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Why do atoms need to form covalent bonds?

The atoms that embark on the journey of bond formation are likely to have an electron imbalance. They are less stable and become highly reactive. These atoms seek 8 electrons in their outermost shell to lower their reactivity and achieve stability.

Best reason why atoms form covalent bonds

The number 8 as the stable electronic configuration the atoms pursue was formulated by Gilbert N. Lewis in his ‘octet rule.’  According to him, all noble gases (He, Ne, Ar, Kr, Xe, Rn) are stable, and their octet configuration guarantees stability. The exception is Helium which prefers the duplet state.

The inertness of the noble gas atoms under normal conditions is attributed to their complete shell, and therefore, they are unreactive with another atom, preferring sole existence. In comparison, other elements try to attain stability by losing, gaining, or sharing the electrons to reach the electronic configuration of their nearest noble gases.

Why do atoms form bonds

For example, the electronic configuration of Sodium is 11. It must lose one electron to reach the nearest noble gas configuration of Neon or gain seven electrons to reach the configuration of Argon. Sodium prefers to lose one electron rather than gain seven electrons. However, a Chlorine atom with 7 outer electrons in the same row is devoid of one electron from the stable configuration. Instead of losing all 7 electrons to reach the Neon configuration, it prefers to gain one and attain the electronic configuration of Argon.  Losing or gaining many electrons is not an energetically feasible process for an atom.

The other atoms that don’t have too much to lose or gain prefer a middle path -sharing.

An atom’s preference to lose, gain or share electrons determines the type of bond it will form, whether covalent or ionic. Their electronegativity (in addition to ionization and electron gain enthalpy) values control the bonding preference.

Only those elements with an electronegativity difference of 1.7 and higher chose to lose or gain electrons to form ionic bonds.

Most elements below the electronegativity difference value of 1.7 prefer to share the electrons to form molecules with a covalent bond. These elements are usually nonmetals on the periodic table's right side.

For example, a nonmetal carbon forms covalent bonds with other nonmetals, Nitrogen, Oxygen, Hydrogen, and Halogens because these combinations have electronegativity values below 1.7. Therefore, we see many organic carbon compounds with C-C, C-N, C-H, C-O, and C-X covalent linkages.

The sharing of the electrons in a covalent bond mutually benefits the atoms involved. The shared electrons are part of both atoms' nuclei, and they simultaneously fulfill their octet/duplet configuration.

By bonding, the atoms lose their reactivity; the final molecule is lower in energy and more stable than its parents.

For example, an individual H atom with a single electron is high in energy. The atom wants to gain one electron to fulfill its duplet state. When two H atoms share one electron each, both attain the stable duplet configuration of Helium (He) and form one hydrogen (H2) molecule. Other combinations are H atom (less by one) with Cl atom (less by one) to form HCl molecule, C atom (less by four) and four H atoms (each less by one) to form CH4, N atom (less by three) and three H atoms (each less by one) to form NH3.

Why do atoms share electrons in a covalent bond

Nitrogen only required three more electrons to complete its octet, forming three bonds with Hydrogen. The remaining unpaired electron on Nitrogen is called the lone pair. Oxygen requires only two more electrons to form two bonds with Hydrogen to meet its octet requirement. The unused electrons are the Oxygen atom’s lone pair. In the above HCl example, Chlorine has three lone pairs. So, the electrons in the molecule are divided into two parts- bond pairs (electrons involved in bonding) and lone pairs (electrons uninvolved in bonding).

Why do atoms share electrons in a covalent bond

Related Reading: Electronegativity


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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
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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
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  • Applications of Metallic Bonding
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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
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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
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Drawing Organic Structures

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  • Condensed
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  • 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
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  • 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
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Structural Isomerism

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Intermolecular Forces

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  • 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
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  • 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
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Physical Properties

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  • Physical State Change-Boiling Point
  • Intermolecular Forces and their Effect on the Boiling Point, Role of Molecular Weight (Size), Molecular Shape, Polarity
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  • 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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