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Molecular solids: water, argon.
Ionic solids: potassium sulphate, zinc sulphate.
Metallic solids: tin, rubidium.
Covalent or network: benzene, urea, ammonia, graphite, silicon carbide.
Ionic solids do not conduct electric current in solid state because in the solid ionic compound, the ions are held together in fixed positons by strong electrostatic forces and cannot move freely.
Ionic solids conduct electricity in liquid state because the crystal structure is broken down and ions become free to move and conduct electricity.
(i) Each point in a lattice is called lattice point or lattice side.
(ii) Each point in a crystal lattice represents one constituent particle which may be an atom, a molecule or an ion.
(iii) Every lattice point has identical surroundings except those which are on the surface or corner of a crystal.
(iv) If a line is drawn by joining two lattice points, it would pass through a series of similar points at regular intervals.
(v) Lattice points are joined by straight lines to bring out the geometry of the lattice. These lines do not represent chemical bond.
Unit cell is the smallest portion of a crystal lattice.
A unit cell is characterized by:
(i) its dimensions along the three edges a, b and c. These edges may or may not be mutually perpendicular.
(ii) angles between the edges, α (between b and c), β (between a and c),γ (between a, and b). Thus, a unit cell is characterised by six parameters, a, b, c, α, β and γ.
Ans. (i) Hexagonal Unit cell Monoclinic unit cell
(1) Axial distances or edge
lengths a = b ≠ c a ≠ b ≠ c
(2) Axial angles α = β = 90° α = γ=90° β ≠ 90°
(3) Examples: Graphite, ZnO, CdS Monoclinic Sulphur, PbCrO2,
Na2SO4.10H2O
2 4 2
(ii) Face centered unit cell |
End-centered unit cell |
It contains one particle present at the centre of its each face, besides the ones that are at its corners. |
In this unit cell, one constituent particle is present at the centre of any two opposite faces besides the ones present at its corners. |
(i) Primitive cubic unit cell has atoms only at its corner. Each atom at a corner is shared between eight adjacent unit cells . four unit cells in the same layer and four unit cells of the upper (or lower) layer Therefore only 1/8th of an atom (molecule or ion) actually belongs to a particular unit cell.
since each cubic unit cell has 8 atoms on its corners, the total number of atoms in one unit cell is atom.
(ii) The atom at the body centre wholly belongs to the unit cell in which it is present. Thus in a body-centered cubic (bcc) unit cell:
(i) 8 corners per corner atom =
(ii) 1 body centre atom =
therefore total number of atom per unit cell =2 atom.
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body-centred cubic
C.
hexagonal close packed latticeHexagonal close packed lattice has the highest packing efficiency (74%).
Non-stoichiometric defects can arise when a solid is heated.
The crystals with this defect becomes coloured. Alkali halides like NaCl and KCl show this type of defect. When crystals of NaCl are heated in an atmosphere of sodium vapour, the sodium atoms are deposited on the surface of the crystal. The CI– ions diffuse to the surface of the crystal and combine with Na atoms to give NaCl. This happens by loss of electron by sodium atoms to form Na+ ions. The released electrons diffuse into the crystal and occupy an ionic sites. As a result the crystal now has an excess of sodium. They impart yellow colour to the crystals of NaCl.
(i) Frenkel defect.
(ii) Schottky defect and Frenkel defect.
(iii) Schottky defect.
Number of Z per unit cell = 1/8 x 8Z = 1 Z.
Number of X per unit cell = 1 Y.
Formula of the compound = ZY.
The maximum coordination number is 12 in hcp crystal .
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In a body centred unit cell diagonal contain two extra atom .so in per unit cell =
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How many lattice points are there in one unit cell of each of the following lattice?
(a) face centred cubic
(b) face centred tetragonal
(c) body centred cubic
A face-centred cubic (fcc) unit cell contains atoms at all the corners and at the centre of all the faces of the cube.each atom located at the face-centre is shared between two adjacent unit cells and only 1/2 of each atom belongs to a unit cell
Thus, in a face-centred cubic
(fcc) unit cell:
(i) 8 corners atoms × 1/8 atom per unit cell = 8×1/8 = 1 atom
(ii) 6 face-centred atoms ×1/2 atom per unit cell = 6 ×1/2 = 3 atoms
∴ Total number of atoms per unit cell = 4 atoms
body centre wholly belongs to the unit cell in which it is present. Thus
in a body-centered cubic (bcc) unit cell:
(i) 8 corners × 1/8 per corner atom= 8×1/8 = 1 atom
(ii) 1 body centre atom = 1 × 1 = 1 atom
∴ Total number of atoms per unit cell =1+1 = 2
(c) z = 2.
A face-centred cubic (fcc) unit cell contains atoms at all the corners and at the centre of all the faces of the cube.
It can be seen that each atom located at the face-centre is shared between two adjacent
unit cells and only1/2 of each atom belongs to a unit cell.
The number of atoms present at corners per unit cell= 8 corner atoms x 1/8 atoms per unit cell = 1
The number of atoms present at faces per unit cell
= 6 atoms at the faces x 1/2 atoms per unit cell
= 6 x 1/2 = 3 atoms
Therefore, total number of atoms per unit cell = 4 atoms.
When crystals of NaCl are heated in an atmosphere of sodium vapour, the sodium atoms are deposited on the surface of the crystal.
The Cl– ions diffuse to the surface of the crystal and combine with Na atoms to give NaCl. This happens by loss of electron by sodium atoms to form Na+ ions. The released electrons diffuse into the crystal and occupy anionic sites and impart colour.
Let the number of close packed spheres be N, then:
The number of octahedral voids generated = N
The number of tetrahedral voids generated = 2N
What is the two-dimentional coordination number of a molecule in square closed packed layer ?
A face-centred cubic (fcc) unit cell contains atoms at all the corners and at the centre of all the faces of the cube. It can be seen that each atom located at the face-centre is shared between two adjacent
unit cells and only 1/2 of each atom belongs to a unit cell.
Thus, in a face-centred cubic
(fcc) unit cell:
(i) 8 corners atoms × 1/8 atom per unit cell=8×1/8
= 1 atom
(ii) 6 face-centred atoms ×
1/2 atom per unit cell = 6 ×1/2 = 3 atoms
∴ Total number of atoms per unit cell = 4 atoms
Solids having constituent particles with irregular shapes and short range order are called amorphous solids. Amorphous solids are isotropic in nature and melt over a range of temperature. Thus, amorphous solids are also referred as pseudo solids or super cooled liquids.
Amorphous solids do not have definite heat of fusion.
Amorphous solids give irregular surfaces, when cut with sharp tool.
Glass, rubber, plastic, etc. are some examples of amorphous solid.
It is the arrangement of constituent particles of glass which makes it different from quartz. The constituent particles of glass have short range order while quartz has constituent particles in long range order and short range order both.
By heating and cooling rapidly quartz can be converted into glass.
Property |
Quartz |
Glass |
1. Structure 2. Melting point |
Quartz is crystalline and it has long range order. Quartz has a sharp melting point. It changes into viscous liquid at 1983 K. |
Amorphous silica does not have a regular structure of long range order. Glass does not have a sharp melting point. On heating it softens and melts over a wide range of temperature. |
(i) Tetra phosphorous decoxide (P4O10)
(ii) Ammonium phosphate (NH4)3PO4
(iii) SiC
(iv) I2
(v) P4
(vi) Plastic
(vii) Graphite
(viii) Brass
(ix) Rb
(x) LiBr
(xi) Si
Solution:
(i) Tetra phosphorous decoxide (P4O10) - Molecular
(ii) Ammonium phosphate (NH4)3PO4 – Ionic
(iii) SiC - Covalent (network)
(iv) I2 - Molecular
(v) P4 - Molecular
(vi) Plastic - Amorphous
(vii) Graphite – Covalent (network)
(viii) Brass - Metallic
(ix) Rb - Metallic
(x) LiBr - Ionic
(xi) Si – Covalent (network)
(ii) What is the coordination number of atoms:
(a) in a cubic close-packed structure?
(b) in a body-centred cubic structure?
