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In your own words, define the following terms: (a) dimer; (b) adduct; (c) calcination; (d) amphoteric oxide; (e) three-center two-electron bond.

Short Answer

Expert verified
A dimer is a complex formed from two identical, simpler molecules. An adduct is a product of a direct addition of two or more distinct molecules. Calcination is the process of heating a substance to cause thermal decomposition, or the removal of a volatile substance. An amphoteric oxide can act as either an acid or a base in a reaction. A three-center two-electron bond is a kind of covalent bond where three atoms are involved, and two electrons are shared among them.

Step by step solution

01

Defining Dimer

A dimer refers to a complex that is formed from two identical, simpler molecules. These two molecules connect, usually through a process known as dimerization.
02

Defining Adduct

An adduct is a product of a direct addition of two or more distinct molecules, resulting in a single reaction product. The resulting entity contains all the atoms of all the original molecules.
03

Defining Calcination

Calcination refers to the process of heating a substance in order to cause thermal decomposition, a phase transition, or the removal of a volatile substance. It is often used in the removal of carbonate to produce lime from limestone.
04

Defining Amphoteric Oxide

An amphoteric oxide is an oxide that can act as either an acid or a base in a reaction. That is, it can either donate protons (acting as an acid) or accept protons (acting as a base). Metallic oxides are usually basic, and non-metallic oxides are usually acidic, but a few, like aluminum oxide (Al2O3), are amphoteric.
05

Defining Three-center Two-electron Bond

Three-center two-electron bond is a kind of covalent bond where three atoms are involved, and two electrons are shared among them. The best-known examples of compounds that contain three-center two-electron bonds are boron hydride clusters, such as diborane(6) [B2H6].

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Key Concepts

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

Understanding Dimers
Dimers are fascinating chemical structures found throughout chemistry, especially pertinent in biomolecules where they can affect the biological activity. A dimer, simply put, is a molecule consisting of two similar or identical molecules linked together. These tandems are not random; they occur through a process known as dimerization, often involving a bond between atoms or a non-covalent interaction like hydrogen bonding, which is particularly common in biological systems.

One classic example of a dimer is the way two nucleic acid bases bond in the structure of DNA, vital for genetic inheritance. In industry, dimers play a role in polymer sciences, where the initiation step often involves dimerization. Understanding this concept helps grasp foundational chemistry involved in complex synthesis and structural formation.
Adducts and their Role
In chemistry, an adduct is akin to a guest mingling with the host at a molecular soiree. Formed from the union of two or more different molecules, an adduct is a single reaction product that retains all the atoms from the combining entities.

The bonds in adducts are typically covalent, and their formation marks the conclusion of reactions such as coordination and catalysis. For example, in coordination complexes, a central metal atom joined by several ligands is essentially forming an adduct. This detail aids in predicting and understanding reactivity, stability, and properties of complexes in inorganic chemistry and beyond.
Calcination in Material Processing
Calcination is not merely heating; it is a deliberate thermal process used in materials science to induce change. Often part of metallurgical and ceramic processes, calcination involves heating materials to a high temperature in the absence or limited supply of air or oxygen.

This technique can remove volatile fractions from materials, enact thermal decomposition or facilitate a phase transition. An everyday example is the conversion of limestone, composed mainly of calcium carbonate (CaCO3), into lime (CaO) while releasing carbon dioxide (CO2). Solutions to problems involving calcination can elucidate the thermal behavior of materials, crucial for fields such as materials engineering and geochemistry.
Amphoteric Oxides and Their Dual Nature
Chemistry often presents materials with dual characteristics, and amphoteric oxides are perfect examples. These oxides have the unique ability to behave as both acids and bases, meaning they can either donate or accept protons based on the reaction conditions.

The concept of amphoteric behavior is essential in understanding the reactivity and applications of certain metal oxides, such as aluminum oxide (Al2O3) or zinc oxide (ZnO), which can interact with both acids and bases. This characteristic is also relevant in environmental chemistry and technology, where amphoteric oxides play roles in neutralizing acidic or basic pollutants.
Three-center Two-electron Bond: A Unique Connection
A leap from standard bonds, the three-center two-electron (3c-2e) bond represents an extraordinary type of bonding where three atoms share two electrons in a bonding arrangement. This bond is an aspect of many electron-deficient compounds and a frequent feature in boron clusters like in diborane (B2H6).

In this molecular relationship, the electrons are delocalized over the three centers, creating a bond that is less typical than the conventional two-center two-electron (2c-2e) bonds found in most organic compounds. Understanding these bonds provides insights into the stability and structure of electron-deficient compounds. Knowledge of 3c-2e bonds is essential in fields involving the study of boranes, carboranes, and similar substances, which have distinctive properties and applications not seen in more conventional molecules.

