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Classification of Solids, Structure, and Order

Types of Solids- Crystalline and Amorphous

Solids are made up of many particles, and depending on how they are arranged, solids can be divided into crystalline solids and amorphous solids.

The particles may be atoms, ions, or molecules. 
For example, gold atoms, NaCl ions, and sucrose molecules compose the solid-state. 

 

properties of matter classification of solids

Formation and arrangement of solid particles

Suppose a solid is heated to a particularly high temperature, and the molten liquid is gradually cooled. In that case, the constituent particles get sufficient time to arrange themselves into a highly ordered crystalline solid structure, a process called annealing. Annealing effects the crystalline properties of the solid and is sometimes used to rearrange the particles until they reach the crystalline state.

Examples of crystalline solids are Diamond, NaCl, and Quartz.

However, instead of gradually cooling, if the molten liquid is cooled rapidly or if the liquid vapors are frozen suddenly, the particles do not get enough time to organize efficiently. The arrangement of particles is disordered, and the resulting solid is called an amorphous solid.

Examples of amorphous solids are Rubber, Glass, Tar, Plastic, and Quartz glass.

However, the notion of a perfect crystalline solid is false. One can obtain an ideal, perfect crystalline solid at 0K, a very low temperature at which the particles do not have any thermal energy. Therefore, they have no motion; there is no disorder leading to zero entropy. At this temperature, the particles can arrange themselves in perfect order. At all other temperatures, minor irregularities always exist in the crystal structure, and an ideal crystalline solid is not obtained.

Crystalline solid structure

The smallest building block of a crystal is called a unit cell. On the corners of the unit cell, the particles of the solid occupy their positions.

 In addition to the corners, some atoms may also be present at the center, on the faces, or at the edges of the unit cell. These places that atoms occupy in a unit cell are called the lattice points.

crystalline solid structure

Many such unit cells repeat to give a complete crystalline lattice. It is called a lattice because, in the two dimensions, a crystal looks like a series of points with criss-cross lines like a network or mesh. 

lattice points in 2D crystalline solid state

When the entire crystal is shown as lines and points in the three dimensions, it's called a crystal lattice. As the unit cells extend in all three dimensions in space, a crystal lattice is also known as a space lattice. These repeating structures of the unit cell in all three dimensions give an entire crystalline solid. 

crystal lattice space lattice extensive arrangement

Therefore, by maintaining the order of the arrangement of the unit cells and their periodic repetition, an entire crystalline solid is obtained.

One way to understand is by comparing the crystalline solid with a human body. The human cell is the basic unit of all the living organisms, like the unit cell is a crystalline solid. The biological cells unite to form a multi-cellular organism. Similarly, many unit cells combine in the three dimensions to give a crystalline solid.

Order of particles in Crystalline solids

Crystalline solids have both short-range and long-range order, which means that the constituent particle arrangement is ordered and regularly repeated in smaller and extended regions. Therefore, one can predict the structure of the entire crystal if the structure of only one unit cell is known.

Amorphous solid structure

The amorphous solid has a tightly packed, random arrangement of the constituent particles. The amorphous solids have no unit cell or periodic, repetitive arrangement of cells. The angles and the lengths between the particles differ.

Order particles in Amorphous solids

Due to their random arrangement of the particles, amorphous solids do not have any long-range order but may have short-range order

It means that there may exist small, scattered regions in the amorphous solids, which may have an ordered arrangement of the constituent particles as seen in the crystalline solids. Such crystals that are part of an amorphous solid are called crystallites.


Course on Introductory Organic Chemistry 



Introductory Organic Chemistry Course covers the fundamentals of organic chemistry in 13 detailed chapters –

  • Atoms

  • Bonding in Atoms

  • Covalent Bond 

  • Electronic Displacements in a Covalent Bond 

  • Common Reaction Types 

  • Drawing Organic Structures 

  • Functional Groups 

  • Structural Isomerism 

  • Intermolecular Forces 

  • Physical Properties 

  • Fundamentals of Organic Reactions 

  • Reactive Intermediates 

The course simplifies the language of Organic Chemistry with pictures, metaphors, and common words that anyone can understand.