(ii) The coordination number of atoms
(a) In a cubic close-packed structure is 12
(b) In a body-centered cubic structure is 8
Solution:
The atomic mass of an unknown metal can be determined by knowing its density and the dimension of unit cell.
'Stability of a crystal is reflected in the magnitude of its melting points. Comment. Collect melting points of solid water, ethyl alcohol, diethyl ether and methane from a data book. What can you say about the inter molecular forces between these molecules?
Solution:
Stability of a crystal is reflected in the magnitude of its melting points because higher the melting point, greater is the intermolecular force and greater the intermolecular force greater is the stability. And hence, a substance with higher melting point would be more stable.
The melting points of the given substances are as follows:
Solid water - 273 K
Ethyl alcohol – 158.8 K
Diethyl ether – 156.85 K
Methane – 89.34 K
As we can see the melting point of solid water is highest and melting point of methane is lowest among the given substance. This says that intermolecular force in solid water is strongest and the intermolecular force in methane is weakest.
Solution:
(i) One unit cell of a face-centered cubic has 8 lattice points are corners and 6 lattice points at faces, total 14 lattice points.
(ii) One unit cell of face-centered tetragonal has 8 lattice points are corners and 6 lattice points at faces, total 14 lattice points.
(iii) One unit cell of body centered has 8 lattice points are corners and 1 lattice points at faces, total 9 lattice points.
Explain the basis of similarities and differences between metallic and ionic crystals.
Characteristics |
Ionic crystals |
Metallic crystals |
|
1. |
Constituent particles |
cations (positive ions) and anions (negative ions) |
Positive ions and mobile electrons. |
2. |
Binding forces |
Strong electrostatic forces (electro valent bonding) |
Electrical attraction between positive ions and mobile electrons (metallic bonding) |
3. |
Physical properties |
Hard and brittle; high m.p. and b.p. good conductors of heat and electricity in molten state and aqueous solution, high heat of fusion. |
Hard but malleable, high m.p., very good conductors of heat and electricity in solid and molten state, moderate heats of fusion. |
Explain Ionic solids are hard and brittle.
Metal excess defect due to the presence of extra cations at interstitial sites: Zinc oxide is white in colour at room temperature. On heating it loses oxygen and turns yellow
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When crystals of NaCl are heated in an atmosphere of sodium vapour, the sodium atoms are deposited on the surface of the crystal.
The Cl– ions diffuse to the surface of the crystal and
combine with Na atoms to give NaCl. This happens by loss of electron by sodium atoms to form Na+ ions. The released electrons diffuse into the crystal and occupy anionic sites. As a result the crystal now has an excess of sodium. The anionic sites occupied byunpaired electrons are called F-centre. They impart yellow colour to the crystals of NaCl.
The colour results by excitation of these electrons when they absorb energy from the visible light falling on the crystals.
Solution:
Semiconductor: - Solids having intermediate range of conductivity, i.e. from 10–6 to 104 ohm–1 m–1 are called semiconductors. Semiconductors are of following two types:
(i) n – type of semiconductors
(ii) p – type of semiconductors
(i) n – type semiconductors – Semiconductors formed after doping with electron rich impurities to increase their conductivity are called n-type of semiconductors.
Example –
Silicon and germanium, each has four valence electrons as they belong to 14th group of periodic table. Arsenic and phosphorous belong to 15th group of periodic table and they have valence electrons equal to 5. When silicon or germanium is doped with phosphorous or arsenic, four electrons of phosphorous or arsenic out of five; make covalent bonds with four electrons of silicon or germanium leaving one electron free; which increases the electrical conductivity of silicon or germanium.
n-type semi-conductor.
Since the electrical conductivity of silicon or phosphorous is increased because of negatively charged particle (electron), thus this is known as n-type of semiconductor.
(ii) p – type of semiconductor - Semiconductors formed by the doping with electron deficient impurities; to increase their conductivity; are called p-type semiconductors. In p - type of semiconductors, conductivity increase because of formation of electron holes.
Example - Electrical conductivity of silicon or germanium is doped with elements, such as Boron, Aluminium or Gallium having valence electrons equal to 3. Three valence electrons present in these elements make covalent bonds with three electrons present in valence shell out of four of silicon or germanium leaving one electron delocalized. The place from where one electron is missing is called electron hole or electron vacancy.
When the silicon or germanium is placed under electrical field, electron from neighbouring atom fill the electron hole, but in doing so another electron hole is created at the place of movement of electron. In the influence of electrical filed electron moves toward positively charge plate through electron hole as appearing the electron hole as positively charged and are moving towards negatively charged plate.
p-type semi-conductor.
Schottky defects |
Frenkel defects |
1. It arises due to vacancy at a cation site and at a nearby anion site in an ionic solid. 2. Overall density of the crystal decreases. 3. It arises in ionic solids having high co-ordination number. |
1. It arises when a cation leaves its lattice site and enters in an interstitial site in an ionic solid. 2. There is no change in the overall density. 3. It arieses in ionic solids having large anions and small cations. Example: ZnS, AgCl, AgI etc |
In the given figure, let an sphere having centre ‘O’ is fitted in the octahedral void.
As given, radius of the sphere fitted in the octahedral void = r
And radius of the atoms in close packing = R
Phosphorus has one excess valence electron (compared with Si) after forming the four covalent bonds normally with silicon. This excess electron gives rise to electronic conduction. That is why silicon becomes semi-conductor on doping with phosphorus. It is called n-type semi-conductor.
Gallium has only three valence electrons. It creates an electron deficient bond or a hole when it is doped with silicon. Such holes can move in the crystal giving rise to electrical conductivity. Thus silicon doped with gallium is also semi-conductor due to movement of holes. It is called-p-type semiconductor.
Paramagnetic substances are attracted by the magnetic field. This is due to the presence of unpaired electrons in the atoms/ions/molecules of the paramagnetic substance. Paramagnetism is a temporary effect.
Ferromagnetic substances are strongly attracted by the magnetic field. They show magnetism even when the magnetic field is removed. This is due to a spontaneous alignment of the magnetic dipole in the same direction.
Transition metal compounds contains one or more unpaired electrons. So, these compounds show para magnetism. The paramagnetism of the bivalent ions of the first transition metal series first increases in going from Ti2+ to Mn2+ (number of unpaired electrons increases) and then decreases upto Cu2+ (because the number of unpaired electrons decreases).
Transition metal compounds contains one or more unpaired electrons. So, these compounds show para magnetism. The paramagnetism of the bivalent ions of the first transition metal series first increases in going from Ti2+ to Mn2+ (number of unpaired electrons increases) and then decreases upto Cu2+ (because the number of unpaired electrons decreases).
In the sample of cuprous oxide, Cu2O prepared in laboratory, copper to oxygen ratio is less than 2 : 1 and this deficiency of copper causes the metal deficiency defects.
In these defects the positive ions are less in number as compared to anions. These defects are caused in two ways:
(i) By Cation Vacancies : Some Cu+ may be missing from lattice sites and their positive charges are balanced by presence of extra charge on adjacent cations i.e., some Cu2+ are present and some cation vacancies are present.
(ii) By presence of extra anions at interstitial sites: The type of defect can arise where some oxide ion, O2– are present at lattice sites and their charge is balanced by neighbouring cations in higher oxidation states i.e., some Cu2+ ions are present instead of Cu2+ ions.
Metal deficiency defect due cation vacancy.
Metal deficiency defect due to presence of extra anions.
Let us Suppose the number of oxide (O2–) ions = N.
Number of octahedral void = number of anions
So that the number of octahedral voids = N
We have Given that
Two out of every three octahedral holes are occupied by ferric ions.
So that the number of ferric (Fe3+) ions = 2N/3
The ratio of the number of Fe3+ ions to the number of O2− ions,
Fe3+ : O2− = 2N/3 : N
Multiply 3 and divide by N we get
Fe3+ : O2− = 2 : 3
Hence, the formula of the ferric oxide is Fe2O3.
