Construct a concept map using the ideas of packing of spheres and the structure of metal and ionic crystals.

Short Answer

Expert verified
A concept map has been constructed, one that identifies the relationships between sphere packing and the crystal structures of metals and ionic compounds, summarizing the principles for three major concepts: packing of spheres, metallic crystals, and ionic crystals. The arrangement of spheres (atoms, ions, molecules) directly influences the structure of crystal formed and each crystal structure has been explained with examples.

Step by step solution

01

Identifying the Concepts

Start by identifying the major concepts: packing of spheres, structure of metal crystals and structure of ionic crystals. These will be the nodes in our concept map.
02

Thinking About Sphere Packing

Next, take the concept of packing of spheres. In a crystal structure, atoms, ions or molecules are often considered as spheres. Their arrangement or packing (close packing or body-centered packing for example) often influences the crystal structure of substances. This is a concept that you should define and provide examples for.
03

Understanding Metal Crystal Structure

Then, for the structure of metal crystals, think about how atoms are arranged in a metal. Metals usually adopt close packing which leads to typical metal crystal structures like face-centered cubic (FCC) or body-centered cubic (BCC). Describe and depict these structures in the concept map.
04

Understanding Ionic Crystal Structure

Finally, when it comes to ionic crystals, the packing and arrangement of ions depends on the relative sizes and charges of the cations and anions. Some common examples of ionic crystal structures include sodium chloride (NaCl) and cesium chloride (CsCl), each of which should be described and shown in the map.
05

Connecting the Concepts

Connection lines or arrows should be drawn between these core concepts showing their interrelationships. On the lines, describe the relationship or connection between the two concepts it connects. For example, connect sphere packing to metal and ionic crystals stating that the mode of sphere packing influences the type of crystal structure.

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Key Concepts

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

Packing of Spheres
Understanding the packing of spheres is fundamental in comprehending various crystal structures.

In its simplest form, 'spheres' in this context refer to the atoms or molecules that make up a given substance. How these spheres are arranged, or 'packed', can greatly influence the properties of the material. There are primarily two types of sphere packing: close packing and body-centered packing. Close packing is where each sphere is in contact with as many neighboring spheres as possible, leading to high-density structures. By contrast, body-centered packing has a central sphere surrounded by others which are not arranged as compactly.

These arrangements are particularly relevant in metal crystals, where close packing leads to densely packed metal atoms in structures like face-centered cubic (FCC) or hexagonal close-packed (HCP) arrangements. In these structures, each metal atom is touched by several neighboring atoms, maximizing spatial efficiency and contributing to the overall strength and stability of the metal.
Metal Crystal Structure
The metal crystal structure is distinctive due to the properties of metals, such as malleability, ductility, and high electrical conductivity.

Metals commonly form two types of crystal lattice structures: face-centered cubic (FCC) and body-centered cubic (BCC). For instance, in FCC, each atom is at the corner of a cube and also at the center of each cube face, resulting in a uniformly dense structure; examples include aluminum and copper. With BCC, there's an atom at each cube corner and one in the center of the cube, but the lattice points do not touch along the face diagonals; examples are iron and chromium.

Knowing the type of lattice structure can help predict various properties of the metal, including how it deforms under stress and its conductivity. Comprehending this specific area of crystallography lays a foundation for further study in material science and engineering.
Ionic Crystal Structure
The ionic crystal structure is characteristic of compounds composed of cations (positively charged ions) and anions (negatively charged ions). Unlike metal crystals, ionic crystals are bound together by the electrostatic attraction between ions of opposite charges.

The arrangement of ions in these crystals depends quite heavily on the size and charge of the ions. For example, in the sodium chloride (NaCl) structure, each sodium ion (Na+) is surrounded by six chloride ions (Cl-) in an octahedral pattern. This is known as a rock-salt structure, a classic example of face-centered cubic packing. In cesium chloride (CsCl), cesium ions (Cs+) and chloride ions (Cl-) form a simple cubic structure, where each ion type forms a separate, interpenetrating cubic lattice.

These structures define not just the physical appearance of the crystal but its melting point, solubility, and hardness. Such knowledge is especially useful in various applications, including the manufacturing of ceramics, batteries, and other electronic components.
Concept Map Creation
The practice of concept map creation is a valuable learning and teaching tool, especially in illustrating connections between complex ideas. A concept map is essentially a visual diagram that depicts the relationships among concepts.

