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The following data were obtained for the gas-phase decomposition of di nitrogen pentoxide,

2N2O5(g)4NO2(g)+O2(g)

[N2O5]0(mol/L)

Initial Rate(molL-1s-1)


0.0750

8.90×10-4

0.190

2.26×10-3

0.275

3.26×10-3

0.410

4.85×10-3

Where,Rate=-d[N2O5]dt

Write the rate law and calculate the value of the rate constant.

Short Answer

Expert verified

Rate=kN2O5

The value of the rate constant will bekmean=1.19×10-2s-1.

Step by step solution

01

Write the rate laws for the first 2 experiments

It is given that

Rate=-dN2O5dtRate=kN2O5x

For the 1st two experiments:

8.90×10-4=k0.0750x......12.26×10-3=k0.190x......2

Dividing (2) by (1), we get

2.54=0.1900.0750x2.54=2.53xx1

So, the rate of the reaction will be given by:

Rate=kN2O5x=kN2O5

02

Now calculate the rate constant.

Rate=kN2O5x

k=RateN2O5=8.90×10-4molL-1s-10.0750mol/L

(From experiment 1)

So,k=1.19×10-2s-1

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Most popular questions from this chapter

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.

What two requirements must be met to call a mechanism plausible? Why say a “plausible” mechanism instead of the correct mechanism? Is it true that most reactions occur by a one-step mechanism? Explain.

How is the rate of a reaction affected by each of the following?

(a)Activation energy

(b)Temperature

(c) Frequency of collisions

(d) Orientation of collisions

The rate of the reaction between haemoglobin (Hb)and carbon monoxide (CO)was studied at20oC. The following data were collected, with all concentration units inμmol/L. (A haemoglobin concentration of2.21μmol/L is equal to2.21×10-6mol/L.)

[Hb]0(μmol/L)
[CO]0(μmol/L)
Initial Rate(μmolL-1s-1)
2.211.000.619
4.421.001.24
4.423.003.71

a. Determine the orders of this reaction with respect to Hb and CO.

b. Determine the rate law.

c. Calculate the value of the rate constant.

d. What would be the initial rate for an experiment withlocalid="1663765857044" [Hb]0=36μmol/Landlocalid="1663764418756" [CO]0=2.40μmol/L.

The decomposition of NH3 to N2 and H2 was studied on

two surfaces:

Without a catalyst, the activation energy is 335 kJ/mol.

a. Which surface is the better heterogeneous catalystfor the decomposition of NH3? Why?

b. How many times faster is the reaction at 298 K onthe W surface compared with the reaction with nocatalyst present? Assume that the frequency factor A

is the same for each reaction.

c. The decomposition reaction on the two surfacesobeys a rate law of the form

Rate=KNH3H2

How can you explain the inverse dependence of therate on the H2 concentration?

See all solutions

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