Are the following statements true or false? (a) If there is an atom present at the corner of a unit cell, there must be the same type of atom at all the corners of the unit cell. (b) A unit cell must be defined so that there are atoms at the corners. (c) If one face of a unit cell has an atom in its center, then the face opposite that face must also have an atom at its center. (d) If one face of a unit cell has an atom in its center, all the faces of the unit cell must also have atoms at their centers.

Short Answer

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Statement (a) is True. Statement (b) is False. Statement (c) is True. Statement (d) is False.

Step by step solution

01

Evaluating Statement (a)

Assess the claim about atom consistency at the corners of a unit cell. In a crystal lattice, the unit cell corners are shared with adjacent unit cells. Therefore, if a particular atom is at one corner, the same type of atom must be at all the corners due to the repeating pattern throughout the crystal.
02

Evaluating Statement (b)

Determine if a unit cell necessarily contains atoms at its corners. A unit cell is the smallest repeating unit that completely describes the lattice structure. While it is common for atoms to be at the corners of unit cells, it is not a requirement for defining a unit cell. Thus, a unit cell can be defined without having atoms at the corners.
03

Evaluating Statement (c)

Verify if an atom at the center of one face necessitates an atom at the center of the opposite face. When atoms are positioned at face centers in a unit cell, each of these atoms is shared with the neighboring unit cell. It follows that if an atom exists at the center of one face of the unit cell, the face opposite must also have an atom at its center for the structure to be consistent.
04

Evaluating Statement (d)

Investigate the claim about atom placement on all faces when one face has an atom in its center. The presence of an atom at the center of one face does not imply that all the other faces of a unit cell will also have atoms at their centers. The structure depends on the type of unit cell and is not universally applicable.

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Key Concepts

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

Crystal Lattice
The concept of a crystal lattice is fundamental in understanding the solid-state structure of materials. A crystal lattice can be envisioned as an orderly three-dimensional arrangement of points that extends infinitely in all directions. Each point, referred to as a lattice point, represents the position of an atom, ion, or molecule within that crystal structure. Think of it like a 3D grid where each intersection point is where you would find the constituent particles of the crystal.

These lattice points are not random; they follow a specific pattern that repeats throughout the entirety of the crystal. This pattern defines the internal structure of the material and its symmetry. Imagine a wall built from perfectly identical bricks where each brick's position is predictable and consistent throughout. The precise and repetitive nature of a crystal lattice is what gives crystals their unique and often visually stunning properties, such as facets and symmetry.
Atom Placement
The arrangement of atoms within a crystal lattice is the subject of atom placement. Atoms can be situated in several locations within a unit cell: at the corners, on the edges, at the face centers, or within the body of the unit cell. The rules governing this placement are critical for defining the physical and chemical properties of the material.

For example, when an atom is placed at a corner of a unit cell, it is actually shared among eight adjacent unit cells in a three-dimensional lattice. This means that although you might place one atom at a corner, in calculation, each unit cell only 'owns' one eighth of that atom. Similarly, an atom placed at the center of a face is shared with just the neighboring unit cell, hence, each 'owns' half of that atom. These placements and their resultant shared ownership result in precise formulas for determining the number of atoms within a single unit cell and ultimately contribute to the stoichiometry of the material.
Lattice Structure
A lattice structure is the geometric arrangement of the points of a crystal lattice and how these points are occupied by atoms. The symmetry and spacing of these lattice points are described by the unit cell, which can vary in shape and size depending on the intrinsic nature of the material.

There are seven main types of unit cell geometries, or crystal systems: cubic, tetragonal, orthorhombic, hexagonal, trigonal, monoclinic, and triclinic. Each of these systems exhibits different symmetries and lattice parameters. For instance, in a cubic structure, the length of the unit cell edges are all equal and the angles are all right angles. In contrast, a triclinic structure has no sides of equal length and no angles that are the same. The variations between lattice structures help in classifying materials and understanding their macroscopic properties, such as cleavage patterns, optical properties, and mechanical strength.
Repeating Unit in Crystals
The concept of the repeating unit in crystals is epitomized by the term 'unit cell'. A unit cell is the smallest portion of the crystal lattice that retains the full symmetry and properties of the entire crystal. This means that by stacking the unit cells together in all three dimensions, you can build the macroscopic crystal. It's like having a single blueprint that, when repeated, constructs the entire edifice of a structure.

In practice, identifying the repeating unit is fundamental when analyzing the crystal structure. It simplifies calculations, such as determining the density of a crystal, predicting its thermal expansion, or assessing its potential behaviors under external forces. Each unit cell is like a 3D puzzle piece, fitting snugly with others of its kind to create the uniform and continuous entity we recognize as a crystal.

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Most popular questions from this chapter

Tetrahedral and octahedral interstitial holes are formed by the vacancies left when anions pack in a ccp array. (a) Which hole can accommodate the larger ions? (b) What is the size ratio of the largest metal cation that can occupy an octahedral hole to the largest that can occupy a tetrahedral hole while maintaining the close-packed nature of the anion lattice? (c) If half the tetrahedral holes are occupied, what will be the empirical formula of the compound \(\mathrm{M}_{x} \mathrm{~A}_{y}\), where \(\mathrm{M}\) represents the cations and \(\mathrm{A}\) the anions?

Draw the Lewis structure of (a) \(\mathrm{NI}_{3}\) and (b) \(\mathrm{BI}_{3}\), name the molecular shape, and indicate whether each can participate in dipole- dipole interactions.

Suggest, giving reasons, which substance in each of the following pairs is likely to have the higher normal melting point (Lewis structures may help your arguments): (a) \(\mathrm{HCl}\) or \(\mathrm{NaCl}\); (b) \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OC}_{2} \mathrm{H}_{5}\) (diethyl ether) or \(\mathrm{C}_{4} \mathrm{H}_{9} \mathrm{OH}\) (butanol); (c) \(\mathrm{CH}_{3}\) or \(\mathrm{CHF}_{3} ;\) (d) \(\mathrm{C}_{2} \mathrm{H}_{4}\) or \(\mathrm{CH}_{3} \mathrm{OH}\).

Suggest, giving reasons, which substance in each of the following pairs is likely to have the higher normal boiling point: (a) \(\mathrm{H}_{2} \mathrm{~S}\) or \(\mathrm{H}_{2} \mathrm{O}\); (b) \(\mathrm{NH}_{3}\) or \(\mathrm{PH}_{3}\); (c) \(\mathrm{KBr}\) or \(\mathrm{CH}_{3} \mathrm{Br}\); (d) \(\mathrm{CH}_{4}\) or \(\mathrm{SiH}_{4}\).

One form of silicon has density of \(2.33 \mathrm{~g} \cdot \mathrm{cm}^{-3}\) and crystallizes in a cubic lattice with a unit cell edge of \(543 \mathrm{pm}\). (a) What is the mass of each unit cell? (b) How many silicon atoms does one unit cell contain?

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