(i) Ge is an element of 14th group (like Si) and has configuration 4s24p2. It has been doped with In, a 13th group element having 5s25p1 configuration i.e., element of 14th group has been doped with 13th group element. All three valence electrons of impurity atom (In) gets bonded with three out of four eectrons of Ge and one electron of Ge remains unbonded. Conductivity is due to unbonded electron of insulator, Ge. Therefore, it is a p-type semi-conductor.
(ii) Boron, B is an element of 13th group and has 2s22p1 configuration. It is doped with Si, an element of 14th group having 3s23p2 configuration. All three electrons of boron gets bonded with 3 out of 4 electrons of Si and 4th electron of impurity atom (i.e., Si) is responsible for conductivity. Thus it is a n-type semiconductor.
In terms of band theory, what is the difference between a conductor and an insulator?
Solution:
Molecular orbirals of metals are formed by atomic orbitals. These orbitals are so close to each other as they form band or valence band.
(i) Difference between conductor and insulator - In conductors there is no energy gap between the valence band, which facilitates the flow of electrons easily under an applied electric field and metals show conductivity.
While in insulators there is large energy gap between the valence band and electrons cannot jump to it i.e. large energy gap prevents the flow of electricity.
(ii)Difference between conductors and semiconductor - In conductors there is no energy gap between the valence band and conduction band, which facilitates the flow of electrons easily under an applied electric field and metals show conductivity.
While in semi conductors, there is small energy gap between valence bond and conduction band. The small gap between band facilitates some electrons to jump to the conduction band by acquiring extra energy.
In terms of band theory, what is the difference between a conductor and a semi-conductor?
Semiconductor: In instrinsic semiconductors, the energy gap, Eg, is relatively small (≈ = 1 eV). At absolute zero, conduction band is empty and valence band is full. Therefore, the solid behaves as an insulator at very low temperatures. However, at room temperature, some electrons from the top of valence band acquires enough thermal energy to jump into the conduction band. They leave behind a number of holes. Both electrons and holes movement contribute to conduction.
In extrinsic semi-conductor of n-type, the donor energy level is close to the bottom of conduction band.
In p-type the acceptor energy level is close to the top of valence band.
Schottky defects : When cations and anions both are missing from regular sites, the defect is called Schottky Defect. In Schottky Defects, the number of missing cations is equal to the number of missing anions in order to maintain the electrical neutrality of the ionic compound.
Schottky Defect is type of simple vacancy defect and shown by ionic solids having cations and anions; almost similar in size, such as NaCl, KCl, CsCl, etc. AgBr shows both types of defects, i.e. Schottky and Frenkel Defects.
Since, Schottky Defects arises because of mission of constituent particles, thus it decreases the density of ionic compound.
.It is a type of vacancy defect. In ionic compounds, some of the ions (usually smaller in size) get dislocated from their original site and create defect. This defect is known as Frenkel Defects. Since this defect arises because of dislocation of ions, thus it is also known as Dislocation Defects. As there are a number of cations and anions (which remain equal even because of defect); the density of the substance does not increase or decrease.
Ionic compounds; having large difference in the size between their cations and anions; show Frenkel Defects, such as ZnS, AgCl, AgBr, AgI, etc. These compounds have smaller size of cations compared to anions.
(i) These type of vacancy defects are called Schottky defects.
(ii) This defect decreases the density of the crystal.
(iii) NaCl shows this type of defect in the crystalline state.
(iv) This is the point defect which does not disturb stoichiometry of the solid.
It changes into paramagnetic at hight temperature due to randomization of spins.
(b) The ions in MgO carry two unit charges. In NaCl only one unit charge. Hence electrostatic forces of attraction in MgO are stronger.
We have,
Edge of length of cell a = 4.07x10–8cm
Density p = 10.5 g /cm3
Number of atoms in unit cell of fcc lattice = 4
Avogadro number NA = 6.022x1023
By using formula,
We have give that,
Density (d)=8.55 g Cm-3
Atomic mass (M) =93u =93 gMol-1
Atomic radius (r) = ?
We know that, Avogadro number Na =6.022 x 10 23 mol-1
since given lattice is bcc
therefore
Number of atoms per unit cell (z) =2
we know that
We have given that
Length of edge, a = 3.61x10–8 cm
Atomic mass of cupper, M = 63.55 g/mol
Avogadro constant, NA = 6.022x1023 per mol
Number of atoms in unit cell of FCC, Z= 4
Use formula of density,
Formula is Ni0.98O1.00
So the ration of Ni : O = 98:100
So if there are 100 atoms of oxygen then 98 atoms of Ni,
Let number of atoms of Ni+2 = x
Then number of atoms of Ni+3 = 98–x
Charge on Ni = charge on O
So that oxygen has charge –2
3(98–x) + 2x = 2 (100)
294 –3x +2x = 200
–x = – 94
x = 94
Percentage of Ni+2 = (atom of Ni+2/total number of atoms of Ni)100
=100(94/98)x100
= 96%
Percentage of Ni+3
=100 – Ni+2
=100 – 96
= 4 %
Gold (atomic radius = 0.144 nm) crystallises in a face-centred unit cell. What is the length of a side of the cell?
Given, radius of atom (r) = 125 pm
(a) For ccp structure, we know that,
We know that two Na+ ions are replaced by each of the Sr2+ ions while SrCl2 is doped with NaCl. But in this case, only one lattice point is occupied by each of the Sr2+ ions and produce one cation vacancy.
Here 10 – 3 mole of SrCl2 is doped with 100 moles of NaCl Thus, cation vacancies produced by NaCl = 10 – 3 mol Since, 100 moles of NaCl produces cation vacancies after doping = 10 –3 mol
Therefore, 1 mole of NaCl will produce cation vacancies after doping
=
therefore, total cationic vacancies
=10-5 x Avogadro's number
=10-5 x 6.023 x 1023
=6.023 x 10-18 vacancies
Solution:
We have given
volume of the unit cell = (5 x 10-8cm)3 = 1.25 x 10-22cm3
Density of FeO = 4g cm-3
Density,
Each unit cell has four units of FeO. So it has four Fe2+ and four O2– ions.
solution:
we have given a= 2.88A0
Density = 7.20g cm-3
mass = 100g
Volume of the unit cell =
Volume of 100g of the metal
No. of unit cell in
solution:
we have given
Density of element,
Cell edge a= 314pm or 3.14 x 10-10 cm
Atomic mass
The structure of the crystal lattice is B.C.C.
Solution:
we have given that
density, d= 7.2g cm-3
edge = 288 x 10-10 cm
NA = 6.02 x 1023
for Bcc structure Z= 2
Atomic mass = ?
Thus, atomic mass of element is =51.77 g/mol
Solution:
We have given that
Gram atomic mass of Cr(M) = 52.0 g mol-1
Edge length of unit cell (a) = 289 pm
Density of unit cell = 7.2 g cm-3
Avogadro's Number
or
Since the unit cell has 2 atoms, it is body centre in nature.
Volume of the unit cell = (5 A°)
= (5 x 10–8 cm)3
= 125 x 10–24 cm3
= 1.25 x 10–22 cm3
Density of FeO = 4.0 g cm–3
Therefore, mass of the unit cell
= 1.25 x 10–22 cm3 x 4 g cm–3
= 5 x 10–22g
Mass of all molecules of FeO
Number of FeO molecules/unit cell
Thus, there are 4 Fe2+ ions and 4O2– ions in each unit cell.
Solution:
We have given that
Unit cell length,
a = 0.40806 nm = 4.086 x 10-10 m
If fcc lattice the number of atoms per unit cell,
i.e. Z = 4
M for Ag = 107.88 g mol-1
Solution:
We have given that
Edge length of the unit cell
= 200 pm = 200 x 10–10 cm
Vol. of the unit cell
= (200 x 10–10 cm)3 = 8 x 10–24 cm3
Therefore, volume of the substance
= Vol. of unit cell x Vol. of 1 unit cell.
Since the element has a fcc unit cell, number of atoms per unit cell = 4.
Total number of atoms = Atoms/unit cell x number of unit cells.
= 24 x 1023atoms = 4
atoms/unit cell x No. of unit cells.
