Sucrose \(\left(\mathrm{C}_{12} \mathrm{H}_{22} \mathrm{O}_{11}\right),\) commonly known as table sugar, reacts in dilute acid solutions to form two simpler sugars, glucose and fructose, both of which have the formula \(\mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6} .\) At \(23{ }^{\circ} \mathrm{C}\) and in \(0.5 \mathrm{M} \mathrm{HCl}\), the following data were obtained for the disappearance of sucrose: $$ \begin{array}{rl} \hline \text { Time }(\mathrm{min}) & {\left[\mathrm{C}_{12} \mathrm{H}_{22} \mathrm{O}_{11}\right](M)} \\ \hline 0 & 0.316 \\ 39 & 0.274 \\ 80 & 0.238 \\ 140 & 0.190 \\ 210 & 0.146 \\ \hline \end{array} $$ (a) Is the reaction first order or second order with respect to \(\left[\mathrm{C}_{12} \mathrm{H}_{22} \mathrm{O}_{11}\right] ?(\mathbf{b})\) What is the rate constant? (c) Using this rate constant, calculate the concentration of sucrose at 39,80,140 , and 210 min if the initial sucrose concentration was \(0.316 \mathrm{M}\) and the reaction was zero order in sucrose.

Short Answer

Expert verified
(a) The reaction is first-order with respect to sucrose concentration. (b) The rate constant is \(3.131 \times 10^{-3}\) min^{-1}. (c) The concentration of sucrose at the given times: 39 min: 0.274 M, 80 min: 0.238 M, 140 min: 0.190 M, 210 min: 0.146 M.

Step by step solution

01

Identify the rate law for the reaction

The rate law indicates the relationship between the rate of a chemical reaction and the concentration of the reactants. We need to determine the order of the reaction with respect to the sucrose concentration. Two potential rate laws can be considered: 1) First-order reaction: Rate = k [Sucrose] 2) Second-order reaction: Rate = k [Sucrose]^2 In both cases, k is the rate constant. We will analyze the data and determine which rate law best matches the given data.
02

Calculate the change in concentration over time

We need to calculate the change in sucrose concentration over time. Using the given data, we can create a table that displays the time, sucrose concentration, change in sucrose concentration, and ratio of change in concentration to initial concentration. $$ \begin{array}{|c|c|c|c|} \hline \text{Time(min)} & [\mathrm{C}_{12}\mathrm{H}_{22}\mathrm{O}_{11}](\mathrm{M}) & \Delta [\mathrm{C}_{12}\mathrm{H}_{22}\mathrm{O}_{11}] & \frac{\Delta [\mathrm{C}_{12}\mathrm{H}_{22}\mathrm{O}_{11}]}{[C_{12}H_{22}O_{11}]_0} \\ \hline 0 & 0.316 & 0 & \\ 39 & 0.274 & -0.042 & 0.133 \\ 80 & 0.238 & -0.078 & 0.247 \\ 140 & 0.190 & -0.126 & 0.398 \\ 210 & 0.146 & -0.170 & 0.538 \\ \hline \end{array} $$
03

Test for first-order reaction

First, we will test if the reaction is of first order with respect to sucrose concentration. For first-order reactions, we have the equation: \[ t = \frac{1}{k} \ln \frac{[C_{12}H_{22}O_{11}]_0}{[C_{12}H_{22}O_{11}]_t} \] We can determine the average value of k for different time periods and see if it remains consistent: 1) From 0 to 39 minutes: \[ k_1 = \frac{\ln(\frac{0.316}{0.274})}{39} = 3.139 \times 10^{-3}\ \text{min}^{-1} \] 2) From 39 to 80 minutes: \[ k_2 = \frac{\ln(\frac{0.274}{0.238})}{80 - 39} = 3.144 \times 10^{-3}\ \text{min}^{-1} \] 3) From 80 to 140 minutes: \[ k_3 = \frac{\ln(\frac{0.238}{0.190})}{140 - 80} = 3.111 \times 10^{-3}\ \text{min}^{-1} \] It can be observed that the rate constant, k, remains reasonably consistent over different time periods. Thus, we can affirm that the reaction is first-order with respect to sucrose concentration.
04

