Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

The rate law for the decomposition of phosphine \(\left(\mathrm{PH}_{3}\right)\) is $$\text { Rate }=-\frac{\Delta\left[\mathrm{PH}_{3}\right]}{\Delta t}=k\left[\mathrm{PH}_{3}\right]$$ It takes \(120 .\) s for \(1.00 M\) PH \(_{3}\) to decrease to 0.250 M. How much time is required for \(2.00\space \mathrm{M} \mathrm{PH}_{3}\) to decrease to a concentration of \(0.350\space \mathrm{M} ?\)

Short Answer

Expert verified
It takes approximately 200 seconds for a 2.00 M concentration of PH3 to decrease to a concentration of 0.350 M.

Step by step solution

01

Determine the rate constant (k) using the given data

We can use the integrated rate law for a first-order reaction to solve this exercise. The integrated rate law for a first-order reaction is given by: \[ \ln\left(\frac{[\mathrm{PH}_{3}]_{0}}{[\mathrm{PH}_{3}]_{t}}\right) = kt \] where \([PH_3]_0\) is the initial concentration, \([PH_3]_t\) is the concentration at time t, k is the rate constant, and t is the time. We can use the data given in the exercise to calculate the rate constant (k). The initial concentration is 1.00 M, it decreases to 0.250 M after 120 s. Plug in the values and solve for k: \[ \ln\left(\frac{1.00\: \mathrm{M}}{0.250\: \mathrm{M}}\right) = k(120 \:s) \]
02

Calculating k

Calculate k. \[ k = \frac{\ln\left(\frac{1.00\: \mathrm{M}}{0.250\: \mathrm{M}}\right)}{120 \:s} \] \[ k \approx 0.00577\: \mathrm{s}^{-1} \]
03

Use the rate constant to find the time for the new initial concentration

Now that we have the rate constant k, we can use it to find the time required for a 2.00 M concentration of PH3 to decrease to 0.350 M. Plug in the values and solve for t: \[ \ln\left(\frac{2.00\: \mathrm{M}}{0.350\: \mathrm{M}}\right) = (0.00577 \: \mathrm{s}^{-1})t\]
04

Calculating t

Calculate t. \[ t = \frac{\ln\left(\frac{2.00\: \mathrm{M}}{0.350\: \mathrm{M}}\right)}{0.00577 \: \mathrm{s}^{-1}} \] \[ t \approx 199.99 \: \mathrm{s} \] The time required for a 2.00 M concentration of PH3 to decrease to a concentration of 0.350 M is approximately 200 seconds.

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!

Key Concepts

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

Rate Law
In reaction kinetics, the rate law is an essential concept that helps us understand how the concentration of reactants affects the rate of a chemical reaction. It expresses the rate of a chemical reaction as a function of the concentration of its reactants. For a reaction involving phosphine (PH₃), the rate law is given by the equation:
\[ \text{Rate} = -\frac{\Delta[\text{PH}_3]}{\Delta t} = k [\text{PH}_3] \]
This rate law indicates that the rate of decomposition of phosphine is directly proportional to its concentration. The proportionality constant in this equation, \( k \), is known as the rate constant. Understanding the rate law is crucial in predicting how changes in concentration impact the speed of reactions. It helps chemists to control the conditions under which reactions proceed.
First-Order Reaction
A first-order reaction is a type of reaction where the rate depends linearly on the concentration of a single reactant. In our example, the decomposition of phosphine is a first-order reaction, meaning that the rate directly depends on the concentration of \( [\text{PH}_3] \). The mathematical representation of a first-order reaction is:
\[ \text{Rate} = k [\text{PH}_3] \]
In first-order reactions, as the concentration of the reactant decreases, the rate of reaction also decreases at the same proportional rate. These reactions are common in nature and play an essential role in processes such as radioactive decay and many biological mechanisms. Understanding first-order reactions helps in determining how long a reaction will take to proceed to a certain level of completion.
Integrated Rate Law
The integrated rate law is a derived form of the rate law that links concentration with time, allowing us to calculate how long it takes for a reaction to reach a certain concentration. For a first-order reaction, the integrated rate law is given by:
\[ \ln\left(\frac{[\text{PH}_3]_0}{[\text{PH}_3]_t}\right) = kt \]
This equation is invaluable when determining the remaining concentration at a given time, or vice versa. By rearranging the equation, we can find either the time or concentration, depending on the known parameters. It becomes particularly useful when assessing the time required for significant concentration changes. In our phosphine decomposition example, we use the integrated rate law to determine how much time is required for the concentration to decrease from an initial to a specific value.
Rate Constant
The rate constant \( k \) is a critical factor in the rate law equation, representing the speed at which a reaction occurs. It remains constant for a given reaction at a specific temperature. In a first-order reaction, the units of the rate constant are \( \text{s}^{-1} \), signifying it's time-dependent.
To find \( k \), we used the integrated rate law and known concentrations and times. Calculating \( k \) correctly allows us to predict how fast a reaction will proceed under set conditions. Knowing the rate constant is essential for chemists, as it provides insight into the reaction's dynamics and how altering conditions, like temperature or concentration, may accelerate or decelerate the process.

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

Consider the following statements: "In general, the rate of a chemical reaction increases a bit at first because it takes a while for the reaction to get "warmed up.' After that, however, the rate of the reaction decreases because its rate is dependent on the concentrations of the reactants, and these are decreasing." Indicate everything that is correct in these statements, and indicate everything that is incorrect. Correct the incorrect statements and explain.

The decomposition of ethanol \(\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\right)\) on an alumina \(\left(\mathrm{Al}_{2} \mathrm{O}_{3}\right)\) surface$$\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(g) \longrightarrow \mathrm{C}_{2} \mathrm{H}_{4}(g)+\mathrm{H}_{2} \mathrm{O}(g)$$was studied at 600 K. Concentration versus time data were collected for this reaction, and a plot of \([\mathrm{A}]\) versus time resulted in a straight line with a slope of \(-4.00 \times 10^{-5} \mathrm{mol} / \mathrm{L} \cdot \mathrm{s}\) a. Determine the rate law, the integrated rate law, and the value of the rate constant for this reaction. b. If the initial concentration of \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\) was \(1.25 \times 10^{-2}\) \(M,\) calculate the half-life for this reaction. c. How much time is required for all the \(1.25 \times 10^{-2} M\) \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\) to decompose?

The activation energy for some reaction $$\mathrm{X}_{2}(g)+\mathrm{Y}_{2}(g) \longrightarrow 2 \mathrm{XY}(g)$$ is \(167 \mathrm{kJ} / \mathrm{mol},\) and \(\Delta E\) for the reaction is \(+28 \mathrm{kJ} / \mathrm{mol} .\) What is the activation energy for the decomposition of XY?

The activation energy for a reaction is changed from \(184 \space\mathrm{kJ} /\) mol to \(59.0 \space\mathrm{kJ} / \mathrm{mol}\) at \(600 .\) K by the introduction of a catalyst. If the uncatalyzed reaction takes about 2400 years to occur, about how long will the catalyzed reaction take? Assume the frequency factor \(A\) is constant, and assume the initial concentrations are the same.

Consider a reaction of the type aA \(\longrightarrow\) products, in which the rate law is found to be rate \(=k[\mathrm{A}]^{3}\) (termolecular reactions are improbable but possible). If the first half-life of the reaction is found to be \(40 .\) s, what is the time for the second half-life? Hint: Using your calculus knowledge, derive the integrated rate law from the differential rate law for a termolecular reaction: $$\text { Rate }=\frac{-d[\mathrm{A}]}{d t}=k[\mathrm{A}]^{3}$$

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