∴ No. of unit cells =
∴ Volume of the substance
Now,
Solution:
We have given that
Density = 10 gm-3
Mass = 100g
edge of unit cell ,a= 4 since it is a Fcc crystal
we have to find total number of atom, So by following relation we can get the result,
Total No. of atoms =
Therefore, number of atoms
thus the number of atoms is 4 x 1031
Solution:
M0.98 O1.00 is non-stoichiometric compound and is a mixture of M2+ and M3+ ions.
Let x atoms of M3+ are present in the compound. This means that x M2+ have been replaced by M3+ ions.
∴ Number of M2+ ions = 0.96 – x.
For electrical neutrality, positive charge on compound
= negative charge on compound.
∴ 2(0.96 – x) + 3x = 2
1.92 – 2x + 3x = 2
or x = 2 – 1.92 = 0.08
∴
Thus, M2+ is 92% and M3+ is 8% in given sample having formula, M0.96 O1.00.
Or
The number of tetrahedral voids formed is equal
to twice the number of atoms of element N and only of these are occupied by the element M. Hence the ratio of number of atoms of M and is So, the formula of the compound is M2N3.
Solution:
(i) Simple Cubic: A simple cubic unit cell has one sphere (or atom) per unit cell. If r is the radius of the sphere, then volume occupied by one sphere present in unit cell =
Edge length of unit cell (a) = r + r = 2r
Volume of cubic
Volume of occupied by sphere =
Percentage volume occupied = percentage of efficiency of packing
For simple cubic metal crystal the efficiency of packing = 52.4%.
(b) Body centred cubic: From the figure it is clear that the atom at the centre will be in touch with other two atoms diagonally arranged and shown with solid boundaries.
The length of the body diagonal c is equal to 4r where r is the radius of the sphere (atom). But c = 4r, as all the three spheres along the diagonal touch each other
∴
or
or
Fig. BCC unit cell. In this sort of structure total number of atoms is two and their volume is
Volume of the cube, a3 will be equal to
Therefore, Percentage of efficiency Volume occupied by four - spheres
(c) Face centred cubic: A face centred cubic cell (fcc) contains four spheres (or atoms) per unit volume occupied by one sphere of radius
r = 4/3 r3
Volume occupied by four spheres present in the unit cell
r = 4/3 r3 x 4 = 16/3 r3
Fig. Face centred cubic unit cell. Figure indicates that spheres placed at the corners touches a face centred sphere. Length of the face diagonal
= r + 2r + r = 4r
Hence, for face centred cubic, efficiency of packing = 74%.
Piezoelectric effect (or pressure electricity):
The word piezoelectricitymeans electricity resulting from pressure.
Insulators do not conduct electricity be the electrons present in them are held tightly to the individual atoms or ions and do not move. However, when an electric field is applied polarisation takes place and newly formed dipoles may align themselves in an ordered manner so that such crystals have a net moment.
When mechanical stress is applied on a polar crystals so as to deform them, electricity produced due to displacement of ions. This is known as piezoelectric effect and electric so this produced is known as Piezo electricity or pressure electricity. Example are : titanium, barium and lead, lead zirconate (PbZrO3), ammonium dihydrogen phosphate and quartz.
Solid ionic compounds do not conduct electricity because the ions (charged particles) are locked into a rigid lattice or array. The ions cannot move out of the lattice, so the solid cannot conduct electricity.
When molten, the ions are free to move out of the lattice structure.
When an ionic solid is dissolved in water to form an aqueous solution, the ions are released from the lattice structure and are free to move so the solution conducts electricity just like the molten (liquid) ionic compound.
coordination number
Density of crystal is lowered by shottky defect.
Schottky defect decrease the density solid where as no such defect arise due to frenkel defect.
The maximum possible coordination number of an atom in hcp structure of an element is 12.
Body centre wholly belongs to the unit cell in which it is present. Thus
in a body-centered cubic (bcc) unit cell:
(i) 8 corners × 1/8per corner atom= 8 x 1/8 = 1 atom
(ii) 1 body centre atom = 1 × 1 = 1 atom
∴ Total number of atoms per unit cell = 2 atoms
For face centred
(i) 8 corners atoms × 1/8 atom per unit cell
= 8 x1/8 = 1 atom
(ii) 6 face-centred atoms ×1/2 atom per unit cell = 6 ×1/2 = 3 atoms
∴ Total number of atoms per unit cell = 4 atoms
arsenic (As) or phosphorus (P).
2Na+ will replaced by Mg2+ ion to maintain electrical neutrality thus ahole created for lattice site for every Mg2+ ion introduce thus the defect produced will schottky defect
When ferromagnetic substance is subjected to high temperature it loses its magnetic property and become paramagnetic in nature this happen due to disorder ness in electronic arrangment.
Cadium chloride is substance which on addition to AgCl cause cation vacancy in it.
Alkali metal halides have anionic sites occupied by unpaired electrons. These are called F-centres, and impart colour to the crystals of alkali metal halides. For example, the excess of lithium in LiCl makes it pink.
Shottkey defect can lower the density of a crystal.
Coordination number of CCP is 12.
Potassium, rubidium.
In an alloy of gold and cadmium, gold crystallizes in cubic structure occupying the corners only and cadmium fits into the face centre voids.
Number of gold atoms =1/8 x 8 =1Au
Number of candium atoms =1/2 x 6 =3Cd
Hence, quantitative composition on = AuCd3
Both naturally-occurring and artificial quartz crystal contains at least ninety-nine percent silicone dioxide, while cut glass crystal only possesses at most eighty percent silicone dioxide.
Compounds having frenkel defect conduct electricity to a small extent. When electric field is applied, an ion moves from its lattice site to occupy a hole, it creates a new hole. In this way, a hole moves from one end to the other. Thus, it conducts electricity across the crystal. Due to the presence of holes, stability (or the lattice energy) of the crystal decreases.
When doping a semiconductor, such as the group IV element silicon (Si), with arsenic (As), a pentavalent n-type dopant from group V in the periodic table the dopant behaves as an electron donor.
In ferromagnetic materials, neighboring dipoles tend to line up in the same direction, whereas in ferrimagnetic materials, neighboring dipoles tend to line up in opposing directions.
Schottky Defect lowers the density of ionic crystal.
(i) When silicon is doped with phosphorus four valence electrons of phosphorus are involved in bond formation with the neighbouring silicon atoms, while the fifth valence electron is left free to conduct electricity. This type of conduction which arises due to the availability of excess electrons is called n-type conduction.
(ii) Schottky defect arises when equal number of cations and anions are missing from their lattice sites. As the number of ions decreases due to this defect In order to maintain electrical neutrality, the number of missing cations and anions are equal, the mass decreases, but the volume remains the same. As a result, the density of the solid decreases.
(iii) Some of the very old glass objects appear slightly milky instead of being transparentbecause of some crystallisation at that point.
Semiconductors : These are the solids with conductivities in the intermediate range from 10–6 to 104 ohm–1m–1.
In case of semiconductors, the gap between the valence band and conduction band is small Therefore, some electrons may jump to conduction band and show some conductivity. Electrical conductivity of semiconductors increases with rise in temperature, since
more electrons can jump to the conduction band. Substances like silicon and germanium show this type of behaviour and are called intrinsic semiconductors.
The conductivity of these intrinsic semiconductors is too low to be of practical use. Their conductivity is increased by adding an appropriate amount of suitable impurity. This process is called doping.
There are two types of semiconductor
i) n- type semiconductor
ii) p- type semiconductor
Element of group14 of the periodic table, when doped with a group 15 element like P or As, Four out of five electrons are used in the formation of four covalent bonds with the four neighbouring silicon atoms. The fifth electron is extra and becomes delocalised.
These delocalised electrons increase the conductivity of doped silicon (or germanium). Here the increase in conductivity is due to the negatively charged electron, hence silicon doped with electron-rich impurity is called n-type semiconductor.
p-type :
Silicon or germanium can also be doped with a group 13 element like B, Al or Ga which contains only three valence electrons. The place where the fourth valence electron is missing is called electron hole or electron vacancy. This hole can be act as charge carrier in the lattice. This known as p - type semiconductor.