It is a detailed, handy primer for building a strong foundation in Organic Chemistry.

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What is Organic Chemistry?

  • Introduction
  • Elements of a Chemical Reaction
  • Components of a Chemical Reaction

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Atom

  • Size of an atom- The world belongs to the tiniest!
  • Power of Protons
  • Mass Number
  • Average Atomic Mass
  • Molecule and Molecular Mass
  • The Electrons- An Atom’s Reactive Component
  • Atomic Orbitals- s, p, d, f
  • Filing of Atomic Orbitals and Writing Electronic Configuration
  • Valence and Core Electrons- How to Determine

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Bonding In Atoms

  • Octet Rule- Introduction and Bonding
  • Limitations of Octet Rule
  • Ionic Bond- Introduction and Formation
  • Formation of Ionic Compound
  • Requirements for Ionic Bonding
  • Appearance and Nature of Ionic Compounds
  • Physical Properties of Ionic Solids- Conductance, Solubility, Melting Point, and Boiling Point
  • Covalent Bond - How it Forms
  • Covalent Bond - Why it Forms?
  • Covalent Bond- Bond Pair (Single, Double, Triple) and Lone Pair
  • Number of Covalent Bonds- Valency
  • Types of Covalent Bonds- Polar and Nonpolar
  • Metallic Bonds- Introduction and Nature
  • Significance of Metallic Bonding
  • Impact of Metallic Bonding on the Physical Properties
  • Applications of Metallic Bonding
  • Difference Between Metallic and Ionic Bond

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Covalent Bond

  • Theories on Covalent Bond Formation
  • Valence Bond Theory- Introduction and Covalent Bond Formation
  • Valence Bond Theory- Types of Orbital Overlap Forming Covalent Bonds
  • Applications, Limitations, and Extensions of Valence Bond Theory
  • Hybridization- Introduction and Types
  • sp3 Hybridization of Carbon, Nitrogen, and Oxygen
  • sp2 Hybridization of Carbon, Carbocation, Nitrogen, and Oxygen
  • sp Hybridization of Carbon and Nitrogen
  • Shortcut to Determine Hybridization
  • VSEPR Theory- Introduction
  • Difference between Electron Pair Geometry and Molecular Structure
  • Finding Electron Pair Geometry and Related Shape
  • Predicting Electron-Pair Geometry and Molecular Structure Guideline
  • Predicting Electron pair geometry and Molecular structure - Examples
  • Finding Electron-Pair Geometry and Shape in Multicentre Molecules
  • Drawbacks of VSEPR Theory
  • Covalent bond Characteristics- Bond length
  • Factors affecting Bond Length
  • How does Electron delocalization (Resonance) affect the Bond length?
  • Covalent bond Characteristics- Bond Angle
  • Factors affecting Bond Angle
  • Covalent bond Characteristics- Bond Order
  • How Bond Order Corresponds to the Bond Strength and Bond Length
  • Solved Examples of Bond Order Calculations
  • Covalent Bond Rotation
  • Covalent Bond Breakage
  • Covalent Bond Properties -Physical State, Melting and Boiling Points, Electrical Conductivity, Solubility, Isomerism, Non-ionic Reactions Rate, Crystal structure

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Electronic Displacement in a Covalent Bond