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Most popular questions from this chapter

The Gibbs energies of formation, \(\Delta G_{\mathrm{f}}^{\circ},\) for \(\mathrm{Na}_{2} \mathrm{O}(\mathrm{s})\) and \(\mathrm{Na}_{2} \mathrm{O}_{2}(\mathrm{s})\) are \(-379.09 \mathrm{kJ} \mathrm{mol}^{-1}\) and \(-449.63 \mathrm{kJ} \mathrm{mol}^{-1}\) respectively, at 298 K. Calculate the equilibrium constant for the reaction below at \(298 \mathrm{K} .\) Is \(\mathrm{Na}_{2} \mathrm{O}_{2}(\mathrm{s})\) thermodynamically stable with respect to \(\mathrm{Na}_{2} \mathrm{O}(\mathrm{s})\) and \(\mathrm{O}_{2}(\mathrm{g})\) at \(298 \mathrm{K} ?\) $$ \mathrm{Na}_{2} \mathrm{O}_{2}(\mathrm{s}) \longrightarrow \mathrm{Na}_{2} \mathrm{O}(\mathrm{s})+\frac{1}{2} \mathrm{O}_{2}(\mathrm{g}) $$

Which has the (a) higher melting point, MgO or BaO; (b) greater solubility in water, \(\mathrm{MgF}_{2}\) or \(\mathrm{MgCl}_{2}\) ? Explain.

Lithium superoxide, \(\mathrm{LiO}_{2}(\mathrm{s}),\) has never been isolated. Use ideas from Chapter \(12,\) together with data from this chapter and Appendix \(D\), to estimate \(\Delta H_{f}\) for \(\mathrm{LiO}_{2}(\mathrm{s})\) and assess whether \(\mathrm{LiO}_{2}(\mathrm{s})\) is thermodynamically stable with respect to \(\mathrm{Li}_{2} \mathrm{O}(\mathrm{s})\) and \(\mathrm{O}_{2}(\mathrm{g}).\) (a) Use the Kapustinskii equation, along with appropriate data below, to estimate the lattice energy, \(U,\) for \(\left.\mathrm{LiO}_{2}(\mathrm{s}) . \text { (See exercise } 126 \text { in Chapter } 12 .\right)\) The ionic radii for \(L\) i \(^{+}\) and \(O_{2}^{-}\) are \(73 \mathrm{pm}\) and \(144 \mathrm{pm},\) respectively. (b) Use your result from part (a) in the BornFajans-Haber cycle to estimate \(\Delta H_{\mathrm{f}}^{2}\) for \(\mathrm{LiO}_{2}(\mathrm{s})\) [Hint: For the process \(\mathrm{O}_{2}(\mathrm{g})+\mathrm{e}^{-} \rightarrow \mathrm{O}_{2}^{-}(\mathrm{g}), \Delta H^{\circ}=.\) \(-43 \mathrm{kJ} \mathrm{mol}^{-1} .\) See Table 21.2 and Appendix \(\mathrm{D}\) for the other data that are required.] (c) Use your result from part (b) to calculate the enthalpy change for the decomposition of \(\mathrm{LiO}_{2}(\mathrm{s})\) to \(\mathrm{Li}_{2} \mathrm{O}(\mathrm{s})\) and \(\mathrm{O}_{2}(\mathrm{g}) .\) For \(\mathrm{Li}_{2} \mathrm{O}(\mathrm{s}), \Delta H_{\mathrm{f}}^{\circ}=-598.73\) \(\mathrm{kJmol}^{-1}.\) (d) Use your result from part (c) to decide whether \(\mathrm{LiO}_{2}(\mathrm{s})\) is thermodynamically stable with respect to \(\mathrm{Li}_{2} \mathrm{O}(\mathrm{s})\) and \(\mathrm{O}_{2}(\mathrm{g}) .\) Assume that entropy effects can be neglected.

The best oxidizing agent of the following oxides is (a) \(\mathrm{Li}_{2} \mathrm{O} ;(\mathrm{b}) \mathrm{MgO} ;(\mathrm{c}) \mathrm{Al}_{2} \mathrm{O}_{3} ;(\mathrm{d}) \mathrm{CO}_{2} ;(\mathrm{e}) \mathrm{SnO}_{2} ;(\mathrm{f}) \mathrm{PbO}_{2}.\)

In the purification of bauxite ore, a preliminary step in the production of aluminum, \(\left[\mathrm{Al}(\mathrm{OH})_{4}\right]^{-}(\mathrm{aq})\) can be converted to \(\mathrm{Al}(\mathrm{OH})_{3}(\mathrm{s})\) by passing \(\mathrm{CO}_{2}(\mathrm{g})\) through the solution. Write an equation for the reaction that occurs. Could HCl(aq) be used instead of \(\mathrm{CO}_{2}(\mathrm{g}) ?\) Explain.

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