(a) For the generic reaction \(\mathrm{A} \rightarrow \mathrm{B}\) what quantity, when graphed versus time, will yield a straight line for a first- order reaction? (b) How can you calculate the rate constant for a first-order reaction from the graph you made in part (a)?

Short Answer

Expert verified
(a) For a first-order reaction, plotting \(\ln[A]\) versus time (t) will yield a straight line. The equation for this linear relationship is \(\ln[A] = -kt + \ln[A]_0\). (b) To calculate the rate constant (k) for a first-order reaction from the graph, use the slope of the straight line representing the relationship between ln[A] and time. The rate constant k is the negative of the slope: k = -slope.

Step by step solution

01

Part (a): Identify the linear form for the first-order reaction

For a first-order reaction, the rate of reaction is directly proportional to the concentration of the reactant A. The rate equation can be written as: \(r = k [A]\) where r is the rate of reaction, k is the rate constant, and [A] is the concentration of A. To find a linear relationship for this reaction, we will use the integrated rate law for a first-order reaction: \(\ln[A] = -kt + \ln[A]_0\) where [A] is the concentration of A at time t, and [A]₀ is the initial concentration of A. This equation resembles the formula for a straight line (y = mx + b), where: - y = \(\ln[A]\) - m = -k - x = t - b = \(\ln[A]_0\) Thus, plotting ln[A] versus time (t) will yield a straight line for a first-order reaction.
02

Part (b): Calculate the rate constant from the graph

Now that we've determined that the linear relationship for a first-order reaction involves plotting ln[A] versus time, we can use the slope of the straight line from the graph to calculate the rate constant (k). As previously stated, the equation of the straight line for the first-order reaction is: \(\ln[A] = -kt + \ln[A]_0\) From this equation, we can see that the slope of the straight line (-k) is the rate constant multiplied by -1. To calculate the rate constant k, we take the negative of the slope of the straight line from the graph, which is the relationship between ln[A] and time: k = -slope So, by plotting ln[A] versus time for a first-order reaction, we can obtain the rate constant k by taking the negative of the slope of the resulting straight line.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

(a) Consider the combustion of ethylene, \(\mathrm{C}_{2} \mathrm{H}_{4}(g)+\) $3 \mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{CO}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(g) .\( If the concentration of \)\mathrm{C}_{2} \mathrm{H}_{4}$ is decreasing at the rate of \(0.025 \mathrm{M} / \mathrm{s}\), what are the rates of change in the concentrations of \(\mathrm{CO}_{2}\) and $\mathrm{H}_{2} \mathrm{O}\( ? (b) The rate of decrease in \)\mathrm{N}_{2} \mathrm{H}_{4}$ partial pressure in a closed reaction vessel from the reaction $\mathrm{N}_{2} \mathrm{H}_{4}(g)+\mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{NH}_{3}(g)$ is \(10 \mathrm{kPa}\) per hour. What are the rates of change of \(\mathrm{NH}_{3}\) partial pressure and total pressure in the vessel?

(a) In which of the following reactions would you expect the orientation factor to be more important in leading to reaction: $\mathrm{O}_{3}+\mathrm{O} \longrightarrow 2 \mathrm{O}_{2}\( or \)\mathrm{NO}+\mathrm{NO}_{3} \longrightarrow 2 \mathrm{NO}_{2} ?$ (b) What is related to the orientation factor? Which, smaller or larger ratio of effectively oriented collisions to all possible collisions, would lead to a smaller orientation factor?

(a) Most commercial heterogeneous catalysts are extremely finely divided solid materials. Why is particle size important? (b) What role does adsorption play in the action of a heterogeneous catalyst?

Consider the reaction \(2 \mathrm{~A} \longrightarrow \mathrm{B}\). Is each of the following statements true or false? (a) The rate law for the reaction must be, Rate \(=k[\mathrm{~A}]^{2} .(\mathbf{b})\) If the reaction is an elementary reaction, the rate law is second order. \((\mathbf{c})\) If the reaction is an elementary reaction, the rate law of the reverse reaction is first order. (d) The activation energy for the reverse reaction must be smaller than that for the forward reaction.

(a) The reaction $\mathrm{C}_{12} \mathrm{H}_{22} \mathrm{O}_{11}(a q)+\mathrm{H}_{2} \mathrm{O}(l) \rightarrow \mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}(a q)+\( \)\mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}(a q)$ is first order with in \(\mathrm{C}_{12} \mathrm{H}_{22} \mathrm{O}_{11}(a q)\) and zero-order in \(\mathrm{H}_{2} \mathrm{O}\). At \(300 \mathrm{~K}\) the rate constant equals \(3.30 \times 10^{-2} \mathrm{~min}^{-1} .\) Calculate the half- life at this temperature. \((\mathbf{b})\) If the activation energy for this reaction is \(80.0 \mathrm{~kJ} / \mathrm{mol}\), at what temperature would the reaction rate be doubled?

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free