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Chapter 1 Solid State

The document discusses various concepts related to solid-state chemistry, including defects in crystal lattices, types of solids, and relationships between atomic radius and unit cell dimensions. It covers topics such as isomorphism, polymorphism, packing efficiency, and magnetic properties of materials. Additionally, it provides calculations and examples related to density, molar mass, and unit cell structure.

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0% found this document useful (0 votes)
27 views7 pages

Chapter 1 Solid State

The document discusses various concepts related to solid-state chemistry, including defects in crystal lattices, types of solids, and relationships between atomic radius and unit cell dimensions. It covers topics such as isomorphism, polymorphism, packing efficiency, and magnetic properties of materials. Additionally, it provides calculations and examples related to density, molar mass, and unit cell structure.

Uploaded by

ttaannmmaayy11
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Chapter 1: Solid State

Very Short Answer Questions (1 Mark)

1. Effect on density in Frenkel defect:

o Frenkel defect does not affect the density of a solid because the ions remain within
the lattice structure, only relocating to interstitial sites.

2. Example of a diamagnetic substance:

o A common example of a diamagnetic substance is sodium chloride (NaCl).


Diamagnetic materials have all their electrons paired, leading to no net magnetic
moment.

3. Common property of hcp and ccp crystal lattices:

o Both hcp (hexagonal close-packed) and ccp (cubic close-packed) lattices have a
packing efficiency of 74% and coordination number 12.

4. Relationship between radius of atom (r) and edge length (a) in fcc unit cell:

o In a face-centered cubic (fcc) unit cell, the relationship is: a=22ra = 2\sqrt{2}r where
"a" is the edge length and "r" is the atomic radius.

5. Diagram of bcc unit cell:

o A body-centered cubic (bcc) unit cell has atoms at the eight corners of the cube and
one atom at the center. (Illustration needed)

6. Number of tetrahedral voids for N/2 atoms:

o The number of tetrahedral voids is equal to twice the number of atoms in the
crystal. For N/2 atoms, there will be N tetrahedral voids.

7. Percentage of empty space in bcc lattice:

o Packing efficiency of a bcc lattice is approximately 68%, so the percentage of empty


space is: 100−68=32%100 - 68 = 32\%

8. Volume occupied by particles in simple cubic unit cell with total volume 6.817 × 10⁻²³ cm³:

o Packing efficiency of a simple cubic lattice is 52.4%. The volume occupied by


particles is: 6.817×10−23×0.524=3.57×10−23 cm36.817 × 10⁻²³ × 0.524 = 3.57 × 10⁻²³
\text{ cm}³

9. Number of octahedral voids in 0.5 mol of hcp structure compound:

o In an hcp structure, the number of octahedral voids equals the number of atoms.
For 0.5 mol of atoms: Number of voids=0.5×6.022×1023=3.011×1023\text{Number
of voids} = 0.5 \times 6.022 \times 10²³ = 3.011 \times 10²³

10. Number of atoms in fcc unit cell:

o In a face-centered cubic unit cell, the total number of atoms is:


8×18+6×12=4 atoms per unit cell.8 \times \frac{1}{8} + 6 \times \frac{1}{2} = 4 \
text{ atoms per unit cell.}
Short Answer Questions (Type I) (2 Marks)

1. Isomorphism and Polymorphism with examples:

o Isomorphism: Substances with similar chemical composition but different crystalline


structures are called isomorphs. An example is Potassium Nitrate (KNO₃) and Sodium
Nitrate (NaNO₃), both of which exhibit similar crystal structures.

o Polymorphism: Polymorphism refers to a single compound existing in more than


one crystalline form. An example is Carbon, which can exist as Diamond (tetrahedral
structure) and Graphite (layered structure).

2. Classification of solids:

o Molecular solids: These consist of molecules as constituent particles. Example: SO₂,


where intermolecular forces hold the molecules together.

o Ionic solids: These consist of cations and anions held together by strong electrostatic
forces. Example: MgF₂.

o Covalent solids: These consist of atoms interconnected by covalent bonds. Example:


Quartz (SiO₂).

o Metallic solids: These consist of metal atoms held together by a "sea of electrons."
Example: Lead (Pb).

3. Vacancy defect with diagram:

o Explanation: A vacancy defect occurs when some lattice points in a crystal remain
unoccupied. This reduces the density of the substance because fewer atoms occupy
the crystal lattice than theoretically expected.

o Diagram: A regular lattice structure with a few missing atoms at specific lattice
points.

