(10^{-5}\), and (d) \(10^{-6}\). The closest value to our calculation is \(10^{-4}\).

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Key Concepts

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

Rate Constant Calculation
To solve problems involving first-order reactions, it is important to calculate the rate constant, denoted as \( k \). The rate constant is a crucial parameter indicating how fast a reaction proceeds.
The formula to find \( k \) for a first-order reaction where the concentration decreases to a fraction \( x \) of its original value is given by:
  • \( t_x = \frac{2.303}{k} \log \left( \frac{1}{1-x} \right) \)
To solve for \( k \), you will first need to know two things:
  • The time \( t_x \) it takes to reach fraction \( x \)
  • The fraction \( x \) itself
By rearranging the formula, \( k \) can be calculated as follows:
  • \( k = \frac{2.303}{t_x} \log \left( \frac{1}{1-x} \right) \)
This formula essentially derives \( k \) by linking it to the percentage of reactant concentration remaining. In this specific problem, for example, \( t_{0.9} = 138.6 \) seconds is crucial for determining \( k \). Remember, knowing how to manipulate this basic formula is a doorway to solving various kinetics problems.
Reaction Kinetics
Understanding reaction kinetics is key to mastering how chemical reactions happen and at what speed. Reaction kinetics not only tells us about rate constants but also the mechanisms and sequences of steps involved.
A first-order reaction is straightforward: it relies on the concentration of a single reactant. The rate of reaction decreases exponentially over time as the reactant is consumed.
  • One particular characteristic of first-order reactions is their dependency on the concentration of one reactant only.
  • They have a constant half-life, meaning it takes the same amount of time for the concentration to fall from any initial amount to half of that, and then from half to one quarter, etc.
Being able to determine the rate constant helps us predict how the reaction will behave over time. Mastery of these kinetics rules is imperative for problem-solving in chemistry, and understanding their application can illuminate many experimentally observed phenomena.
Logarithmic Relationships in Chemistry
Logarithmic functions are often used in chemistry to express complex relationships efficiently. When dealing with first-order reactions, the logarithmic relationship provides a tool to link time and concentration changes.
The formula \( t_x = \frac{2.303}{k} \log \left( \frac{1}{1-x} \right) \) involves a logarithm to represent how remaining reactant concentrations affect reaction rates, a critical aspect to elucidate with logarithm properties:
  • The logarithm, \( \log \left( \frac{1}{1-x} \right) \), expresses how the remaining fraction of a reactant over its initial amount is related to the progression of the reaction.
  • It enables simplification because reactions often exhibit exponential decrease, and logarithms provide a linear method to express and calculate these trends accurately.
Always remember, grasp of logarithmic functions in chemistry extends beyond first-order reactions. They frequently arise in calculating pH in acid-base chemistry, examining light absorption in spectrophotometry, and more. Having a strong handle on logarithms equips you to tackle these challenges across different chemistry domains.

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Most popular questions from this chapter

For a chemical reaction which can never be a fractional number. (a) order (b) half-life (c) molecularity (d) rate constant

In a certain reaction \(8 \%\) of the reactant decomposes in 30 minutes, \(24 \%\) in 90 minutes and \(48 \%\) in 180 minutes. What are the dimensions of the rate constant? (a) Mol lit \(^{-1} \sec ^{-1}\) (b) \(\mathrm{Mol} \mathrm{sec}^{-1}\) (c) Lit \(\mathrm{mol}^{-1} \mathrm{sec}^{-1}\) (d) Hour \(^{-1}\)

The rate constant of a first-order reaction is \(6 \times 10^{-3}\) \(\mathrm{s}^{-1}\). If the initial concentration is \(0.10 \mathrm{M}\), the initial rate of reaction is (a) \(6 \times 10^{-3} \mathrm{Ms}^{-1}\) (b) \(6 \times 10^{-1} \mathrm{Ms}^{-1}\) (c) \(6 \times 10^{-6} \mathrm{Ms}^{-1}\) (d) \(6 \times 10^{-8} \mathrm{Ms}^{-1}\)

The slope of the line for the graph of \(\log k\) vs \(1 / T\) for the reaction, \(\mathrm{N}_{2} \mathrm{O}_{5} \longrightarrow 2 \mathrm{NO}_{2}+1 / 2 \mathrm{O}_{2}\) is \(-5000\). Calculate the energy of activation of the reaction. (a) \(95.7 \mathrm{~kJ} \mathrm{~mol}^{-1}\) (b) \(9.57 \mathrm{~kJ} \mathrm{~mol}^{-1}\) (c) \(957 \mathrm{~kJ} \mathrm{~mol}^{-1}\) (d) \(0.957 \mathrm{~kJ} \mathrm{~mol}^{-1} \mathrm{~K}^{-1}\)

During the decomposition of \(\mathrm{H}_{2} \mathrm{O}_{2}\) to give oxygen, \(48 \mathrm{~g} \mathrm{O}_{2}\) is formed per minute at a certain point of time. The rate of formation of water at this point is (a) \(0.75 \mathrm{~mol} \mathrm{~min}^{1}\) (b) \(1.5 \mathrm{~mol} \mathrm{~min}^{-1}\) (c) \(2.25 \mathrm{~mol} \mathrm{~min}^{-1}\) (d) \(3.0 \mathrm{~mol} \mathrm{~min}^{-1}\)

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