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For a first order reaction, the half life period is independent ofa. initial concentration b. cube root of initial concentration c. first power of final concentration d. square root of final concentration

Short Answer

Expert verified
The half-life is independent of initial concentration.

Step by step solution

01

Understanding Half-Life in First Order Reactions

The half-life (\( t_{1/2} \)) of a first-order reaction is the time it takes for the concentration of a reactant to decrease to half of its initial concentration. Importantly, for first-order reactions, this half-life is independent of the initial concentration.
02

Recognize the Key Characteristic of First Order Reactions

In a first-order reaction, the rate is proportional to the concentration of one reactant. The formula for the half-life of a first-order reaction is \( t_{1/2} = \frac{0.693}{k} \), where \( k \) is the rate constant. Notice that this expression does not include any term for the initial concentration.
03

Analysis of Answer Choices

From the given choices: a. Initial concentration, b. Cube root of initial concentration, c. First power of final concentration, and d. Square root of final concentration - only the initial concentration has no influence on the half-life for first order reactions. The other options involve modifications of concentration terms, which are not applicable to the half-life formula provided.
04

Concluding the Correct Answer

Based on the analysis, the half-life of a first-order reaction is independent of the initial concentration, since the formula for half-life (\( t_{1/2} = \frac{0.693}{k} \)) does not include any concentration terms. Thus, option (a) is correct.

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Key Concepts

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

Half-Life
The half-life of a chemical reaction is a key concept, especially in first-order reactions. It denotes the time required for the concentration of a reactant to reduce to half of its initial value. This measurement is crucial because it helps predict how long a reaction takes to reach a certain extent. In the context of first-order reactions, the half-life has a unique property: it remains constant regardless of the starting concentration of the reactant.

This is due to the mathematical expression for half-life, given by:\[t_{1/2} = \frac{0.693}{k}\]where \( t_{1/2} \) is the half-life and \( k \) is the rate constant. As you can see, the formula doesn't include any term that involves the concentration of the reactants.

Thus, the half-life for these reactions stays the same, regardless of how much reactant you start with. This distinguishes first-order reactions from other orders, where half-life may depend on the initial concentration.
Rate Constant
The rate constant, symbolized as \( k \), is a fundamental component of reaction kinetics. It is a measure of the speed of a reaction and is specific to each reaction under specified conditions such as temperature. For first-order reactions, the rate constant plays a crucial role in determining the half-life.

The relationship between the rate constant and the reaction rate in first-order kinetics is expressed as:\[\text{Rate} = k[A]\]where \([A]\) is the concentration of the reactant. In this expression, the rate is directly proportional to both the rate constant \( k \) and the concentration of the reactant.

This means that if \( k \) is higher, the reaction proceeds more quickly. This relationship also underpins the half-life equation \( t_{1/2} = \frac{0.693}{k} \). As you can see, the rate constant is inversely proportional to the half-life. This implies that a large rate constant results in a shorter half-life, indicating a faster reaction.
Reaction Kinetics
Reaction kinetics is the branch of chemistry that studies the speed or rate at which chemical reactions occur. It's fundamental to understanding how different factors like concentration, temperature, and catalysts affect the rates of reactions. In first-order reactions, kinetics have distinct characteristics that simplify analysis and prediction of reaction behavior.

In these reactions, the rate of reaction depends on the concentration of a single reactant raised to the power of one. This linear dependency means that the reaction rate changes proportionately with a change in reactant concentration.

Key features of first-order reaction kinetics include:
  • The reaction proceeds at a rate proportional to the single reactant’s concentration.
  • A constant half-life that does not vary with the concentration of the reactant.
  • The ability to use logarithmic functions to describe the rate, as evident in the equation:\[\text{ln} rac{[A]_0}{[A]} = kt\]where \([A]_0\) and \([A]\) are the initial and remaining concentrations of the reactant, and \( t \) is time elapsed.

    This equation can further simplify data analysis, as a plot of ln\([A]\) versus time yields a straight line with a slope equal to \(-k\). All these aspects collectively make first-order reactions predictable and easier to work with, aiding both theoretical studies and practical applications.

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Most popular questions from this chapter

The following set of data was obtained by the method of initial rates for the reaction: \(2 \mathrm{HgCl}_{2}(\mathrm{aq})+\mathrm{C}_{2} \mathrm{O}_{4}^{2-}(\mathrm{aq}) \rightarrow\) \(2 \mathrm{Cl}^{-}(\mathrm{aq})+2 \mathrm{CO}_{2}(\mathrm{~g})+\mathrm{Hg}_{2} \mathrm{Cl}_{2}(\mathrm{~s})\) What is the rate law for the reaction? \begin{tabular}{lll} \hline\(\left[\mathrm{HgCl}_{2}\right], \mathrm{M}\) & {\(\left[\mathrm{C}_{2} \mathrm{O}_{4}^{2-}\right], \mathrm{M}\)} & Rate, \(\mathrm{M} / \mathrm{s}\) \\ \hline \(0.10\) & \(0.10\) & \(1.3 \times 10^{-7}\) \\ \(0.10\) & \(0.20\) & \(5.2 \times 10^{-7}\) \\ \(0.20\) & \(0.20\) & \(1.0 \times 10^{-6}\) \\ \hline \end{tabular} a. Rate \(=\mathrm{k}\left[\mathrm{HgCl}_{2}\right]\left[\mathrm{C}_{2} \mathrm{O}_{4}^{2-}\right]^{2}\) b. Rate \(=\mathrm{k}\left[\mathrm{HgCl}_{2}\right]^{2}\left[\mathrm{C}_{2} \mathrm{O}_{4}^{2-}\right]\) c. Rate \(=\mathrm{k}\left[\mathrm{HgCl}_{2}\right]\left[\mathrm{C}_{2} \mathrm{O}_{4}^{2-}\right]^{2-}\) d. Rate \(=\mathrm{k}\left[\mathrm{HgCl}_{2}\right]\left[\mathrm{C}_{2} \mathrm{O}_{4}^{2-}\right]^{-1}\)

For the reaction \(\mathrm{W}+\mathrm{X} \rightarrow \mathrm{Y}+\mathrm{Z}\), the rate \((\mathrm{dx} / \mathrm{dt})\) when plotted against time ' \(\mathrm{t}\) ' gives a straight line parallel to time axis. The order and rate for this reaction are a. \(\mathrm{O}, \mathrm{K}\) b. \(1, \mathrm{~K}+1\) b. II, \(\mathrm{K}+1\) d. \(\mathrm{K}, \mathrm{K}+1\)

(A): Arrhenius equation explains the temperature dependence of rate of a chemical reaction. (R): Plots of log \(\mathrm{K}\) vs \(1 / \mathrm{T}\) are linear and the energy of activation is obtained from such plots.

What happens when the temperature of a reaction system is increased by \(10^{\circ} \mathrm{C}\) ? a. The effective number of collisions between the molecules possessing certain threshold energy increases atleast by \(100 \%\). b. The total number of collisions between reacting molecules increases atleast by \(100 \%\) c. The activation energy of the reaction is increased d. The total number of collisions between reacting molecules increases merely by \(1-2 \%\).

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

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