  • Electronegativity- Introduction
  • Factors Affecting Electronegativity- Atomic number, Atomic size, Shielding effect
  • Factors Affecting Electronegativity-s-orbitals, Oxidation state, Group electronegativity
  • Application of Electronegativity in Organic Chemistry
  • Physical Properties Affected by Electronegativity
  • Inductive effect- Introduction, Types, Classification, and Representation
  • Factors Affecting Inductive Effect- Electronegativity
  • Factors Affecting Inductive Effect- Bonding Order and Charge
  • Factors Affecting Inductive Effect- Bonding Position 
  • Application of Inductive Effect- Acidity Enhancement and Stabilization of the counter ion due to -I effect 
  • Application of Inductive Effect-Basicity enhancement and stabilization of the counter ion due to +I effect
  • Application of Inductive Effect-Stability of the Transition States
  • Application of Inductive Effect-Elevated Physical Properties of Polar Compounds
  • Is the Inductive Effect the same as Electronegativity?
  • Resonance- Introduction and Electron Delocalization 
  • Partial Double Bond Character and Resonance Hybrid
  • Resonance Energy
  • Significance of Planarity and Conjugation in Resonance
  • p-orbital Electron Delocalization in Resonance
  • Sigma Electron Delocalization (Hyperconjugation)
  • Significance of Hyperconjugation
  • Resonance Effect and Types
  • Structure Drawing Rules of Resonance (Includes Summary)
  • Application of Resonance
  • Introduction to Covalent Bond Polarity and Dipole Moment
  • Molecular Dipole Moment
  • Lone Pair in Molecular Dipole Moment
  • Applications of Dipole Moment
  • Formal Charges- Introduction and Basics
  • How to Calculate Formal Charges (With Solved Examples)
  • Difference between Formal charges and Oxidation State

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Common Types of Reactions

  • Classification of common reactions based on mechanisms
  • Addition Reactions
  • Elimination Reactions (E1, E2, E1cb)
  • Substitutions (SN1, SN2, SNAr, Electrophilic, Nucleophilic)
  • Decomposition
  • Rearrangement
  • Oxidation-Reduction

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Drawing Organic Structures

  • Introduction
  • Kekulé
  • Condensed
  • Skeletal or Bond line
  • Polygon formula
  • Lewis Structures- What are Lewis structures and How to Draw
  • Rules to Draw Lewis structures- With Solved Examples
  • Lewis structures- Solved Examples, Neutral molecules, Anions, and Cations
  • Limitation of Lewis structures
  • 3D structure representation- Dash and Wedge line
  • Molecular models for organic structure representation- Stick model, Ball-stick, and Space-filling
  • Molecular Formula

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Functional Groups in Organic Chemistry

  • What are functional groups? 
  • Chemical and Physical Properties affected by the Functional Groups
  • Identifying Functional Groups by name and structure
  • Functional Group Categorization- Exclusively Carbon-containing Functional Groups
  • Functional Group Categorization- Functional Groups with Carbon-Heteroatom Single Bond
  • Functional Group Categorization- Functional Groups with Carbon-Heteroatom Multiple Bonds
  • Rules for IUPAC nomenclature of Polyfunctional Compounds
  • Examples of polyfunctional compounds named according to the priority order
  • Examples of reactions wherein the functional group undergoes transformations

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Structural Isomerism

  • Introduction
  • Chain Isomerism
  • Position Isomerism
  • Functional Isomerism
  • Tautomerism
  • Metamerism
  • Ring-Chain Isomerism

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Intermolecular Forces

  • Ion-Dipole Interactions-Introduction and Occurrence
  • Factors Affecting the Ion-Dipole Strength
  • Importance of Ion-Dipole Interactions
  • Ion-Induced Dipole- Introduction, Strength and Occurrence
  • Factors Affecting the Strength of Ion-Induced Dipole Interactions
  • Ion-Induce Dipole Interactions in Polar Molecules
  • Vander Waals Forces -Introduction
  • Examples of Vander Waals' forces
  • Vander Waals Debye (Polar-Nonpolar) Interactions
  • Factors affecting the Strength of Debye Forces
  • Vander Waals Keesom Force- Introduction, Occurrence and Strength
  • Vander Waals London Forces- Introduction, Occurrence, And Importance
  • Factors Affecting the Strength of London Dispersion Forces- Atomic size and Shape
  • Introduction, Occurrence and Donor, Acceptors of Hydrogen Bond
  • Hydrogen bond Strength, Significance and Types
  • Factors Affecting Hydrogen Bond Strength
  • Impact of Hydrogen bonding on Physical Properties- Melting and boiling point, Solubility, and State
  • Calculation of the Number of Hydrogen Bonds and Hydrogen bond Detection