4. Number of unit cells in 0.3 g species with density 8.5 g/cm³ and edge length 3.25 × 10⁻⁸
cm:

o Step 1: Calculate the volume of a unit cell: a3=(3.25×10−8)3=3.45×10−23 cm3a^3 =


(3.25 \times 10⁻⁸)^3 = 3.45 \times 10⁻²³ \text{ cm}³

o Step 2: Calculate the mass of one unit cell:


Mass of unit cell=Density×Volume=8.5×3.45×10−23=2.93×10−22 g\text{Mass of unit
cell} = \text{Density} \times \text{Volume} = 8.5 \times 3.45 \times 10⁻²³ = 2.93 \
times 10⁻²² \text{ g}

o Step 3: Calculate the number of unit cells:


Number of unit cells=Total massMass of one unit cell=0.32.93×10−22=1.02×1021\
text{Number of unit cells} = \frac{\text{Total mass}}{\text{Mass of one unit cell}} = \
frac{0.3}{2.93 \times 10⁻²²} = 1.02 \times 10²¹

5. Unit cell edge length for bcc structure with atom diameter 120 pm:
o Step 1: Calculate the radius of the atom: r=Diameter2=1202=60 pmr = \frac{\
text{Diameter}}{2} = \frac{120}{2} = 60 \text{ pm}

o Step 2: For a bcc lattice, the relationship between edge length aa and radius rr is:
a=4r3a = \frac{4r}{\sqrt{3}} Substituting: a=4×601.732=138.6 pma = \frac{4 \times
60}{1.732} = 138.6 \text{ pm}

6. Difference between crystalline and amorphous solids:

o Crystalline Solids:

 Structure: Regular and ordered arrangement of particles.

 Melting Point: Sharp and well-defined.

 Examples: NaCl, Diamond.

o Amorphous Solids:

 Structure: Irregular and disordered arrangement of particles.

 Melting Point: Over a range of temperatures.

 Examples: Glass, Rubber.

7. Density of gold with fcc structure (edge length 408 pm, molar mass 197 g/mol):

o Step 1: Use the formula: ρ=Z×Ma3×NA\rho = \frac{Z \times M}{a^3 \times N_A}
where Z=4Z = 4, M=197 g/molM = 197 \text{ g/mol}, a=408×10−8 cma = 408 \times
10⁻⁸ \text{ cm}, NA=6.022×1023N_A = 6.022 \times 10²³.

o Step 2: Substituting values: ρ=4×197(408×10−8)3×6.022×1023\rho = \frac{4 \times


197}{(408 \times 10⁻⁸)^3 \times 6.022 \times 10²³}

 Calculate: ρ=19.27 g/cm3\rho = 19.27 \text{ g/cm}³

8. Substitutional and interstitial impurity defects:

o Substitutional defect:

 Explanation: Foreign atoms replace some host atoms in the lattice. Example:
In Brass, Zinc atoms replace Copper atoms.

o Interstitial defect:

 Explanation: Smaller atoms occupy voids between host atoms. Example:


Carbon atoms in the iron lattice in steel.

Short Answer Questions (Type II) (3 Marks)

1. Packing efficiency of bcc lattice:

o The packing efficiency is the fraction of the total volume of a unit cell that is
occupied by atoms. For a bcc lattice:
 Step 1: Volume of one atom: Volume of one atom=43πr3\text{Volume of
one atom} = \frac{4}{3} \pi r^3

 Step 2: Total volume occupied by 2 atoms in a bcc unit cell:


Volume of 2 atoms=2×43πr3\text{Volume of 2 atoms} = 2 \times \frac{4}
{3} \pi r^3

 Step 3: Packing efficiency:


Packing efficiency=Volume occupied by atomsVolume of unit cell×100\
text{Packing efficiency} = \frac{\text{Volume occupied by atoms}}{\
text{Volume of unit cell}} \times 100 Substituting a=4r3a = \frac{4r}{\
sqrt{3}}, the packing efficiency is calculated to be approximately 68%.

2. Arrangement of spheres in hcp structure:

o In an hcp structure:

 First Layer: The spheres are arranged in a hexagonal pattern.

 Second Layer: The spheres fit into the triangular depressions of the first
layer.

 Third Layer: The spheres align directly above the first layer, forming an
ABAB stacking pattern.

 This arrangement ensures high packing efficiency of 74%, and the


coordination number of each sphere is 12.

3. Molar mass from density (density = 21.5 g/cm³, fcc structure, edge length 367.8 pm):

o Step 1: Use the formula: M=ρ×a3×NAZM = \frac{\rho \times a^3 \times N_A}{Z}

o Step 2: Convert edge length to cm: a=367.8×10−8 cma = 367.8 \times 10^{-8} \
text{ cm}

o Step 3: Substituting values: M=21.5×(367.8×10−8)3×6.022×10234M = \frac{21.5 \


times (367.8 \times 10^{-8})^3 \times 6.022 \times 10^{23}}{4}

o Step 4: Simplify: M=161.1 g/molM = 161.1 \text{ g/mol}

o Conclusion: The molar mass of the element is 161.1 g/mol, consistent with its
calculated density and structure.