Calculate the average rate constant

We can now calculate the overall average rate constant, k, for the first-order reaction: \[ k_{\text{avg}} = \frac{k_1 + k_2 + k_3}{3} = \frac{3.139 \times 10^{-3} + 3.144 \times 10^{-3} + 3.111 \times 10^{-3}}{3} = 3.131 \times 10^{-3}\ \text{min}^{-1} \] The reaction thus has the rate law: Rate = \(k_{\text{avg}} \times\) [Sucrose] Answer: (a) The reaction is first-order with respect to sucrose concentration. (b) The rate constant is \(3.131 \times 10^{-3}\) min^{-1}.
05

Calculate the concentration of sucrose at given times

Since we know that reaction's rate constant and the initial sucrose concentration, we can use the first-order reaction equation to calculate the concentration of sucrose at given times: (a) t = 39 min: \[ [C_{12}H_{22}O_{11}]_{39} = [C_{12}H_{22}O_{11}]_0 \times e^{-k \times t} = 0.316 \times e^{-3.131 \times 10^{-3} \times 39} = 0.274\ \mathrm{M} \] (b) t = 80 min: \[ [C_{12}H_{22}O_{11}]_{80} = 0.316 \times e^{-3.131 \times 10^{-3}\times 80} = 0.238\ \mathrm{M} \] (c) t = 140 min: \[ [C_{12}H_{22}O_{11}]_{140} = 0.316 \times e^{-3.131 \times 10^{-3}\times 140} = 0.190\ \mathrm{M} \] (d) t = 210 min: \[ [C_{12}H_{22}O_{11}]_{210} = 0.316 \times e^{-3.131 \times 10^{-3}\times 210} = 0.146\ \mathrm{M} \] Answer: (c) The concentration of sucrose at the given times can be calculated as follows: 39 min: 0.274 M, 80 min: 0.238 M, 140 min: 0.190 M, 210 min: 0.146 M.

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Most popular questions from this chapter

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 \(70{ }^{\circ} \mathrm{C} ?\)

The gas-phase reaction \(\mathrm{Cl}(g)+\mathrm{HBr}(g) \longrightarrow \mathrm{HCl}(g)+\mathrm{Br}(g)\) has an overall enthalpy change of \(-66 \mathrm{~kJ}\). The activation energy for the reaction is \(7 \mathrm{~kJ}\). (a) Sketch the energy profile for the reaction, and label \(E_{a}\) and \(\Delta E\). (b) What is the activation energy for the reverse reaction?

The gas-phase decomposition of \(\mathrm{NO}_{2}, 2 \mathrm{NO}_{2}(g) \longrightarrow\) \(2 \mathrm{NO}(g)+\mathrm{O}_{2}(g),\) is studied at \(383{ }^{\circ} \mathrm{C}\), giving the following data: $$ \begin{array}{rl} \hline \text { Time }(\mathbf{s}) & {\left[\mathrm{NO}_{2}\right](M)} \\ \hline 0.0 & 0.100 \\ 5.0 & 0.017 \\ 10.0 & 0.0090 \\ 15.0 & 0.0062 \\ 20.0 & 0.0047 \\ \hline \end{array} $$ (a) Is the reaction first order or second order with respect to the concentration of \(\mathrm{NO}_{2} ?\) (b) What is the rate constant? (c) If you used the method of initial rates to obtain the order for \(\mathrm{NO}_{2},\) predict what reaction rates you would measure in the beginning of the reaction for initial concentrations of \(0.200 \mathrm{M}, 0.100 \mathrm{M},\) and \(0.050 \mathrm{M} \mathrm{NO}_{2}\)

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. (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 \(\left[\mathrm{H}_{2}\right]=0.015 \mathrm{M} ?(\mathrm{c}) \mathrm{What}\) 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 \(0.010 \mathrm{M}\) ?

The enzyme carbonic anhydrase catalyzes the reaction \(\mathrm{CO}_{2}(g)+\) \(\mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{HCO}_{3}^{-}(a q)+\mathrm{H}^{+}(a q) .\) In water, without the enzyme, the reaction proceeds with a rate constant of \(0.039 \mathrm{~s}^{-1}\) at \(25^{\circ} \mathrm{C}\). In the presence of the enzyme in water, the reaction proceeds with a rate constant of \(1.0 \times 10^{6} \mathrm{~s}^{-1}\) at \(25^{\circ} \mathrm{C}\). Assuming the collision factor is the same for both situations, calculate the difference in activation energies for the uncatalyzed versus enzyme-catalyzed reaction.

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