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Physical Properties

  • Physical Properties- Introduction, Role of Intermolecular Forces
  • Physical State Change-Melting Point
  • Role of Symmetry, Role of Carbon numbers, Role of Geometry
  • Physical State Change-Boiling Point
  • Intermolecular Forces and their Effect on the Boiling Point, Role of Molecular Weight (Size), Molecular Shape, Polarity
  • Boiling Point of Special Compounds- Amino acids, Carbohydrates, Fluoro compounds
  • Solubility in Water
  • Density

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Fundamentals of Organic Reactions

  • Types of Arrows Used in Chemistry
  • Curved Arrows in Organic Chemistry- with Examples
  • Electrophiles- Introduction, Identification and Reaction
  • Formation and Classification of Electrophiles- Neutral and Charged 
  • Difference between Electrophiles and Lewis Acids
  • Nucleophile- Identification and Role in a Reaction
  • Types of Nucleophiles- Lone Pair
  • Types of Nucleophiles- Pie Bond
  • Types of Nucleophiles- Sigma Bond
  • Periodic Trend and Order in Nucleophilicity
  • Introduction to Reactions Involving Nucleophiles
  • Nucleophile Reactions- Aliphatic Displacement type - SN1, SN2
  • Nucleophile Reactions- Acyl Displacement type
  • Nucleophile reactions- Aromatic Displacement type- Electrophilic, Nucleophilic
  • Addition Reactions- Electrophilic, Nucleophilic, and Acyl
  • Ambident Nucleophiles- Introduction and Formation 
  • Ambident Nucleophile - Nature of the Substrate
  • Ambident Nucleophile- Influence of the Positive Counter Ions
  • Ambident Nucleophile- Effect of Solvent 
  • Lone Pair - Introduction and Formation
  • Physical Properties Affected by the Lone Pair- Shape and Bond Angle
  • Physical Properties Affected by the Lone Pair- Hydrogen Bonding
  • Physical Properties Affected by the Lone Pair- Polarity and Dipole Moment
  • Chemical property affected by the Lone pair- Nucleophilicity
  • Leaving Group- Introduction and Nature
  • Good and Bad Leaving Group
  • Factors Determining Stability of the Leaving Groups- Electronegativity, Size, Resonance Stability
  • Using pKa as a Measure of Leaving Group Ability
  • Leaving Groups in Displacement Reactions
  • Leaving Groups in Elimination Reactions

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Reactive Intermediates

  • Carbocation- Introduction, Nature, and Types
  • Formation of Carbocation
  • Stability of Carbocations- Inductive, Resonance, and Hyperconjugation
  • Other Structural Features Increasing Carbocation Stability
  • Structural Feature Decreasing Carbocation Stability
  • Fate of the Carbocation
  • General Carbocation Formation Reactions
  • Carbanion- Introduction, Nature, and Types
  • Formation of Carbanions
  • Carbanion Stabilization
  • Ease of Formation of Carbanion -Acidic proton
  • Fate of the Carbanion
  • Free Radical- Introduction and Types of Carbon-Centred Radicals
  • Structure of Carbon-Centred Free Radical
  • Formation of Radicals
  • Stability of the Carbon-Centred Radicals
  • Other Structural Feature Increasing Free Radical Stability
  • Comparing Free Radical Stability using Dissociation energies (D-H) 
  • Fate of Free Radicals
  • Common Reactions Involving Carbon-Free Radicals

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