The first-order rate constant for the decomposition of \(\mathrm{N}_{2} \mathrm{O}_{5}, \quad 2 \mathrm{~N}_{2} \mathrm{O}_{5}(g) \longrightarrow 4 \mathrm{NO}_{2}(g)+\mathrm{O}_{2}(g), \quad\) at \(\quad 70^{\circ} \mathrm{C}\) is \(6.82 \times 10^{-3} \mathrm{~s}^{-1}\). Suppose we start with \(0.0250 \mathrm{~mol}\) of \(\mathrm{N}_{2} \mathrm{O}_{5}(g)\) in a volume of \(2.0 \mathrm{~L}\). (a) How many moles of \(\mathrm{N}_{2} \mathrm{O}_{5}\) will remain after \(5.0 \mathrm{~min} ?\) (b) How many minutes will it take for the quantity of \(\mathrm{N}_{2} \mathrm{O}_{5}\) to drop to \(0.010 \mathrm{~mol}\) ? (c) What is the half-life of \(\mathrm{N}_{2} \mathrm{O}_{5}\) at \(70{ }^{\circ} \mathrm{C} ?\)

Short Answer

Expert verified
(a) After 5.0 min, there will be approximately 0.0168 mol of N2O5 remaining. (b) It will take approximately 5.81 minutes for the quantity of N2O5 to drop to 0.010 mol. (c) The half-life of N2O5 at 70°C is approximately 1.70 minutes.

Step by step solution

01

Part A: Calculate moles of N2O5 remaining after 5.0 min

Given: Initial moles (A0) = 0.0250 mol Time (t) = 5.0 min = 300 s (converted to seconds) Rate constant (k) = 6.82 × 10^{-3} s^{-1} Use the formula: \[ ln(\frac{[A]_0}{[A]}) = kt \] Rearrange the formula to find the remaining moles (A): \[ [A] = \frac{[A]_0}{e^{kt}} \] Substitute the values: \[ [A] = \frac{0.0250}{e^{(6.82 × 10^{-3})(300)}} \] Calculate the result: \[ [A] = 0.0168 \; \text{mol} \] After 5.0 min, there will be approximately 0.0168 mol of N2O5 remaining.
02

Part B: Calculate time for the quantity of N2O5 to drop to 0.010 mol

Given: Initial moles (A0) = 0.0250 mol Final moles (A) = 0.010 mol Use the formula: \[ ln(\frac{[A]_0}{[A]}) = kt \] Rearrange the formula to find the time (t): \[ t = \frac{ln(\frac{[A]_0}{[A]})}{k} \] Substitute the values: \[ t = \frac{ln(\frac{0.0250}{0.010})}{6.82 × 10^{-3}} \] Calculate the result: \[ t ≈ 348.88 \; \text{s} \] Convert to minutes: \[ time \approx 5.81 \; \text{min} \] It will take approximately 5.81 minutes for the quantity of N2O5 to drop to 0.010 mol.
03

Part C: Calculate the half-life of N2O5 at 70°C

To find the half-life (t1/2) of a first-order reaction, we use the formula: \[ t_{1/2} = \frac{ln(2)}{k} \] Given: Rate constant (k) = 6.82 × 10^{-3} s^{-1} Substitute the value: \[ t_{1/2} = \frac{ln(2)}{6.82 × 10^{-3}} \] Calculate the result: \[ t_{1/2} ≈ 101.73 \; \text{s} \] Convert to minutes: \[ half-life ≈ 1.70 \; \text{min} \] The half-life of N2O5 at 70°C is approximately 1.70 minutes.

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Most popular questions from this chapter

Americium-241 is used in smoke detectors. It has a first order rate constant for radioactive decay of \(k=1.6 \times 10^{-3} \mathrm{yr}^{-1}\). By contrast, iodine- \(125,\) which is used to test for thyroid functioning, has a rate constant for radioactive decay of \(k=0.011\) day \(^{-1}\). (a) What are the halflives of these two isotopes? (b) Which one decays at a faster rate? (c) How much of a 1.00 -mg sample of each isotope remains after 3 half-lives? (d) How much of a 1.00 -mg sample of each isotope remains after 4 days?

A reaction \(A+B \longrightarrow C\) obeys the following rate law: Rate \(=k[\mathrm{~B}]^{2}\). (a) If \([\mathrm{A}]\) is doubled, how will the rate change? Will the rate constant change? Explain. (b) What are the reaction orders for \(\mathrm{A}\) and \(\mathrm{B}\) ? What is the overall reaction order? (c) What are the units of the rate constant?

Molecular iodine, \(\mathrm{I}_{2}(g)\), dissociates into iodine atoms at \(625 \mathrm{~K}\) with a first-order rate constant of \(0.271 \mathrm{~s}^{-1}\). (a) What is the half-life for this reaction? (b) If you start with \(0.050 \mathrm{M} \mathrm{I}_{2}\) at this temperature, how much will remain after 5.12 s assuming that the iodine atoms do not recombine to form \(\mathrm{I}_{2} ?\)

The oxidation of \(\mathrm{SO}_{2}\) to \(\mathrm{SO}_{3}\) is catalyzed by \(\mathrm{NO}_{2}\). The reaction proceeds according to: $$ \begin{array}{l} \mathrm{NO}_{2}(g)+\mathrm{SO}_{2}(g) \longrightarrow \mathrm{NO}(g)+\mathrm{SO}_{3}(g) \\ 2 \mathrm{NO}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{NO}_{2}(g) \end{array} $$ (a) Show that the two reactions can be summed to give the overall oxidation of \(\mathrm{SO}_{2}\) by \(\mathrm{O}_{2}\) to give \(\mathrm{SO}_{3}\). (b) Why do we consider \(\mathrm{NO}_{2}\) a catalyst and not an intermediate in this reaction? (c) Is this an example of homogeneous catalysis or heterogeneous catalysis?

(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 \(0.036 \mathrm{M} / \mathrm{s}\), 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 74 torr per hour. What are the rates of change of \(\mathrm{NH}_{3}\) partial pressure and total pressure in the vessel?

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