The coordination number of an atom, ion or molecule is the number of constituent particles which touch that particular atom, atom or molecule.
i) The coordination number of cubic close packed structure is 12.
ii) The coordination number of body-centred cubic structure is 8.
Let ‘a’ be the edge length of the unit cell and r be the radius of sphere.
As sphere are touching each other
Therefore a = 2r
No. of spheres per unit cell = 1/8 × 8 = 1
Volume of the sphere = 4/3 πr3
Volume of the cube = a3= (2r)3 = 8r3
∴ Fraction of the space occupied = 1/3πr3 / 8r3 = 0.524
∴ % occupied = 52.4 %
(a) Determine the type of cubic lattice to which a given crystal belongs if it has edge length of 290 pm and density is 7.80 g cm–3. (Molecular mass.= 56 g mol–1)
(b) Why does zinc oxide exhibit enhanced electrical conductivity on heating?
we know that
as we have given
d= 7.80 g cm–3.
M=56 g mol–1
a= 290 pm or a3 =2.43 x10-23
putting all value in above equation we get,
hence it belong to bcc crystal lattice.
b) Zinc oxide is white in colour at room temperature. On heating it loses electron and turns yellow in colour.
The electron liberate after heating, can act as charge carrier and thus on heating zinc oxide it exhibit electrical conductivity.
Formula mass of CuCl =63.5 +35.5
= 99.0
The number of formula units per cell of ZnS is 4. It has face centred cubic structure.
we have given,
Mass= 209 g
Number of atom per unit cell =1 (Simple cubic)
density =91.5 g m-3
NA =6.023 x1023
edge length of unit cell =?
By applying formula
a= 15.59 x10-8 cm
we have
edge length =200Pm
volume of the unit = ( 200 x10-10 cm)3
= 8 x10-24 cm-3
density = 41.6 g cm-3.
we have given :
mass of silver = 107.87 g
Z(FCC) = 4
distance between nearest neighbour Ag atoms = 2.87 x10-10
we have given,.
mass =108 g
edge (a) = 409pm
a3 = 6.84 x1023 cm3
Na =6.023 x10-233
Z =4
Apply formula
density = 10.98 g cm–3
length of the unit cell edge = 400Pm =400x10-10 cm
volume of the unit cell = ( 400 x10-10cm)3
= 6.4 x 10-23 cm-3
as the element A forms a body centred cubic lattice so no of atom per units cell is 2
z= 2 atoms unit cell
atomic mass of the element =100 g/mol
density of element is given by
we have give that aluminium forms Fcc cubic crystal.
density = 2.7g cm-3
Mass of aluminium = 27g
number of unit cell =4 (FCC)
we have find edge length
Thus using formula
we know that
as given that,
density= 2.75 g cm–3
a = 654 pm or a3 = 2.79 x 10-23
mass of KBr is 119 gram
we have given,
density =19.35 g cm-3
edge length =316 pm
Number of unit cell =2 (BCC)
Mass =?
Thus,
In a unit cell there are one Cs and 1 x 8/8 =1 chlorine (Cl-) such that one CsCl molecule
therefore
As we have given
density = 3.97 g cm-3
Mass of CsCl = 168.36g
Number of unit cell(Z) = 1
for a cube of side length 4.13A0 diagonal
=
as it is a BCC with Cs+ at centre radius r+ and Cl- at corner radius r- so,
2r+ +2r- =7.15 or r+ +r- =3.57A0
such that distance between neighbouring Cs+ and Cl- =3.57A0
now assume two Cl- ion touch with each other so length of unit cell = 2r- =4.13
r- =2.06A0
r+ =3.57 -2.06 =1.51
r+/r-=1.51/2.06 =0.73
i) A crystalline solid usually consists of a large number of small crystals, each of them having a definite Characteristic geometrical shape. In a crystal, the arrangement of constituent particles (atoms, molecules or ions) is ordered. It has long range order which means that there is a regular pattern of arrangement of particles which repeats itself periodically over the entire crystal. Sodium chloride and quartz are typical examples of crystalline solids.
ii) Crystalline solid have a sharp melting point.
Crystalline solids can be classified on the basis of nature of intermolecular forces operating in them into four categories.
i) molecular
ii)ionic
iii)metallic
iv)covalent solids.
i) molecular: Molecules are the constituent particles of molecular solids. These are further sub divided into the following categories:
a) Non polar Molecular Solids: They comprise of either atoms, for example, argon and helium or the molecules formed by non polar covalent bonds for example H2, Cl2.
b) Polar Molecular Solids: The molecules in which solids are held together by relatively stronger dipole-dipole interactions.for example HCl, SO2, etc.
c) Hydrogen Bonded Molecular Solids: The molecules of such solids contain polar covalent bonds between H and F, O or N atoms. Strong hydrogen bonding binds molecules of such solids like H2O (ice).
ii) Ionic solid : Ions are the constituent particles of ionic solids. In ionic solid cations and anions bound by strong coulombic (electrostatic) forces. for example NaCl, KCl etc.
iii) metallic solid: These solids contain metal atoms as constituent particles. As metals have a good tendency to lose their valence electron and change in to positively charged metal ions (kernel). These electrons can easily move throughout the whole crystal and form the sea of free electrons. for example iron, calcium etc.
iv) covalent solids: A wide variety of crystalline solids of non-metals result from the formation of covalent bonds between adjacent atoms throughout the crystal. They are also called giant molecules. for example diamond, silicon carbide, etc.
i) CsCl is simple cubic cell. Cesium ion is surrounded by eight chloride ion which are also disposed towards the corner of a cube therefore both type ions are in equivalent positions and the stoichiometry is 1:1 . the coordination of CsCl is 8:8.
ii) Zinc sulfide is a FCC unit cell. The net number of zinc cation per unit cell is four, and the net number of sulfide anions per unit cell is four therefore, the ratio of ZnS ion in the cell is 1:1.
iii)Calcium fluoride is a FCC unit cell. The net number of Calcium cation per unit cell is four and the net number of fluoride anion is eight. Therefore the ratio of CaF2 ion in cell is 1:2
iv) Na2O has the structure opposite to CaF2. In
this case coordination number of Na+ ions is 4 and that of O2- ion is 8. Thus Na2O has 4:8 coordination.
a) Frenkel defect is not found in the pure alkali metal halides because this defect is due to vacancy of ion ,which is shifted in interstitial spaces and because the ions are too large and cannot get into interstitial sites.
b) ZnO becomes yellow on heating due to frankel defect, when ZnO is heated, it loses oxygen reversibly and turns yellow in colour.
Zno + heat -->Zn2+ +1/O2 +2e-
The Zn2+ ions formed the vacant voids in the crystal to form non- stoichiometric solid. The released electrons are trapped in its neighborhood. It is therefore non-stoichiometric ZnO is yellow and shows increased conductivity.
c) The free electrons trapped in the anion vacancies are called as F-centers. Solids containing F-centres are paramagnetic because the electrons occupying the vacant sites are unpaired.
d) Uncharged molecules and atoms are packed more efficiently in closed-packet structures. Hence theses uncharged molecules and atoms do not crystallize in simple cubic structures.
e) In both the structure, the fraction of the total volume occupied is 0.74. The two structure have the same coordination number of 12.
What is the formula of a compound in which the element Y forms ccp lattice and atoms of X occupy 1/3rd of tetrahedral voids?
Number of tetrahedral voids formed = 2 x Number of atoms of element Y
Number of atoms of element Y in the ccp unit cell = 4
Number of tetrahedral voids formed = 2 x 4 = 8
Number of tetrahedral voids occupied by atoms of X = 1/3x8
Ratio of the numbers of atoms of X and Y = 8/3: 4 =2: 3
Hence, the formula of the compound is X2Y3.
An element with molar mass 27 g mol-1 forms a cubic unit cell with edge length 4.05 x 10-8 cm . If its density is 2.7 g cm-3 , what is the nature of the cubic unit cell?
Molar mass of the given element, M = 27 g mol-1 = 0.027 kg mol-1
Edge length, a = 4.05 x 10-8 cm = 4.05 x 10-10 m
Density, d = 2.7 g cm-3 = 2.7 x 103 kg m-3
Applying the relation,
Where, Z is the number of atoms in the unit cell and NA is the Avogadro number. Thus,
Since the number of atoms in the unit cell is four, the given cubic unit cell has a face-centred cubic (fcc) or cubic-closed packed (ccp) structure.
An element with density 11.2 g cm-3 forms a f.c.c. lattice with edge length of 4 x10-8
Calculate the atomic mass of the element. (Given: NA = 6.022x 10-23 (mol-1)
Density, d = 11.2 g cm-3
Edge length, a = 4x10-8 cm
Avogadro number, NA = 6.022x1023 mol-1
Number of atoms present per unit cell, Z (fcc) = 4
We know for a crystal system,
Thus, the atomic mass of the element is 107.91 g.
Examine the given defective crystal:
Answer the following questions:
(i) What type of stoichiometric defect is shown by the crystal?
(ii) How is the density of the crystal affected by this defect?
(iii) What type of ionic substances shows such defect?
(i) Schottky defect is shown by the mentioned crystal, as an equal number of cations and anions are missing in the crystal lattice.
(ii) This defect leads to decrease in density, as an equal number of the cations and anions are missing from the crystal lattice. A number of such defects in ionic solids are quite significant. For example, in NaCl, there are approximately 106 Schottky pairs per cm3 at room temperature.
(iii) This kind of defect is shown by that ionic substance in which the cations and anions are of almost similar sizes.
Examples: NaCl, KCl and CsCl.
How many atoms constitute one unit cell of a face-centered cubic crystal?
Number of atoms in one face centred cubic unit cell can be determined:-
(i) 8 corners atoms × 1/8 per corner atom = = 1 atom
(ii) 6 face-centered atoms × 1/ 2 atom per unit cell = = 3 atoms
∴ Total number of atoms per unit cell = 4 atoms
(a) What type of semiconductor is obtained when silicon is doped with boron?
(b) What type of magnetism is shown in the following alignment of magnetic moments?
(c) What type of point defect is produced when AgCl is doped with CdCl2?
(a) When silicon is doped with boron, a p-type semiconductor is obtained.
(b) The magnetism shown in the alignment of magnetic moments is ferromagnetism.
Ferromagnetism is the basic mechanism by which certain materials (such as iron) form permanent magnets, or are attracted to magnets.
(c) Impurity defect is produced when AgCl is doped with CdCl2.
What is meant by ‘doping’ in a semiconductor?
Doping is the process of increasing the conductivities of the intrinsic semiconductors by adding suitable impurity.
Iron has a body centred cubic unit cell with a cell dimension of 286.65 pm. The density of iron is 7.874 g cm-3. Use this information to calculate Avogadro's number (At. Mass of Fe = 55.845 u)
a = 286.65 pm
a= 286.65 x 10-10cm
Density ( ) = 7.874 g cm-3
At mass of Fe = 55.845 u
Z = 2 (For body centred cubic unit cell)
Avogadro number (N0) =?
‘Crystalline solids are anisotropic in nature’. What does this statement mean?
All crystalline solids are not anisotropic. Those crystalline solids which are anisotropic have their atoms arranged and spaced in a different manner in three different planes (X, Y and Z). Therefore, the physical properties of crystalline solids such as electrical resistance or refractive index show different values when measured along different directions in the same crystals.
Example NaCl, Quartz, Ice, HCl, Iron, etc.
Silver crystallizes in face-center cubic unit cell. Each side of this unit cell has a length of 400 pm. Calculate the radius of the silver atom. (Assume the atoms just touch each other on the diagonal across the face of the unit cell. That is each face atom is touching the four corner atoms.)
Given, silver crystallizes in fcc unit cell
So,
Define the following terms:
(i) Primitive unit cells
(ii) Schottky defect
(iii) Ferromagnetism
(i) Primitive unit cells are defined as the unit cells in which the constituent particles are present only at the corner positions.
(ii) Schottky defect: Schottky defect is basically a vacancy defect shown ionic solids. In this defect, an equal no cation and anion are missing to maintain electrical neutrality. It decreases the density of a substance. An Ionic substance containing the similar size of cations and anion show this type of defect. For example: NaCl, KCl, CsCl, AgBr, etc.
(iii) Ferromagnetism is defined as the phenomenon in which substances, such as iron, cobalt and nickel, are strongly attracted by a magnetic field. Such substances are called ferromagnetic substances.
(a) Why does the presence of an excess of lithium make LiCl crystals pink?
(b) A solid with cubic crystal is made of two elements P and Q. Atoms of Q are at the corners of the cube and P at the body-center. What is the formula of the compound?
(a) When crystals of LiCl is heated in presence of excess of lithium, Cl- ions from crystal diffuse on the surface and combine with ionized Li to form LiCl. The released unpaired electrons occupy the anionic sites known as F-centers. The pink colour results by excitation of these electrons when they absorb energy from visible light falling on them.
(b) It is given that the atoms of Q are present at the corners of the cube. Therefore, number of atoms of Q in one unit cell =
Also, it is also given that the atoms of P are present at the body-center.
Therefore, number of atoms of P in one unit cell = 1
This means that the ratio of the number of P atoms to the number of Q atoms, P: Q = 1:1
Hence, the formula of the compound is PQ.
Aluminum crystallizes in an fcc structure. Atomic radius of the metal is 125 pm. What is the length of the side of the unit cell of the metal?
Aluminum crystallizes in FCC structure atomic radius (r) = 125 pm
Length of the side of the unit cell in FCC structure,
Therefore a= 2 x 1.414 x 125
a = 353.5 pm
What are n-types semiconductors?
The semiconductor whose increased conductivity is a result of negatively-charged electrons is called an n-type semiconductor. These are generated when the crystal of a group 14 element such as Si or Ge is doped with a group 15 element such as P or As.
Copper crystallises with face centred cubic unit cell. If the radius of a copper atom is 127.8 pm, calculate the density of the copper metal.
(Atomic mass of Cu = 63.55 u and Avogadro’s number NA = 6.02 x 1023 mol-1)
No. of atoms in unit cell, Z = 4
Radius = 127.8 pm
Iron has a body centred cubic unit cell with the cell dimension of 286.65 pm. The density of iron is 7.87 g cm-3. Use this information to calculate Avogadro’s number. (Atomic mass of Fe = 56.0 u)
a = 286.65 pm
= 286.65 x 10-10 cm
Density (Ï) = 7.874 g cm-3
At mass of Fe = 56.0 u
Z = 2 (For body centered cubic unit cell)
Avogadro number (N0) =?
What type of magnetism is shown by a substance if magnetic moments of domains are arranged in same direction?
When the magnetic moments of domains are arranged in the same direction then, the substance shows ferromagnetism.
Given an example each of molecular solid and an ionic solid.
(i) Molecular Solid - I2
(ii) Ionic Solid - NaCl
An element crystallizes in b.c.c lattice with cell edge of 500 pm. The density of the element is 7.5g cm-3. How many atoms are present in 300 g of the element ?
We have given,
a= 500pm
d=7.5 g cm-3
mass = 300g
Calculate the packing efficiency of a metal crystal for a simple cubic lattice.
In a simple cubic lattice, the particles are located only at the corners of the cube and touch each other along the edge.
In a simple cubic lattice, the particles are located only at the corners of the cube and touch each other along the edge.
Let the edge length of the cube be ‘a’ and the radius of each particle be r.
So, we can write:
a = 2r
Now, volume of the cubic unit cell = a3 = (2r)3 = 8r3
We know that the number of particles per unit cell is 1.
Therefore, volume of the occupied unit cell =
Explain how you can determine the atomic mass of an unknown metal if you know its mass density and the dimensions of a unit cell of its crystal.
By knowing the density of an unknown metal and the dimension of its unit cell, the atomic mass of the metal can be determined.
Let ‘a’ be the edge length of a unit cell of a crystal, ‘d’’ be the density of the metal, ‘m’ be the atomic mass of the metal and ‘z ’ be the number of atoms in the unit cell.