4. Radius of Na atom (bcc, density = 0.97 g/cm³, molar mass = 23 g/mol):

o Step 1: Use the density formula: ρ=Z×Ma3×NA\rho = \frac{Z \times M}{a^3 \times
N_A}

o Step 2: Rearrange to find edge length aa: a3=Z×Mρ×NAa^3 = \frac{Z \times M}{\
rho \times N_A} Substituting values: a3=2×230.97×6.022×1023a^3 = \frac{2 \times
23}{0.97 \times 6.022 \times 10^{23}} a=4.29×10−8 cma = 4.29 \times 10^{-8} \
text{ cm}

o Step 3: For bcc, a=4r3a = \frac{4r}{\sqrt{3}}, solve for rr: r=a×34=4.29×10−8×1.7324r


= \frac{a \times \sqrt{3}}{4} = \frac{4.29 \times 10^{-8} \times 1.732}{4}
r=1.86×10−8 cmr = 1.86 \times 10^{-8} \text{ cm}
o Conclusion: The radius of the sodium atom is approximately 1.86 × 10⁻⁸ cm.

5. Classification of non-stoichiometric defects with metal deficiency defect diagram:

o Non-stoichiometric defects:

 These defects occur when the ratio of cations to anions deviates from the
ideal stoichiometric ratio.

 Types:

1. Metal excess defect: Caused by extra cations or interstitial


electrons. Example: ZnO (appears yellow due to excess zinc ions).

2. Metal deficiency defect: Caused by missing cations, balanced by


higher oxidation states of nearby cations. Example: FeO.

o Diagram: A lattice diagram showing a missing Fe²⁺ ion replaced by two Fe³⁺ ions to
maintain charge neutrality.

6. Diamagnetic, paramagnetic, ferromagnetic examples:

o Diamagnetic: Materials with paired electrons that are repelled by a magnetic field.
Example: NaCl.

o Paramagnetic: Materials with unpaired electrons that are weakly attracted to a


magnetic field. Example: O₂.

o Ferromagnetic: Materials with domains that align strongly in a magnetic field.


Example: Fe (Iron).

7. Relation between edge length (a) and radius (r):

o Simple cubic: a=2ra = 2r

o Body-centered cubic (bcc): a=4r3a = \frac{4r}{\sqrt{3}}

o Face-centered cubic (fcc): a=22ra = 2\sqrt{2}r

o These relationships are derived from geometric considerations of how atoms are
arranged within the unit cell.

8. Definitions:

o Diamagnetic solids: Substances with paired electrons repelled by magnetic fields.

o Paramagnetic solids: Substances with unpaired electrons attracted by magnetic


fields.

o Ferromagnetic solids: Substances exhibiting strong magnetization due to domain


alignment (e.g., Fe).

Long Answer Questions (4 Marks)

1. Non-stoichiometric defects and F-center formation:


o Definition: Non-stoichiometric defects occur when the stoichiometry of a compound
is not maintained due to missing or excess atoms or ions.

o F-centers: F-centers, or color centers, are a specific type of non-stoichiometric


defect. They form when an anion vacancy is occupied by an electron. This electron
absorbs visible light, imparting color to the crystal. For example, in NaCl, the
presence of F-centers causes the crystal to appear yellow.

o Significance: F-centers are important as they affect the optical and electrical
properties of materials and are widely studied in solid-state physics.

2. Classification of stoichiometric defects with substitutional impurity defect explanation:

o Stoichiometric defects:

1. Vacancy defect: Some lattice sites are vacant, reducing the density of the
substance. Example: NaCl.

2. Interstitial defect: Atoms occupy interstitial sites in the crystal. Example: Fe


in steel.

o Substitutional impurity defect:

 In substitutional defects, foreign atoms replace host atoms in the lattice. For
instance, in brass, zinc atoms replace some of the copper atoms.

 Effect: These defects can alter the electrical, thermal, and mechanical
properties of the material.

3. Density, molar mass, and unit cell edge length relationship:

o The density of a unit cell is given by: ρ=Z×Ma3×NA\rho = \frac{Z \times M}{a^3 \
times N_A} where ρ\rho is the density, ZZ is the number of atoms per unit cell, MM
is the molar mass, aa is the edge length of the unit cell, and NAN_A is Avogadro's
number.

o Derivation: Using this formula, the number of particles and unit cells in a given mass
of metal can be calculated by rearranging for ZZ or aa.

o Applications: This formula is used in determining unknown densities or molar


masses of crystalline solids.

4. Bravais lattices definition and niobium bcc calculation:

o Definition: Bravais lattices are 14 distinct 3D arrangements of points that describe all
possible crystal structures. Examples include cubic, tetragonal, orthorhombic, etc.

o Calculation for niobium:

 Given density = 8.55 g/cm³, edge length = 330.6 pm.

 Using the formula ρ=Z×Ma3×NA\rho = \frac{Z \times M}{a^3 \times N_A},


calculate the number of atoms and unit cells:

 Number of atoms: 3.237×10213.237 \times 10^{21}.


 Number of unit cells: 1.618×10211.618 \times 10^{21}.

5. Definitions:

o Conductors: Materials that allow the flow of electric current. Example: Copper (Cu).

o Insulators: Materials that block the flow of electric current. Example: Glass.

o Semiconductors: Materials with conductivity between that of conductors and


insulators. Example: Silicon (Si).

o Doping: The process of adding impurities to semiconductors to improve their


electrical conductivity. Example: Adding phosphorus to silicon.

Next: Chapter 2: Solutions.

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