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(a) A compound with formula \(\mathrm{RuCl}_{3} \cdot 5 \mathrm{H}_{2} \mathrm{O}\) is dissolved in water, forming a solution that is approximately the same color as the solid. Immediately after forming the solution, the addition of excess \(\mathrm{AgNO}_{3}(a q)\) forms 2 mol of solid \(\mathrm{AgCl}\) per mole of complex. Write the formula for the compound, showing which ligands are likely to be present in the coordination sphere. (b) After a solution of \(\mathrm{RuCl}_{3} \cdot 5 \mathrm{H}_{2} \mathrm{O}\) has stood for about a year, addition of \(\mathrm{AgNO}_{3}(a q)\) precipitates 3 mol of AgCl per mole of complex. What has happened in the ensuing time?

Short Answer

Expert verified
The initial complex formula is \([\mathrm{RuCl}_{2}(\mathrm{H}_{2}\mathrm{O})_{2}]Cl\cdot 3\mathrm{H}_{2}\mathrm{O}\) after the immediate reaction with \(\mathrm{AgNO}_{3}\). After standing for about a year, the complex formula changes to \([\mathrm{RuCl}_{3}(\mathrm{H}_{2}\mathrm{O})]Cl_{2}\cdot 4\mathrm{H}_{2}\mathrm{O}\) due to the replacement of a water ligand by a Cl atom in the coordination sphere.

Step by step solution

01

Analyze the immediate reaction with AgNO3

The initial compound has the formula \(\mathrm{RuCl}_{3} \cdot 5 \mathrm{H}_{2} \mathrm{O}\). When the compound is dissolved in water and reacts with an excess of AgNO3, it forms 2 moles of solid \(\mathrm{AgCl}\) per mole of complex. Based on this information, we can infer that there are 2 Cl atoms in the coordination sphere of the Ru complex.
02

Propose the complex formula after initial reaction with AgNO3

Since two of the Cl atoms in the original compound \(\mathrm{RuCl}_{3} \cdot 5 \mathrm{H}_{2} \mathrm{O}\) are coordinated to the Ru atom, we can propose the complex formula to be: \([\mathrm{RuCl}_{2}(\mathrm{H}_{2}\mathrm{O})_{2}]Cl\cdot 3\mathrm{H}_{2}\mathrm{O}\).
03

Analyze the reaction after a year of standing

After the solution has stood for about a year, we are informed that the addition of \(\mathrm{AgNO}_{3}(a q)\) precipitates 3 moles of \(\mathrm{AgCl}\) per mole of complex. This information suggests that an additional Cl atom in the coordination sphere of the Ru complex has been replaced.
04

Determine the change in the coordination sphere

We infer that a water ligand in the coordination sphere has been replaced by a Cl atom, as the number of moles of \(\mathrm{AgCl}\) precipitated has increased. The coordination sphere of the complex after this change will contain 3 Cl atoms instead of 2.
05

Propose the final complex formula

Accounting for the change in the coordination sphere of the Ru complex, we can now propose the complex formula to be: \([\mathrm{RuCl}_{3}(\mathrm{H}_{2}\mathrm{O})]Cl_{2}\cdot 4\mathrm{H}_{2}\mathrm{O}\). This is the formula of the complex after it has stood for about a year and then reacted with \(\mathrm{AgNO}_{3}(a q)\).

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Complex Ions
In coordination chemistry, a complex ion consists of a central metal atom or ion that is bonded to surrounding molecules or ions—these are known as ligands. The central metal and the ligands together form a coordination entity, which can carry a charge, thus forming a complex ion. This charge can be positive, negative, or neutral, depending on the charge of the central metal and the nature of the ligands present.
Moreover, the metal and ligands are bonded via coordinate covalent bonds, where the ligands donate electron pairs to the metal ion.
Understanding these complex ions is crucial, as they are found in many biological systems, such as hemoglobin in blood, and play significant roles in various chemical reactions.
Ligand Exchange
Ligand exchange is the process where one or more ligands in a coordination complex are replaced by different ligands. This exchange can occur for various reasons, such as changes in the concentration of the surrounding solution or over time due to thermodynamic stability.
  • In our example, initially, the coordination sphere of the complex had two chloride ligands with two water molecules.
  • As time progressed, one water ligand was replaced by a chloride ion, increasing the number of replaceable chloride ions in the solution.
This is an important reaction mechanism in coordination chemistry, as it affects the color, reactivity, and solubility of the complex ion.
Coordination Sphere
The coordination sphere consists of the central metal ion and the surrounding attached ligands. In a chemical formula, the coordination sphere is indicated using square brackets, such as in \( [\text{RuCl}_2(\text{H}_2\text{O})_2] \).
This represents the part of the complex where direct bonding interactions occur. The coordination sphere defines the geometry and coordination number (the number of direct bonds to the metal center) of the complex.
  • In the original exercise, the coordination sphere contained two chloride ions and two water molecules.
  • With time, changes in the coordination sphere were observed, featuring a transition to three chloride ions and one water molecule.
These changes dramatically impact the properties of the compound, illustrating the dynamic nature of coordination chemistry.