An element with density 2.8 g cm−3 forms of the f.c.c. unit cell with edge length 4 X10−8 cm. Calculate the molar mass of the element.
(Given: NA = 6.022 X 1023 mol −1)
Edge length, a = 4 x 10-8 cm
Density, d = 2.8 g cm-3
As the lattice is fcc type, the number of atoms per unit cell, z is 4.
Avogadro's number, NA = 6.022 x 1023 mol-1
Molar mass can be calculated with the help of given relation:
(i) What type of non-stoichiometric point defect is responsible for the pink colour of LiCl?
(ii) What type of stoichiometric defect is shown by NaCl?
OR
How will you distinguish between the following pairs of terms:
(i) Tetrahedral and octahedral voids
(ii) Crystal lattice and unit cell.
i) The pink colour of LiCl is because of the metal excess defect caused by the anionic vacancies.
ii) NaCl shows Schottky defect. In the Schottky defect, an equal number of cations and anion are missing from their regular sites.
Or
(i) Tetrahedral void surrounded by four spheres is called a tetrahedral void.
Octahedral void surrounded by six spheres is called an octahedral void.
(ii) Crystal lattice: A crystal lattice is a diagrammatic representation of the constituent particles such as atoms, ions and molecules of a crystal in a regular three-dimensional arrangement.
Unit cell: A unit cell is the smallest three-dimensional portion of a crystal lattice. When it is repeated in different directions, it generates the entire crystal lattice.
An element has atomic mass 93 g mol–1 and density 11.5 g cm–3. If the edge
the length of its unit cell is 300 pm, identify the type of unit cell.
Given,
M= 93 g mol-1
d= 11.5 g cm-3
a = 300 pm = 300 x 10-10 cm = 3 x 10-8
We know that,
The number of atoms present in given unit cells is coming nearly equal to 2. Hence, the given unit cell is body centred cubic unit cell (BCC).
Write any two differences between amorphous solids and crystalline solids.
Property | Crystalline Solids | Amorphous solids |
Arrangement of Constituent particles | Regular | Irregular |
Isotropy | Regular Cleavage | Irregular Cleavage |
Examples | Diamond, Quartz, Copper Sulphate, Sodium Chloride etc | Glass, Rubber, Wood, Amorphous Silica |
Calculate the number of unit cells in 8.1 g of aluminium if it crystallizes in a
f.c.c. structure. (Atomic mass of Al = 27 g mol–1)
Given
Mass of Al =8.1
Atomic mass of Al = 27 g mol-1
Number of atoms = Number of moles x 6.022 x1023
As one fcc unit has 4 atoms
Hence number of unit cells having 1.8066 x1023 atoms
Give reasons :
In stoichiometric defects, NaCl exhibits Schottky defect and not Frenkel
defect.
NaCl, cation has large size thus it can not fit into voids so thus not show Frankel defect.
Give reasons :
Silicon on doping with Phosphorus forms the n-type semiconductor.
Give reason:
Ferrimagnetic substances show better magnetism than antiferromagnetic
substances.
In the presence of magnetic field, the magnetic moments of domains of an antiferromagnetic substances are ordered in such a way half of the magnetic moments are aligned in one direction while the remaining half is in opposite direction. As a result of it, a net magnetic moment will be zero whereas in case of ferrimagnetic substances the magnetic moments of the domains of ferrimagnetic substances are aligned in parallel and antiparallel directions in unequal numbers. As a result, there will be the small value of magnetic moment for ferrimagnetic substances.
Analysis shows that FeO has a non-stoichiometric composition with formula Fe0.95O. Give reason.
The non-stoichiometry reflect the ease of oxidation of Fe2+ to Fe3+ effectively replacing a small portion of Fe2+ with two thirds their number of Fe3+. Thus for every three 'missing' Fe2+ ions, the crystal contains two Fe3+ ions to balance the charge. i.e. 3Fe2+ = 2Fe3+ to maintain electrical neutrality.
Which of the following compounds is metallic and ferromagnetic?
VO2
MnO2
TiO2
CrO2
D.
CrO2
Only three elements iron (Fe) cobalt (Co) and Nickel (Ni) show ferromagnetism at room temperature. CrO2 is also a metallic and ferromagnetic compound which is used to make magnetic tapes for cassette recorders
Sodium metal crystallises in a body centred cubic lattice with a unit cell edge of 4.29 Å The radius of sodium atom is approximate:
1.86 Å
3.22Å
5.72 Å
0.93 Å
A.
1.86 Å
According to the figure
(AC)2 = (AB)2 + (BC)2
(AC)2 = a2 + a2 = 2a2
(AD)2 = (AC)2+ (DC)2
(4r)2 = 2a2 + a2
CsCl crystallises in body centred cubic lattice. If 'a' its edge length, then which of the following expression is correct?
C.
In CsCl, Cl- lie at corners of simple cube and Cs+ at the body centre, Hence, along the body diagonal, Cs+ and Cl- touch each other so
Lithium forms body centred cubic structure. The length of the side of its unit cell is 351 pm. Atomic radius of the lithium will be
75 pm
300 pm
240 pm
152 pm
D.
152 pm
In body centred cubic structure,
Edge length = a = 351 pm, radius= r=?
The edge length of a face centred cubic cell of an ionic substance is 508 pm. If the radius of the cation is 110 pm, the radius of the anion is
144 pm
288 pm
398 pm
618 pm
A.
144 pm
For FCC lattice (assuming cation in octahedral void and anion in FCC)
a = 508 pm
(r+ + r-) = a/2 = 508/2 = 254 pm
(r+ + r-) = 254 pm
r- = 254-110 = 144 pm
Percentages of free space in cubic close packed structure and in body centred packed structure are respectively
48% and 26%
30% and 26%
26% and 32%
32% and 48%
C.
26% and 32%
Packing fraction of ccp is 74%
% free space in ccp = 26%
Packing fraction of bcc is 68%
%free space in bcc = 32%
A metal crystallises in a face centred cubic structure. If the edge length of its unit cell is'a', the closest approach between two atoms in metallic crystal will be
2a
D.
In FCC unit cell atoms are in constant along face diagonal
So, √2a = 4R
therefore, the closest distance
In a compound atoms of element Y from ccp lattice and those of element X occupy 2/3rd of tetrahedral voids. The formula of the compound will be
X4Y3
X2Y3
X2Y
A.
X4Y3
No. of atoms of Y = 4
No. of atoms of X = 2 x (8/3)
Formula of compound will be X4Y3
Lattice energy of an ionic compounds depends upon
Charge on the ion only
Size of the ion only
Packing of ions only
Charge on the ion and size of the ion
D.
Charge on the ion and size of the ion
Based on lattice energy and other considerations which one of the following alkali metal chlorides is expected to have the highest melting point.
LiCl
NaCl
KCl
RbCl
B.
NaCl
Although lattice energy of LiCl higher than NaCl but LiCl is covalent in nature and NaCl ionic thereafter, the melting point decreases as we move NaCl because the lattice energy decreases as a size of alkali metal atom increases (lattice energy ∝ to melting point of alkali metal halide)
What type of crystal defect is indicated in the diagram below?
Frenkel defect
Frenkel and Schottky defects
Interstitial defect
Schottky defect
D.
Schottky defect
When the equal number of cations and anions are missing. Then it is the case of Schottky defect.
Which type of ‘defect’ has the presence of cations in the interstitial sites?
Metal deficiency defect
Schottky defect
Vacancy defect
Frenkel defect
D.
Frenkel defect
In Frenkel defect, smaller ion displaces from its actual lattice site into the interstitial sites.
Lithium has a bcc structure. Its density is 530 kg m-3 and its atomic mass is 6.94 g mol-1. Calculate the edge length of a unit cell of lithium metal. (NA = 6.02 x 1023 mol-1).
352pm
527pm
264pm
154pm
A.
352pm
Given, Li has a bcc structure
Density (ρ) =530 kg-m-3
atomic mass (M) = 6.94 g mol-1
Avogadro's number of atoms per unit cell in bcc (Z) = 2.
∴ we have the formula for density.
A given metal crystallises out with a cubic structure having edge length of 361 pm. If there are four metal atoms in one unit cell, what is the radius of one atom.