When constructing a concept map for crystal structures, you would begin by drawing nodes for the main concepts: 'packing of spheres', 'metal crystal structure', and 'ionic crystal structure'. These nodes are then connected by lines or arrows to show how these concepts are interrelated. For example, arrows might lead from 'packing of spheres' to both 'metal crystal structure' and 'ionic crystal structure' to signify that the packing heavily influences the properties and types of crystal structures in each material.

On the connecting arrows, brief descriptions will clarify the nature of the relationship. This method not only enhances memory retention by linking ideas visually but also encourages the development of a hierarchical structure in learning, from general to more specific concepts.

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Most popular questions from this chapter

All solids contain defects or imperfections of structure or composition. Defects are important because they influence properties, such as mechanical strength. Two common types of defects are a missing ion in an otherwise perfect lattice, and the slipping of an ion from its normal site to a hole in the lattice. The holes discussed in this chapter are often called interstitial sites, since the holes are in fact interstices in the array of spheres. The two types of defects described here are called point de kcts because they occur within specific sites. In the 1930 s, two solidstate physicists, W. Schottky and J. Fraenkel, studied the two types of point defects: A Schottky defect corresponds to a missing ion in a lattice, while a Fraenkel defect corresponds to an ion that is displaced into an interstitial site. (a) An example of a Schottky defect is the absence of a \(\mathrm{Na}^{+}\) ion in the NaCl structure. The absence of a \(\mathrm{Na}^{+}\) ion means that a \(\mathrm{Cl}^{-}\) ion must also be absent to preserve electrical neutrality. If one NaCl unit is missing per unit cell, does the overall stoichiometry change, and what is the change in density? (b) An example of a Fraenkel defect is the movement of \(a \mathrm{Ag}^{+}\) ion to a tetrahedral interstitial site from its normal octahedral site in \(\mathrm{AgCl}\), which has a structure like \(\mathrm{NaCl}\). Does the overall stoichiometry of the compound change, and do you expect the density to change? (c) Titanium monoxide (TiO) has a sodium chloridelike structure. X-ray diffraction data show that the edge length of the unit cell is \(418 \mathrm{pm}\). The density of the crystal is \(4.92 \mathrm{g} / \mathrm{cm}^{3}\) Do the data indicate the presence of vacancies? If so, what type of vacancies?

Silicone oils, such as $\mathrm{H}_{3} \mathrm{C}\left[\mathrm{SiO}\left(\mathrm{CH}_{3}\right)_{2}\right]_{\mathrm{n}} \mathrm{Si}\left(\mathrm{CH}_{3}\right),$ are used in water repellents for treating tents, hiking boots, and similar items. Explain how silicone oils function.

How many liters of \(\mathrm{CH}_{4}(\mathrm{g}),\) measured at \(23.4^{\circ} \mathrm{C}\) and \(768 \mathrm{mmHg},\) must be burned to provide the heat needed to vaporize 3.78 L of water at \(100^{\circ} \mathrm{C}\) ? \(\Delta \mathrm{H}_{\text {combustion }}=\) \(-8.90 \times 10^{2} \mathrm{kJmol}^{-1} \mathrm{CH}_{4} \quad\) For \(\quad \mathrm{H}_{2} \mathrm{O}(\mathrm{l}) \quad\) at \(\quad 100^{\circ} \mathrm{C}\) \(d=0.958 \mathrm{g} \mathrm{cm}^{-3},\) and \(\Delta H_{\mathrm{vap}}=40.7 \mathrm{kJmol}^{-1}\)

One of the following substances is a liquid at room temperature and the others are gaseous: \(\mathrm{CH}_{3} \mathrm{OH}\) \(\mathrm{C}_{3} \mathrm{H}_{8} ; \mathrm{N}_{2} ; \mathrm{N}_{2} \mathrm{O} .\) Which do you think is the liquid? Explain.

Explain the important distinctions between each pair of terms: (a) adhesive and cohesive forces; (b) vaporization and condensation; (c) triple point and critical point; (d) face-centered and body-centered cubic unit cell; (e) tetrahedral and octahedral hole.

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