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Most popular questions from this chapter

The complex \(\left[\mathrm{Mn}\left(\mathrm{NH}_{3}\right)_{6}\right]^{2+}\) contains five unpaired electrons. Sketch the energy-level diagram for the \(d\) orbitals, and indicate the placement of electrons for this complex ion. Is the ion a high-spin or a low-spin complex?

(a) Using Werner's definition of valence, which property is the same as oxidation number, primary valence or secondary valence? (b) What term do we normally use for the other type of valence? (c) Why can \(\mathrm{NH}_{3}\) serve as a ligand but \(\mathrm{BH}_{3}\) cannot?

Metallic elements are essential components of many important enzymes operating within our bodies. Carbonic anhydrase, which contains \(\mathrm{Zn}^{2+}\) in its active site, is responsible for rapidly interconverting dissolved \(\mathrm{CO}_{2}\) and bicarbonate ion, \(\mathrm{HCO}_{3}^{-}\). The zinc in carbonic anhydrase is tetrahedrally coordinated by three neutral nitrogencontaining groups and a water molecule. The coordinated water molecule has a \(\mathrm{p} K_{a}\) of \(7.5,\) which is crucial for the enzyme's activity. (a) Draw the active site geometry for the \(\mathrm{Zn}(\mathrm{II})\) center in carbonic anhydrase, just writing "N" for the three neutral nitrogen ligands from the protein. (b) Compare the \(\mathrm{p} K_{a}\) of carbonic anhydrase's active site with that of pure water; which species is more acidic? (c) When the coordinated water to the \(\mathrm{Zn}(\mathrm{II})\) center in carbonic anhydrase is deprotonated, what ligands are bound to the \(\mathrm{Zn}(\mathrm{II})\) center? Assume the three nitrogen ligands are unaffected. \((\mathbf{d})\) The \(\mathrm{p} K_{a}\) of \(\left[\mathrm{Zn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+}\) is \(10 .\) Suggest an explanation for the difference between this \(\mathrm{p} K_{a}\) and that of carbonic anhydrase. (e) Would you expect carbonic anhydrase to have a deep color, like hemoglobin and other metal-ion-containing proteins do? Explain.

The ion \(\left[\mathrm{Fe}(\mathrm{CN})_{6}\right]^{3-}\) has one unpaired electron, whereas \(\left[\mathrm{Fe}(\mathrm{NCS})_{6}\right]^{3-}\) has five unpaired electrons. From these results, what can you conclude about whether each complex is high spin or low spin? What can you say about the placement of \(\mathrm{NCS}^{-}\) in the spectrochemical series?

The molecule dimethylphosphinoethane \(\left[\left(\mathrm{CH}_{3}\right)_{2} \mathrm{PCH}_{2} \mathrm{CH}_{2}\right.\) \(\mathrm{P}\left(\mathrm{CH}_{3}\right)_{2},\) which is abbreviated dmpe] is used as a ligand for some complexes that serve as catalysts. A complex that contains this ligand is \(\mathrm{Mo}(\mathrm{CO})_{4}(\) dmpe \()\). (a) Draw the Lewis structure for dmpe, and compare it with ethylenediamine as a coordinating ligand. (b) What is the oxidation state of Mo in \(\mathrm{Na}_{2}\left[\mathrm{Mo}(\mathrm{CN})_{2}(\mathrm{CO})_{2}(\) dmpe \()\right] ?(\mathbf{c})\) Sketch the structure of the \(\left[\mathrm{Mo}(\mathrm{CN})_{2}(\mathrm{CO})_{2}(\text { dmpe })\right]^{2-}\) ion, including all the possible isomers.

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