40 pm
127 pm
80 pm
108 pm
B.
127 pm
Given, edge length = 361 pm
Four metal atoms in one unit cell
i.e effective number in unit cell (z) = 4 (given)
therefore,
It is a FCC structure
Face diagonal = 4r
If a is the length of the side of a cube, the distance between the body centred atom and one corner atom in the cube will be
D.
In bcc, 2 atoms are present. One atom lies the centre of the cube while other lies at the corner of the cube. Hence, the distance between the body centred and one corner atom is half of the body diagonal, i.e.,
The number of carbon atoms per unit cell of diamond unit cell is
4
8
6
1
B.
8
The diamond lattice contains an fcc Bravias point lattice which has two identical atoms per lattice point.
The diamond lattice contains 4 lattice points per unit cell but contains 8 atoms per unit cell.
A metal has a fcc lattice. The edge length of the unit cell is 404 pm. The density of the metal is 2.72 g cm-3. The molar mass of the metal is (NA Avogadro's constant= 6.02 x 1023 mol-1)
40 g mol-1
30 g mol-1
27 g mol-1
20 g mol-1
C.
27 g mol-1
Given, cell is fcc, So Z =4
Edge length, a = 404 pm = 4.04 x 10-8 cm
Density of metal, d = 2.72 g cm-3
NA = 6.02 x 1023 mol-1
Molar mass ofg the metal, M =?
We know that
Which of the following statements about the interstitial compounds is incorrect?
They retain metallic conductivity
They are chemically reactive
They are much harder than the pure metal
They have higher melting points than the pure metal
B.
They are chemically reactive
Interstitial compounds are obtained when small atoms like H, B, C, resemebleN etc.fit into the lattice etc. fit into the lattice of other elements. These retain metallic conductivity resemble their parent metal in chemical properties (reactivity)but differ in physical properties like hardness, melting point etc.
The number of octahedral voids (s) per atom present in a cubic close-packed structure is
1
3
2
4
A.
1
A number of octahedral voids = a number of atoms in the close-packed structure. Since number of atoms= 1
So, number of octahedral voids = 1
A structure of a mixed oxide is cubic close packed (ccp). The cubic unit cell of mixed oxide is composed of oxide ions. One fourth of the tetrahedral voids are occupied by divalent metal A and the octahedral voids are occupied by a monovalent metal B. The formula of the oxide is
ABO2
A2BO2
A2B3O4
AB2O2
D.
AB2O2
According to ccp,
Number of O2- ions = 4
So, tetrahedral void = 8
and octahedral void = 4
Since A ions occupied 1/4th of the tetrahedral void.
Therefore,
Number of A ions = 1/4 x 8 = 2
Again, B ions occupied all octahedral void.
Therefore, Number of B ions = 4
A: B:O = 2:4:4
= 1:2:2
Structure of oxide= AB2O2
The correct statement regarding defects in the crystalline solid is
Schottky defects have no effect on the density of crystalline solid
Frenkel defect decreases the density of crystalline solids
Frenkel defect is a dislocation defect
Frenkel defect is found in halides of alkaline metals
C.
Frenkel defect is a dislocation defect
In Frenkel defect, ions in solid dislocate from their position. Hence, Frenkel defect is a dislocation defect.
The vacant space in bcc lattice cell is
26%
48%
23%
32%
D.
32%
Packing efficiency in bcc lattice = 68%
Vacant space in bcc lattice = 100-68 = 32%
AB crystallises in a body centred cubic lattice with edge length 'a' equal to 387 pm. The distance between two oppositely charged ion in the lattice is
335 pm
250 pm
200 pm
300 pm
A.
335 pm
For body centred cubic (bcc) lattice, distance between two oppositely charged ions,
Copper crystallises in a face-centered cubic lattice with a unit cell length of 361 pm. What is the radius of copper atom in pm?
128
157
181
108
A.
128
In case of the face-centred cubic lattice,
radius =
therefore, Radius of the copper atom (fcc lattice)
=
Lithium metal crystallises in a body centred cubic crystal. If the length of the side of the unit cell lithium is 351 pm, the atomic radius of the lithium will be
240.8 pm
151.8 pm
75.5
300.5 pm
B.
151.8 pm
In case of body centred cubic (bcc) crystal,
Hence, atomic radius of lithium,
Volume occipied by one molecule of water (density = 1 g cm-3) is
9.0 x 10-23
6.023 x 10-23 cm3
3.0 x 10-23 cm3
5.5 x 10-23 cm3
C.
3.0 x 10-23 cm3
6.02 x 1023 molecules of water = 1 mol
= 18 g
Therefore, Mass of one molecule of water
Which of the following statements is not correct?
The fraction of the total volume occupied by the atoms in a primitive cell is 0.48
molecules solids are generally volatile
the number of carbon atoms in a unit cell
The number of Bravais latices in which a crystal can be categorised is 14
A.
The fraction of the total volume occupied by the atoms in a primitive cell is 0.48
D.
The number of Bravais latices in which a crystal can be categorised is 14
Packing fraction of lattice structure or fraction of total volume occupied
If 'a' stands for the edge length of the cubic system:simple cubic , body centred cubic and face centred cubic, then the ratio of radii of the spheres in these systems will be repsectively,
A.
For simple cubic,
a = 2r
r = a/2
For body centred cubic,
Hence, the ratio of radii in simple cubic, body centred cubic and face centred cubic is
Percentage of free space in a body centred cubic unit cell is
30%
32%
34%
28%
B.
32%
Packing fraction
With which one of the following elements silicon should be doped so as to give p - type of semiconductor?
Germanium
Arsenic
Selenium
Boron
D.
Boron
The n- type semiconductors are obtained when Si or Ge are doped with elements of group 15, eg, Arenic (As), while p-type semiconductors are obtained when Si or GGe are doped with traces of elements of group 13, ie indium (In), Boron (B).
The fraction of totoal volume occupied by the atoms present in a simple cube is:
π/6
π /4
A.
π/6
For simple cubic
If NaCl is doped with 10-4 mol% of SrCl2 the concentration of cation vacancies will be
(NA = 6.02 x 1023 mol-1):
6.02 x 1015 mol-1
6.02 x 1016 mol-1
6.02 x 1017
6.02 x 1014
A.
6.02 x 1015 mol-1
If NaCl is doped with 10-4 mol% of SrCl2,
2 Na+ ions doped by Sr2+ NA = 6.02 x 1023
The concentration of cation vacancies
= 6.02 x 1023 x10-8
= 6.02 x 1015 mol-1
The appearance of colour is solid alkali metal halides is generally due to:
F- centres
Schottky defect
Frenkel defect
interstitial positions
A.
F- centres
The appearance of colour in solid alkali metal halides is generally due to F-centres.
Which is the incorrect statement?
FeO0.98 has non stoichiometric metal deficiency defect
Density decreases in case of crystals with Schottky's defect
NaCl(s) is insulator, silicon is semiconductor,silver is conductor, quartz is piezo electric crystal
Frenkel defect is favoured in those ionic compounds in which sizes of cation and anionsare almost equal
A.
FeO0.98 has non stoichiometric metal deficiency defect
D.
Frenkel defect is favoured in those ionic compounds in which sizes of cation and anionsare almost equal
Frenkel defect occurs in those ionic compounds in which size of cation and anion is largely different.
The non-stoichiometric ferrous oxide is Fe0.93–0.96O1.00 and it is due to metal deficiency defect.
Iron exhibits bcc structure at room temperature. Above 900°C, it transforms to fcc structure. The ratio of density of iron at room temperature to that at 900°C (assuming molar mass and atomic radii of iron remains constant with temperature) is
1/2
D.
For bcc lattice: Z = 2, a =
For fcc lattice: Z = 4, a =
A solid AB has a NaCl structure. If the radius of cation A+ is 170 pm, then the maximum possible radius of the anion B- is
397.4 pm
347.9 pm
210.9 pm
410.6 pm
D.
410.6 pm
For NaCl type structure,
For maximum possible radium of B-
Sponsor Area
Sponsor Area