
An excellent way to make highly pure nickel metal for use in specialized steel alloys is to decompose Ni(CO)4 by heating it in a vacuum to slightly above room temperature.
Ni(CO)4(g) → Ni(s) + 4 CO(g)
The reaction is proposed to occur in four steps, the first of which is
Ni(CO)4(g) → Ni(CO)3(g) + CO(g)
Kinetic studies of this first-order decomposition reaction have been carried out between 47.3 °C and 66.0 °C to give the results in the table.*
- (a) Determine the activation energy for this reaction.
- (b) Ni(CO)4 is formed by the reaction of nickel metal with carbon monoxide. Suppose that 2.05 g CO is combined with 0.125 g nickel metal. Determine the maximum mass (g) of Ni(CO)4 that can be formed.
Replacement of CO by another molecule in Ni(CO)4 was studied in the nonaqueous solvents toluene and hexane to understand the general principles that govern the chemistry of such compounds.*
Ni(CO)4(g) + P(CH3)3 → Ni(CO)3P(CH3)3 + CO
A detailed study of the kinetics of the reaction led to the mechanism
- (c) Which step in the mechanism is unimolecular? Which is bimolecular?
- (d) Add the steps of the mechanism to show that the result is the balanced equation for the observed reaction.
- (e) Is there an intermediate in this reaction? If so, what is it?
- (f) It was found that doubling the concentration of Ni(CO)4 increased the reaction rate by a factor of 2. Doubling the concentration of P(CH3)3 had no effect on the reaction rate. Based on this information, write the rate equation for the reaction.
- (g) Does the experimental rate equation support the proposed mechanism? Why or why not?
(a)

Interpretation:
The activation energy of the reaction has to be determined. The reaction is given below.
Concept Introduction:
The Arrhenius equation is given below.
Where,
By taking
The above equation is in the form of
Explanation of Solution
A table has to be made as shown below by using the given data.
A graph can be plotted as
Figure
From the slope of the above graph, the activation energy of the reaction can be calculated.
Therefore, the activation energy of the reaction is
(b)

Interpretation:
The maximum mass
Explanation of Solution
The reverse reaction of the given reaction represents the formation of
Four moles of
Determination of limiting reagent:
The number of
The mass of
Therefore, the maximum mass
(c)

Interpretation:
The unimolecular and bimolecular step have to be chosen from the given mechanism.
Explanation of Solution
A reaction is called as elementary and unimolecular reaction if the reaction involves only one reactant. If the reaction has exactly two reactants, either two of the same reactants or one of each of different reactants, then the reaction is bimolecular and elementary.
The first step is unimolecular as it involves exactly one reactant. The second step is bimolecular as it involves exactly two reactants.
(d)

Interpretation:
The steps of the given mechanism has to be added in order to show that the result is the balanced equation for the observed reaction.
Explanation of Solution
The given mechanisms can be added as given below.
The resulting equation is the same as that given for the observed reaction.
(e)

Interpretation:
The intermediate involved in the reaction has to be determined.
Explanation of Solution
An intermediate is a chemical substance that is generated in an early step of a reaction and then used up in a later step. In the given mechanism, the intermediate is
(f)

Interpretation:
Doubling the concentration of
Explanation of Solution
The reaction is given below.
Suppose the rate of the above reaction is as follows,
Where,
Given that, doubling the concentration of
The second condition is doubling the concentration of
Now, the rate equation can be written as shown below.
(g)

Interpretation:
The experimental rate equation support the proposed mechanism or not, has to be explained. The mechanism is given below.
Explanation of Solution
The experimental rate equation can be written as shown below.
The slowest step in a mechanism is the rate determining step. Thus, according to the mechanism, the rate determining step is the first step. The rate equation can be written as follows,
Thus, the experimental rate equation supports the proposed mechanism.
Want to see more full solutions like this?
Chapter 11 Solutions
Chemistry: The Molecular Science
- Draw the a-anomer cyclized pyranose Haworth projection of the below hexose. Circle the anomeric carbons. Number the carbons on the Fischer and Haworth projections. Assign R and S for each chiral center. HO CHO -H HO -H H- -OH H -OH CH₂OH Draw the ẞ-anomer cyclized furanose Haworth projection for the below hexose. Circle the anomeric carbons. Number the carbons on the Fischer and Haworth projections. HO CHO -H H -OH HO -H H -OH CH₂OHarrow_forwardName the below disaccharide. Circle any hemiacetals. Identify the numbering of glycosidic linkage, and identify it as a or ẞ. OH HO HO OH HO HO HO OHarrow_forwardWhat are the monomers used to make the following polymers? F. а. b. с. d. Вецер хочому なarrow_forward
- 1. Propose a reasonable mechanism for the following transformation. I'm looking for curved mechanistic arrows and appropriate formal charges on intermediates. OMe MeO OMe Me2N NMe2 OTBS OH xylenes OMe 'OTBSarrow_forwardWhat is the polymer made from the following monomers? What type of polymerization is used for each? а. ОН H2N но b. ن -NH2 d. H₂N NH2 довarrow_forwardCondensation polymers are produced when monomers containing two different functional groups link together with the loss of a small molecule such as H2O. The difunctional monomer H2N(CH2)6COOH forms a condensation polymer. Draw the carbon-skeleton structure of the dimer that forms from this monomer.arrow_forward
- What is the structure of the monomer?arrow_forward→ BINDERIYA GANBO... BINDERIYA GANBO. AP Biology Notes Gamino acid chart - G... 36:22 司 10 ☐ Mark for Review Q 1 Hide 80 8 2 =HA O=A¯ = H₂O Acid HIO HBrO HCIO Question 10 of 35 ^ Σ DELL □ 3 % Λ & 6 7 * ∞ 8 do 5 $ 4 # m 3 ° ( 9 Highlights & Notes AXC Sign out Carrow_forwardWhich representation(s) show polymer structures that are likely to result in rigid, hard materials and those that are likely to result in flexible, stretchable, soft materials?arrow_forward
- 3. Enter the molecular weight of the product obtained from the Williamson Ether Synthesis? OH OH & OH excess CH3l Ag₂Oarrow_forwardPlease answer 1, 2 and 3 on the endarrow_forwardIn the box below, specify which of the given compounds are very soluble in polar aprotic solvents. You may select more than one compound. Choose one or more: NaCl NH4Cl CH3CH2CH2CH2CH2CN CH3CH2OH hexan-2-one NaOH CH3SCH3arrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- Chemistry for Engineering StudentsChemistryISBN:9781337398909Author:Lawrence S. Brown, Tom HolmePublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning





