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Passage Living Organisms That Require Oxygen to Respire Can Build Up

Question 259

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Passage
Living organisms that require oxygen to respire can build up hydrogen peroxide (H2O2) as a byproduct of respiration.  Because hydrogen peroxide can cause oxidative damage to cells, the amount of H2O2 in cells must be closely regulated.  Although H2O2 decomposes spontaneously, a catalyst is needed for the reaction to occur at a sufficiently rapid rate suitable for biological purposes.  In biological systems, an enzyme called a catalase accelerates the catalytic decomposition of H2O2 into water and oxygen (Reaction 1) .
Passage Living organisms that require oxygen to respire can build up hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>)  as a byproduct of respiration.  Because hydrogen peroxide can cause oxidative damage to cells, the amount of H<sub>2</sub>O<sub>2</sub> in cells must be closely regulated.  Although H<sub>2</sub>O<sub>2</sub> decomposes spontaneously, a catalyst is needed for the reaction to occur at a sufficiently rapid rate suitable for biological purposes.  In biological systems, an enzyme called a catalase accelerates the catalytic decomposition of H<sub>2</sub>O<sub>2</sub> into water and oxygen (Reaction 1) .    <strong>Reaction 1</strong>In a laboratory setting, several different inorganic compounds can also serve as catalysts for H<sub>2</sub>O<sub>2</sub> decomposition, allowing researchers to compare how different catalysts affect the efficiency of the reaction.  To compare Fe(NO<sub>3</sub>) <sub>3</sub> (a metal homogeneous catalyst)  and NaI (a halogen homogeneous catalyst) , researchers measured the amount of heat evolved after placing each catalyst in a fresh solution of 3% hydrogen peroxide.To perform the measurements, the researchers placed 50 mL of 3% H<sub>2</sub>O<sub>2</sub> in an insulated coffee cup to be used as a calorimeter, as shown in Figure 1.  Before adding any catalyst, the initial, baseline temperature of the H<sub>2</sub>O<sub>2</sub> solution was determined by recording the temperature every 30 seconds for 5 minutes.  Then 10 mL of 0.10 M Fe(NO<sub>3</sub>) <sub>3</sub>(aq)  catalyst was added to the H<sub>2</sub>O<sub>2</sub> solution.  The temperature was recorded every 30 seconds for another 15 minutes.  The experiment was then repeated using 10 mL of 0.50 M sodium iodide in 0.01 M NaOH as the catalyst.  The results for each reaction are shown in Figure 2.    <strong>Figure 1</strong>  Coffee cup calorimeter    <strong>Figure 2</strong>  Temperature vs. time measurements for reactions catalyzed by Fe(NO<sub>3</sub>) <sub>3</sub> and NaI Adapted from: C. Marzzacco,  The effect of a change in catalyst on the enthalpy of decomposition of hydrogen peroxide.  Chem13 News Magazine. ©2008 University of Waterloo. -The experiment was repeated with 3.0 g of solid MnO<sub>2</sub> particles added as an alternative catalyst.  When MnO<sub>2</sub> was ground to a fine powder, the temperature rose more quickly than when the particles were not ground.  The most likely reason for this is that with heterogeneous catalysts: A) the rate increases when the catalyst is oxidized. B) the rate increases as the catalyst surface area is increased. C) the rate decreases due to competing side reactions. D) the rate decreases when the catalyst is insoluble. Reaction 1In a laboratory setting, several different inorganic compounds can also serve as catalysts for H2O2 decomposition, allowing researchers to compare how different catalysts affect the efficiency of the reaction.  To compare Fe(NO3) 3 (a metal homogeneous catalyst) and NaI (a halogen homogeneous catalyst) , researchers measured the amount of heat evolved after placing each catalyst in a fresh solution of 3% hydrogen peroxide.To perform the measurements, the researchers placed 50 mL of 3% H2O2 in an insulated coffee cup to be used as a calorimeter, as shown in Figure 1.  Before adding any catalyst, the initial, baseline temperature of the H2O2 solution was determined by recording the temperature every 30 seconds for 5 minutes.  Then 10 mL of 0.10 M Fe(NO3) 3(aq) catalyst was added to the H2O2 solution.  The temperature was recorded every 30 seconds for another 15 minutes.  The experiment was then repeated using 10 mL of 0.50 M sodium iodide in 0.01 M NaOH as the catalyst.  The results for each reaction are shown in Figure 2.
Passage Living organisms that require oxygen to respire can build up hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>)  as a byproduct of respiration.  Because hydrogen peroxide can cause oxidative damage to cells, the amount of H<sub>2</sub>O<sub>2</sub> in cells must be closely regulated.  Although H<sub>2</sub>O<sub>2</sub> decomposes spontaneously, a catalyst is needed for the reaction to occur at a sufficiently rapid rate suitable for biological purposes.  In biological systems, an enzyme called a catalase accelerates the catalytic decomposition of H<sub>2</sub>O<sub>2</sub> into water and oxygen (Reaction 1) .    <strong>Reaction 1</strong>In a laboratory setting, several different inorganic compounds can also serve as catalysts for H<sub>2</sub>O<sub>2</sub> decomposition, allowing researchers to compare how different catalysts affect the efficiency of the reaction.  