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Metallic Bond

Pre-requisite: Nuclear charge, Valence electrons

Stovetop cooking routinely requires cast iron or aluminium pans but never a glass pan or a pan made of silicon. That’s because the glass pan will shatter at high temperatures, and the silicon pan will burn away.

On the other hand, iron or aluminium pans and metal alloys like steel can withstand and conduct high heat. In addition to heat, such metals can conduct electricity - for example, copper metals in electric wires and tungsten filament in lamps. 

Properties of metals

Each metal has a unique nature - Iron and Aluminium are hard, but Sodium, Mercury, and Gold are soft. Their special nature allows the metals to be moulded into shapes, beaten into sheets, and drawn into wires like in gold jewellery.

Metals have shine, some are heavy, and few in an alloy form display excellent strength to bear the load and not fracture under stress. Therefore, they find wide applications in building bridges, railroads, cranes, etc.

Charachteristics of metallic solid

The properties that make metals so unique lie in how the atoms inside the metal are bonded.

What is Metallic Bonding?

Metallic bonding is the electrostatic force holding a vast collection of metal atoms in a solid structure.

In metals, the atom's size is huge such that the atom's nucleus cannot firmly hold the outermost valence electrons by attraction. The electrons escape from the nuclear hold and drift.

 

 

Nuclear charge unable to hold metal atom's valence electrons

The atom becomes a positively charged kernel on losing its electron. These kernels are spaced at equal distances to avoid repulsion, looking like lattices, and holding the solid structure.

The lost electrons flow through these positive lattices due to electrostatic attraction so that the electrical neutrality of the structure is maintained, like a sea floating around the kernel islands. 

what is a metallic bond

 

Kernels are not ions, as the lost electrons are always replaced in the desired number by the other floating electrons from the nearby atoms. The kernel-valence electrons' relationship is of attraction that does not require a tight binding to an individual atom.

 

 

what electrons flow in a metallic bond

 

The metals ability to easily ionize or lose its electrons is due to its low ionization potential. Also, the metals prefer to undergo electron loss to obtain the stable electronic configuration of the nearest inert gas.

Importance of Metallic Bonding

The non-fixated kernel-electron attractive bonding allows the layers of metal atoms to slide past one another and get reorganized without losing identity.

The readjustment allows the metal atoms to merge between layers or to spread into wires, largely contributing to the malleability and ductility.

The free-electron movement also discourages the positively charged kernels from coming too close and showing repulsion, thereby balancing the positive and negatively charged metal structure. 

How is metallic bonding different from ionic bonding?

The ionic compounds are formed when metals lose their electrons and nonmetals gain to form ions. However, in ionic compounds, the ions are held in fixed geometry, and in the solid state, the ions are immobile. 

Also, the ionic compounds do not show a metal’s unique property of layers sliding past each other.

Ionic bond versus vs Metallic Bond

What is the impact of metallic bonding on the physical properties?

Metals with more valence electrons will have greater mobile electrons, which will raise a metal's conductivity to heat and electricity.

Also, when a metal employs a larger set of electrons for delocalization, subsequent nuclear charge increases, raising the kernel-electron attractive power. The higher kernel-electron attractive strength raises the physical properties of the melting and the boiling point. 

For example, Na metal has one valence electron, and Al has three valence electrons. Na can lose one electron to give Nakernel and one free e-. By losing the electron, the nuclear charge of Na is +1. If Al loses its three mobile electrons (e-) to form the Al3+ kernel, it will have a nuclear charge of +3.

The higher the nuclear charge, the higher the kernel-electron attractive power will be. Therefore, Al3+ will show higher attractive strength for the mobile electrons than the Na+ kernel raising the melting and the boiling point.   

ElementMelting PointBoiling pointValence Electrons
Sodium97.79 oC882.9 oC1
Aluminium660 oC2470 oC3

The transition metals with greater free electrons in the 3d and 4s orbitals than s-block or p-block metals will show higher melting and boiling points. 

ElementMelting Point (oC)Boiling Point (oC)Valence electrons
Sodium (s-block)97.79882.91
Magnesium (p-block)650

 

1091

 

2
Aluminium (p-block)66024703
Iron (transition, d-block)120427508
Nickel (transition, d-block)1453273210

Increase in Valence e increases M.P., and B.P.

Note that the melting points are lower than the boiling points as a metal's bonds are only loosened on melting. However, boiling a metal requires higher energy input,  breaking the kernel-electron attractive force and truly destroying the crystal structure.

What are the applications of metallic bonding?

The property of metallic bonding is harnessed for thermal, electrical conductivities, lustre, and shape. Also, mixing different metals forms alloys with new separate improved identities that display greater potential and have broader applications.

For example, steel, an alloy of iron and carbon, is harder than iron itself.

An alloy of Nickle and titanium is called nitinol, responsible for shape memory and capable of springing back to shape and displaying superelasticity at different temperatures. 

The science of metallic bonding is also used to tweak the crystal structure of semiconductors (Si, Ge, etc.) to introduce n-type (negative type) or p-type (positive type) defects. The defect dramatically improves the semiconductor's processing power and performance, which finds broader applications in transistors, diodes, circuits, computers, cars, and smartphones. 


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About the chapter - Bonding in Atoms

Octet Rule determines Ionic and Covalent Bonds. The chapter offers in-depth coverage of the rule and demonstrates how to assess bonding in atoms by analyzing the nature, formation, requirement, types, number, and other bond-related properties. The chapter ends with metallic bonding, its nature, significance, and application, with a complete overview of the difference between various bond types.

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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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