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Would the slope of a ln(k) versus 1/T (K) plot for a catalyzed reaction be more or less negative than the slope of a ln(k) versus 1/T (K) plot for the uncatalyzed reaction? Assume that both rate laws are first-order. Explain

Short Answer

Expert verified

For the catalyzed reaction has a less negative slope than the uncatalyzed reaction. In catalysis, the reduction in the activation energy potential expresses that the reaction is catalyzed by catalysts.

Step by step solution

01

Explaining the Arrhenius equation and collision theory

The collision theory states that the particles of the substrate are assumed to be spheres colliding with other particles of the substrate with a specific orientation and minimum energy, which results in the formation of products.

The Arrhenius equation is the relationship between the temperature and rate constant of reaction (k) based on the collision theory. The rate constant depends upon the collision factor, activation energy, and temperature.

The Arrhenius equation is as follows –

k=Ae-ERT

Where k is the reaction rate constant,

A is Arrhenius or collision factor,

E is the activation energy in kJ/mol,

R is gas constant,

T is the temperature in K.

02

Explain the role of the catalyst in the catalyzed and uncatalyzed reactions using the Arrhenius equation.

The catalyst is necessary for the reaction to proceed by lowering the activation energy in acatalyzed reaction. During the uncatalyzed reaction, the activation energy is not reduced.

The reaction is favorable if the reactant molecules overtake the activation energy barrier for catalyzed reactions. If the energy barrier is minimized, the rate is increased.

Therefore, in the Arrhenius equation, ERTterm should be minimum for a larger rate constant. As increases in the term, the exponential value will be more in the denominator which leads to the rate constantk decreases and vice-versa.

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Most popular questions from this chapter

A friend of yours states, “A balanced equation tells us how chemicals interact. Therefore, we can determine the rate law directly from the balanced equation.” What do you tell your friend?

Describe at least two experiments you could perform to determine a rate law.

The following data were obtained for the reaction

2ClO2(aq)+2OH-(aq)ClO3-(aq)+ClO2(aq)+H2O(I)

Where,Rate=-d[ClO2]dt

[ClO2]0(mol/L)

role="math" localid="1663766560289" [OH-]0(mol/L)

Initial Rate

(molL-1s-1)

0.0500

0.100

5.75×10-2

0.100

0.100

2.30×10-1

0.100

0.0500

1.15×10-1

a. Determine the rate law and the value of the rate constant.

b. What would be the initial rate for an experiment with[ClO2]0=0.175mol/Land[OH-]0=0.0844mol/L?

Write the rate laws of the following elementary reactions.

(a)CH3NC(g)CH3CN(g)(b)O3(g)+NO(g)O2(g)+NO2(g)(C)O3(g)O2+O(g)(d)O3(g)+O(g)2O2(g)(e)C614N714+βparticle(nucleardecay)

Consider the hypothetical reaction

BE+F

which is assumed to occur by the mechanism

B+BK-1K1B*+BB*K2E+F

where B*represents a Bmolecule with enough energy to surmount the reaction energy barrier.

(a) Derive the rate law for the production of Eusing the steady-state approximation.

(b) Assume that this condition is known to be first order. Under what conditions does your derived rate law (from part a) agree with this observation.

(c) Explain how a chemical reaction can be first order, since even in a simple case (BE+F)molecules must collide to build up enough energy to get over the energy barrier. Why aren’t all reactions at least second order ? In other words, explain the physical significance of the result from part b.

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