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Silicon-oxygen rings are a common structural feature in silicate chemistry. Draw the structure for the anion \(\left[\mathrm{Si}_{3} \mathrm{O}_{9}\right]^{6-},\) which is found in minerals such as benitoite. Is the ring expected to be planar?

Short Answer

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The \([\text{Si}_3\text{O}_9]^{6-}\) anion forms a planar ring with tetrahedral silicon coordination.

Step by step solution

01

Understanding the Composition of the Anion

The anion \([\text{Si}_3\text{O}_9]^{6-}\) contains three silicon (\(\text{Si}\)) atoms and nine oxygen (\(\text{O}\)) atoms. This anion forms a ring structure, with each silicon atom being tetrahedrally coordinated by oxygen atoms.
02

Drawing the Ring Structure

We start by arranging three silicon atoms in a triangular formation. Each silicon atom is connected to four oxygen atoms in a tetrahedral manner. However, for our planar ring, each silicon will share two of its oxygens with its neighboring silicons. These shared oxygens form the ring.
03

Accounting for Charge and Additional Oxygens

The remaining unshared oxygens complete each silicon's coordination. Since there are nine oxygens and three silicons, each silicon will have one 'non-bridging' oxygen, contributing to the overall 6- charge. The negative charge is delocalized over these non-bridging oxygens.
04

Examining Planarity of the Structure

The geometry around each silicon atom is tetrahedral, suggesting some distortion from perfect planarity. However, the ring's overall shape is nearly planar, typical of silicate ring structures due to the bonding angles and electrostatic repulsion in the formation.

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Key Concepts

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

Silicon-Oxygen Rings
Silicon-oxygen rings are an intriguing component of silicate chemistry, commonly seen in minerals such as benitoite. These rings are composed of alternating silicon (\(\text{Si}\)) and oxygen (\(\text{O}\)) atoms. When thinking about a silicon-oxygen ring like the anion \([ ext{Si}_3 ext{O}_9]^{6-}\), it's useful to visualize the structure as a closed loop. Each silicon atom in this type of ring bonds with four oxygen atoms, forming a tetrahedral shape around it.
  • Three silicon atoms are linked in a triangular pattern, making them form a ring with shared oxygens.
  • Shared oxygen atoms "bridge" the silicon atoms, while non-bridging oxygens contribute to the overall charge.
Understanding the connectivity in these silicon-oxygen rings can shed light on why these rings are stable and prevalent in nature. The electrostatic interactions balanced by sharing oxygen atoms help to maintain the integrity of these ring structures, allowing them to exist stably in various mineral forms.
Tetrahedral Coordination
In silicate chemistry, the concept of tetrahedral coordination is crucial, especially in understanding the structure of silicon-oxygen compounds. Each silicon atom in the ring such as \([ ext{Si}_3 ext{O}_9]^{6-}\) is surrounded by four oxygen atoms, forming a shape known as a tetrahedron. This is a three-dimensional shape where the silicon atom sits at the center, and the oxygen atoms occupy the corners.
  • Tetrahedral coordination results in strong covalent bonds between silicon and oxygen.
  • Oxygen atoms in a tetrahedron can sometimes be shared between adjacent silicon atoms, creating ring structures.
This arrangement provides structural stability due to the spatial orientation of the bonds. The angles and positions of these tetrahedrons help to explain the distortion from perfect planarity in silicon-oxygen rings in minerals. By sharing oxygen at their vertex, these tetrahedral units link together to form the intricate patterns found in silicate minerals.
Minerals
Minerals are naturally occurring substances with definitive chemical compositions and structures. In silicate minerals, the key component is the silicon-oxygen framework, which can form complex structures, including rings. The diversity of minerals is due in part to the ability of silicon and oxygen to form a wide variety of arrangements.
  • Silicate minerals, like benitoite, showcase different arrangements of silicon and oxygen.
  • These structures can range from isolated tetrahedrons to complex chains, sheets, and rings.
In the context of silicon-oxygen rings, minerals exhibit unique properties based on how these rings are assembled. This structural diversity results in various mineral characteristics, including hardness, color, and stability under environmental conditions. Each mineral's specific silicon-oxygen arrangement is a reflection of the geological processes that formed it.
Planarity of Structures
The planarity of structures, particularly in silicate rings like \([ ext{Si}_3 ext{O}_9]^{6-}\), is an important factor in understanding their behavior and properties. Although each silicon atom is tetrahedrally coordinated, which naturally introduces some three-dimensional contours, the overall arrangement of the ring tends towards planarity.
  • The nearly planar geometry results from interactions between the silicon and oxygen atoms aiming to minimize repulsion.
  • Planarity aids in the stacking and layering of these rings within minerals, influencing properties like cleavagability.
Despite slight deviations, these rings maintain a resemblance to a flat plane, enabling them to fit into layered mineral structures. This tendency towards planarity contributes to the stability of silicate minerals, as it allows for more extensive and complex interactions within the crystal lattice. The geometry and charge distribution within these rings further illustrate why they are both prevalent and essential in nature's mineral gallery.

