The first-order rate constant for the decomposition of $\mathrm{N}_{2} \mathrm{O}_{5}, 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} .(\mathbf{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) There will be \(0.0190\) moles of N2O5 remaining after \(5\) minutes. (b) It will take approximately \(7.42\) minutes for the quantity of N2O5 to drop to \(0.010 \,\text{mol}\). (c) The half-life of N2O5 at \(70^{\circ} \mathrm{C}\) is approximately \(1.7\) minutes.

Step by step solution

01

(a) Moles of N2O5 remaining after 5 minutes

We are given the initial concentration and the rate constant for the decomposition of N2O5. We will use the first-order rate law equation to calculate the remaining amount of N2O5 after 5 minutes: \[a_t = a_0e^{-kt}\] where: - \(a_t\) is the amount of N2O5 at time t - \(a_0\) is the initial amount of N2O5 - k is the first-order rate constant (6.82 x 10^-3 s^-1) - t is the time (5 minutes = 300 seconds) Plugging the values into the equation, we have: \[a_t = (0.0250) e^{-(6.82 \times 10^{-3})(300)}\] Calculating the result, we get: \[a_t = 0.0190 \,\text{mol}\] Hence, there will be 0.0190 moles of N2O5 remaining after 5 minutes.
02

(b) Time to drop the quantity of N2O5 to 0.010 mol

We will use the same first-order rate law equation to find the time it takes for the amount of N2O5 to reach 0.010 mol. Rearranging the equation to solve for time: \[t = -\frac{\ln(\frac{a_t}{a_0})}{k}\] Plugging the values into the equation, we have: \[t = -\frac{\ln(\frac{0.010}{0.0250})}{6.82 \times 10^{-3}}\] Calculating the result, we get: \[t = 445 \,\text{seconds}\] Converting the time to minutes, we have: \[\text{Time} = \frac{445}{60} \, \text{min}\] Hence, it will take approximately 7.42 minutes for the quantity of N2O5 to drop to 0.010 mol.
03

(c) Half-life of N2O5 at 70°C

The half-life of a first-order reaction can be determined using the following equation: \[t_{1/2} = \frac{0.693}{k}\] We already have the rate constant, so plugging the value into the equation, we get: \[t_{1/2} = \frac{0.693}{6.82 \times 10^{-3}}\] Calculating the result, we get: \[t_{1/2} = 102 \, \text{seconds}\] Converting this to minutes, we have: \[\text{Half-Life} = \frac{102}{60} \, \text{min}\] Hence, the half-life of N2O5 at 70°C is approximately 1.7 minutes.

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Most popular questions from this chapter

Consider the following hypothetical aqueous reaction: $\mathrm{A}(a q) \rightarrow \mathrm{B}(a q)\(. A flask is charged with \)0.065 \mathrm{~mol}$ of \(\mathrm{A}\) in a total volume of \(100.0 \mathrm{~mL}\). The following data are collected: $$ \begin{array}{lccccc} \hline \text { Time (min) } & 0 & 10 & 20 & 30 & 40 \\ \hline \text { Moles of A } & 0.065 & 0.051 & 0.042 & 0.036 & 0.031 \\ \hline \end{array} $$ (a) Calculate the number of moles of \(\mathrm{B}\) at each time in the table, assuming that there are no molecules of \(\mathrm{B}\) at time zero and that A cleanly converts to B with no intermediates. (b) Calculate the average rate of disappearance of A for each 10 -min interval in units of \(M /\) s. (c) Between \(t=0 \mathrm{~min}\) and \(t=30 \mathrm{~min},\) what is the average rate of appearance of \(\mathrm{B}\) in units of \(\mathrm{M} / \mathrm{s}\) ? Assume that the volume of the solution is constant.

The oxidation of \(\mathrm{SO}_{2}\) to \(\mathrm{SO}_{3}\) is accelerated 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, with appropriate coefficients, 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) Do we consider \(\mathrm{NO}_{2}\) a catalyst or an intermediate in this reaction? (c) Would you classify NO as a catalyst or as an intermediate? (d) Is this an example of homogeneous catalysis or heterogeneous catalysis?

The gas-phase reaction of \(\mathrm{NO}\) with \(\mathrm{F}_{2}\) to form \(\mathrm{NOF}\) and \(\mathrm{F}\) has an activation energy of $E_{a}=6.3 \mathrm{~kJ} / \mathrm{mol}\(. and a frequency factor of \)A=6.0 \times 10^{8} M^{-1} \mathrm{~s}^{-1}$. The reaction is believed to be bimolecular: $$ \mathrm{NO}(g)+\mathrm{F}_{2}(g) \longrightarrow \mathrm{NOF}(g)+\mathrm{F}(g) $$ (a) Calculate the rate constant at \(100^{\circ} \mathrm{C}\). (b) Draw the Lewis structures for the \(\mathrm{NO}\) and the NOF molecules, given that the chemical formula for NOF is misleading because the nitrogen atom is actually the central atom in the molecule. (c) Predict the shape for the NOF molecule. (d) Draw a possible transition state for the formation of NOF, using dashed lines to indicate the weak bonds that are beginning to form. (e) Suggest a reason for the low activation energy for the reaction.

Consider the following reaction: $$ 2 \mathrm{NO}(g)+2 \mathrm{H}_{2}(g) \longrightarrow \mathrm{N}_{2}(g)+2 \mathrm{H}_{2} \mathrm{O}(g) $$ (a) The rate law for this reaction is first order in \(\mathrm{H}_{2}\) and second order in NO. Write the rate law. \((\mathbf{b})\) If the rate constant for this reaction at \(1000 \mathrm{~K}\) is $6.0 \times 10^{4} \mathrm{M}^{-2} \mathrm{~s}^{-1}\(, what is the reaction rate when \)[\mathrm{NO}]=0.035 \mathrm{M}\( and \)\left[\mathrm{H}_{2}\right]=0.015 \mathrm{M} ?(\mathbf{c})$ What is the reaction rate at \(1000 \mathrm{~K}\) when the concentration of \(\mathrm{NO}\) is increased to \(0.10 \mathrm{M},\) while the concentration of \(\mathrm{H}_{2}\) is \(0.010 \mathrm{M} ?\) (d) What is the reaction rate at \(1000 \mathrm{~K}\) if \([\mathrm{NO}]\) is decreased to \(0.010 \mathrm{M}\) and \(\left[\mathrm{H}_{2}\right]\) is increased to \(0.030 \mathrm{M} ?\)

The rate of the reaction $4 \mathrm{PH}_{3}(g) \rightarrow \mathrm{P}_{4}(g)+6 \mathrm{H}_{2}(g)\( was studied by charging \)\mathrm{PH}_{3}(g)$ into a constant-volume reaction vessel and measuring the total pressure.

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