Skip to main content

Vander Waals Debye (Polar-Nonpolar) interactions

Debye, a subtype of Vander Waal's force, is an interaction between polar-nonpolar atoms or molecules.

An example is an interaction between a polar molecule like H-Cl and a neutral, nonpolar atom like Helium.

How it Debye interactions occurs?

Chlorine, the most electronegative atom in HCl, pulls and hoards the bond electron density. The Cl end develops a partial negative charge (denoted as δ-) and becomes the negative terminal, whereas the Hydrogen is positive (denoted as δ+). Therefore, the HCl molecule has two in-built polar ends or a dipole due to Chlorine's electronegativity.

The dipole of HCl will induce pole formation in a neutral He atom when brought to its vicinity. The Helium atom's side closest to the Chlorine will develop an opposite positive charge; consequently, the other end will get a negative charge. Due to the induced polarity, they begin to attract. 

 

What are dipole-induced dipole interactions?

Polar HCl's impact on neutral Helium atoms can be visualized using a magnet and a nail. The magnet has natural north and south poles capable of inducing polarity in the ordinary iron nail.

In the magnet's presence, the iron nails achieve magnetism temporarily and begin to orient. The nails attract each other like the attraction between HCl (as the magnet) and He atom (as iron nails).

example of dipole-induced dipole Vander Waal interaction

Some other examples of polar-nonpolar molecular combinations are HF-H2, HCl-I2, and H2O-Ar. 

Factors affecting the strength of Debye forces

The strength of polar-nonpolar molecular interactions will depend on two factors-

1) electronegativity of the polar molecule, and 

2) polarizability of the neutral, nonpolar atom. 

1) Electronegativity of the polar molecule

The greater the polarity of the polar molecule, the stronger will be the induced polarity and its subsequent interaction with the nonpolar molecule.

For example, comparing the strength of interaction between two polar molecules, HCl and HF, with the nonpolar He atom, it is observed that the Helium atom will interact more strongly with HF than with HCl since Fluorine is more electronegative than Chlorine.

Therefore, electronegativity is the power that will influence the electron cloud of the nonpolar atoms, distorting it and causing greater pole separation.

So, the HF-He pair will have the strongest attractive interaction than the He-HCl pair.

factors affecting dipole-induced dipole interactions

2) Polarizability of the neutral, nonpolar atom

The size of the nonpolar atoms considerably impacts the attractive intermolecular strength.

Bigger atoms have sizable electron clouds that can easily be influenced by nearby polar molecules, causing electron cloud distortion. The distortion allows the formation of poles; therefore, a nonpolar atom's size affects polarizability and increases the attractive strength.

For example, comparing the strength of interaction between HF, smaller Helium (He) atom, and larger Argon (Ar) atom, it is observed that the Argon atom interacts more strongly with HF than the Helium.

size comparison example of induced dipole

The Argon’s electrons being further away from the nucleus, are easily distorted to form temporary poles, resulting in stronger HF-Ar interaction. 

Fewer Helium’s electrons are pulled by the nucleus strongly (nuclear charge), restricting its polarization.

dipole-induced dipole Vander Waals

Therefore, the bigger the atoms' size, the more the electron clouds, and the higher their molecular weight. Such atoms will have greater polarizability, translating to stronger intermolecular attractions.

Such polar-nonpolar interactions are also called the induction effect or dipole-induced dipole interactions.  

Strength of Debye Interaction

The Debye force is stronger than the London force but weaker than the Keesom force.

Keesom force > Debye force > London force

Their other names-

Dipole-Dipole > Dipole-induced dipole > Induced Dipole-Induced Dipole

Orientation effect > Induction Effect > Dispersion effect

comparison of strength Vander Waal forces

Related concepts: Dipole-Dipole Vander Waal interactions, Induced dipole-induced dipole Vander Waal interactions.

 


Get Premium Chemistry Tutorials



About the chapter - Intermolecular Forces

Intermolecular forces determine the strength, properties, and size of atoms. The chapter thoroughly covers some of organic chemistry's most potent intermolecular forces - Ion-dipole, Ion-Induced Dipole, Vander Waals (Debye, Keesom, London), and Hydrogen Bonds.

We also expand on hydrogen bonds, discussing the donor and acceptors of hydrogen bonds, their types, factors affecting hydrogen bond strength, the impact of hydrogen bonding on the physical properties, and ending the chapter with a step-by-step tutorial on calculating the number of hydrogen bonds.

Subscribers Only Premium Tutorials

What is Organic Chemistry?

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

     Get Organic Chemistry

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

     Get Atom

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

     Get Bonding in Atoms

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

     Get Covalent Bond

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

     Get Electronic Displacements in a Covalent Bond

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

     Get Common Types of Reactions

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

     Get Drawing Organic Structures

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

     Get Functional Groups in Organic Chemistry

Structural Isomerism

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

     Get Structural Isomerism

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

     Get Intermolecular Forces

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

     Get Physical Properties

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

     Get Fundamentals of Organic Reactions

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

     Get Reactive Intermediates