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Most popular questions from this chapter

(a) Magnesium is obtained from sea water. If the concentration of \(\mathrm{Mg}^{2+}\) in sea water is \(0.050 \mathrm{M},\) what volume of sea water (in liters) must be treated to obtain \(1.00 \mathrm{kg}\) of magnesium metal? What mass of lime (CaO; in kilograms) must be used to precipitate the magnesium in this volume of sea water? (b) When \(1.2 \times 10^{3} \mathrm{kg}\) of molten \(\mathrm{MgCl}_{2}\) is electrolyzed to produce magnesium, what mass (in kilograms) of metal is produced at the cathode? What is produced at the anode? What is the mass of this product? What is the total number of Faradays of electricity used in the process? (c) One industrial process has an energy consumption of \(18.5 \mathrm{kWh} / \mathrm{kg}\) of \(\mathrm{Mg} .\) How many joules are required per mole ( \(1 \mathrm{kWh}=1\) kilowatt-hour \(=\) \(\left.3.6 \times 10^{6} \mathrm{J}\right) ?\) How does this energy compare with the energy of the following process? $$\mathrm{MgCl}_{2}(\mathrm{s}) \rightarrow \mathrm{Mg}(\mathrm{s})+\mathrm{Cl}_{2}(\mathrm{g})$$

A method recently suggested for the preparation of hydrogen (and oxygen) from water proceeds as follows: (a) Sulfuric acid and hydrogen iodide are formed from sulfur dioxide, water, and iodine. (b) The sulfuric acid from the first step is decomposed by heat to water, sulfur dioxide, and oxygen. (c) The hydrogen iodide from the first step is decomposed with heat to hydrogen and iodine. Write a balanced equation for each of these steps, and show that their sum is the decomposition of water to form hydrogen and oxygen.

The boron atom in boric acid, \(\mathrm{B}(\mathrm{OH})_{3},\) is bonded to three - OH groups. In the solid state, the \(-\mathrm{OH}\) groups are in turn hydrogen-bonded to - OH groups in neighboring molecules. (a) Draw the Lewis structure for boric acid. (b) What is the hybridization of the boron atom in the acid? (c) Sketch a picture showing how hydrogen bonding can occur between neighboring molecules.

Consider the chemistries of the elements potassium, calcium, gallium, germanium, and arsenic. (a) Write a balanced chemical equation depicting the reaction of each element with elemental chlorine. (b) Describe the bonding in each of the products of the reactions with chlorine as ionic or covalent. (c) Draw Lewis electron dot structures for the products of the reactions of gallium and arsenic with chlorine. What are their electron-pair and molecular geometries?

Phosphorus forms an extensive series of oxoanions. (a) Draw a structure, and give the charge for an oxophosphate anion with the formula \(\left[\mathrm{P}_{4} \mathrm{O}_{13}\right]^{\mathrm{n}-} .\) How many ionizable H atoms should the completely protonated acid have? (b) Draw a structure, and give the charge for an oxophosphate anion with the formula \(\left[\mathrm{P}_{4} \mathrm{O}_{12}\right]^{\mathrm{n}-} .\) How many ionizable \(\mathrm{H}\) atoms should the completely protonated acid have?

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