To compare Fe(NO<sub>3</sub>) <sub>3</sub> (a metal homogeneous catalyst)  and NaI (a halogen homogeneous catalyst) , researchers measured the amount of heat evolved after placing each catalyst in a fresh solution of 3% hydrogen peroxide.To perform the measurements, the researchers placed 50 mL of 3% H<sub>2</sub>O<sub>2</sub> in an insulated coffee cup to be used as a calorimeter, as shown in Figure 1.  Before adding any catalyst, the initial, baseline temperature of the H<sub>2</sub>O<sub>2</sub> solution was determined by recording the temperature every 30 seconds for 5 minutes.  Then 10 mL of 0.10 M Fe(NO<sub>3</sub>) <sub>3</sub>(aq)  catalyst was added to the H<sub>2</sub>O<sub>2</sub> solution.  The temperature was recorded every 30 seconds for another 15 minutes.  The experiment was then repeated using 10 mL of 0.50 M sodium iodide in 0.01 M NaOH as the catalyst.  The results for each reaction are shown in Figure 2.    <strong>Figure 1</strong>  Coffee cup calorimeter    <strong>Figure 2</strong>  Temperature vs. time measurements for reactions catalyzed by Fe(NO<sub>3</sub>) <sub>3</sub> and NaI Adapted from: C. Marzzacco,  The effect of a change in catalyst on the enthalpy of decomposition of hydrogen peroxide.  Chem13 News Magazine. ©2008 University of Waterloo. -The experiment was repeated with 3.0 g of solid MnO<sub>2</sub> particles added as an alternative catalyst.  When MnO<sub>2</sub> was ground to a fine powder, the temperature rose more quickly than when the particles were not ground.  The most likely reason for this is that with heterogeneous catalysts: A) the rate increases when the catalyst is oxidized. B) the rate increases as the catalyst surface area is increased. C) the rate decreases due to competing side reactions. D) the rate decreases when the catalyst is insoluble. Figure 1  Coffee cup calorimeter
Passage Living organisms that require oxygen to respire can build up hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>)  as a byproduct of respiration.  Because hydrogen peroxide can cause oxidative damage to cells, the amount of H<sub>2</sub>O<sub>2</sub> in cells must be closely regulated.  Although H<sub>2</sub>O<sub>2</sub> decomposes spontaneously, a catalyst is needed for the reaction to occur at a sufficiently rapid rate suitable for biological purposes.  In biological systems, an enzyme called a catalase accelerates the catalytic decomposition of H<sub>2</sub>O<sub>2</sub> into water and oxygen (Reaction 1) .    <strong>Reaction 1</strong>In a laboratory setting, several different inorganic compounds can also serve as catalysts for H<sub>2</sub>O<sub>2</sub> decomposition, allowing researchers to compare how different catalysts affect the efficiency of the reaction.  To compare Fe(NO<sub>3</sub>) <sub>3</sub> (a metal homogeneous catalyst)  and NaI (a halogen homogeneous catalyst) , researchers measured the amount of heat evolved after placing each catalyst in a fresh solution of 3% hydrogen peroxide.To perform the measurements, the researchers placed 50 mL of 3% H<sub>2</sub>O<sub>2</sub> in an insulated coffee cup to be used as a calorimeter, as shown in Figure 1.  Before adding any catalyst, the initial, baseline temperature of the H<sub>2</sub>O<sub>2</sub> solution was determined by recording the temperature every 30 seconds for 5 minutes.  Then 10 mL of 0.10 M Fe(NO<sub>3</sub>) <sub>3</sub>(aq)  catalyst was added to the H<sub>2</sub>O<sub>2</sub> solution.  The temperature was recorded every 30 seconds for another 15 minutes.  The experiment was then repeated using 10 mL of 0.50 M sodium iodide in 0.01 M NaOH as the catalyst.  The results for each reaction are shown in Figure 2.    <strong>Figure 1</strong>  Coffee cup calorimeter    <strong>Figure 2</strong>  Temperature vs. time measurements for reactions catalyzed by Fe(NO<sub>3</sub>) <sub>3</sub> and NaI Adapted from: C. Marzzacco,  The effect of a change in catalyst on the enthalpy of decomposition of hydrogen peroxide.  Chem13 News Magazine. ©2008 University of Waterloo. -The experiment was repeated with 3.0 g of solid MnO<sub>2</sub> particles added as an alternative catalyst.  When MnO<sub>2</sub> was ground to a fine powder, the temperature rose more quickly than when the particles were not ground.  The most likely reason for this is that with heterogeneous catalysts: A) the rate increases when the catalyst is oxidized. B) the rate increases as the catalyst surface area is increased. C) the rate decreases due to competing side reactions. D) the rate decreases when the catalyst is insoluble. Figure 2  Temperature vs. time measurements for reactions catalyzed by Fe(NO3) 3 and NaI
Adapted from: C. Marzzacco, "The effect of a change in catalyst on the enthalpy of decomposition of hydrogen peroxide." Chem13 News Magazine. ©2008 University of Waterloo.
-The experiment was repeated with 3.0 g of solid MnO2 particles added as an alternative catalyst.  When MnO2 was ground to a fine powder, the temperature rose more quickly than when the particles were not ground.  The most likely reason for this is that with heterogeneous catalysts:


A) the rate increases when the catalyst is oxidized.
B) the rate increases as the catalyst surface area is increased.
C) the rate decreases due to competing side reactions.
D) the rate decreases when the catalyst is insoluble.

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