2.2.3
Factors Affecting Covalent Bond Strength
After reading these notes, test your knowledge with free interactive questions on Seneca — used by over 10 million students.
Factors Affecting Covalent Bond Strength
The two main factors that affect the strength of a covalent bond are the bond length and bond order.

Bond strength
- A covalent bond is formed when atoms share electron density.
- The binding arises due to the electrostatic attraction between the nuclei of bonding atoms and the electron density in the bond.
- The bond strength is how strongly the atoms in a bond are held together.
- The strength is measured as the amount of energy required to break a mole of bonds in kJ mol-1. This quantity is known as the bond enthalpy.

Bond length
- Bond length is defined as the average distance between the two nuclei of atoms bonded in a molecule.
- The shorter the bond length the stronger the bond and the more energy required to break it (higher bond enthalpy).
- Shorter bonds are between atoms with smaller atomic radii.

Bond length examples
- The relationship between bond length and bond strength is shown by considering the hydrogen halides in the table above.

Bond order
- Bond order is determined by the number of electron pairs in the bonding orbitals between the two atoms in the bond.
- Higher bond orders result in shorter and stronger bonds.
- An example of this is shown in the table above which compares how the increasing bond order of carbon-carbon bonds affects the bond length and bond energy.
Covalent Bond Polarity
Covalent bonds can be polar or apolar, depending on the difference in electronegativity of the bonded elements.

Apolar covalent bonds
- On average, in perfect covalent bonding, the electron density is located halfway between the two nuclei, and the covalent bond is considered to be apolar.
- Apolar covalent bonds are formed between atoms with the same or very similar electronegativities.

Apolar covalent bond example
- The diagram above shows an example of an apolar covalent bond between two chlorine atoms to make a chlorine molecule.

Polar covalent bonds
- Ionic bonds are created when electron density is considered to be completely transferred from one atom to another. The electrostatic attraction between cations and anions holds the ionic lattice together.
- In between the extremes of apolar covalent and ionic bonding, there are polar covalent bonds.

Polar covalent bonds
- When the electronegativity difference between two non-metals in a covalent bond is significant, the electron density in the bond is attracted more strongly to the more electronegative element.
- A dipole is created due to the uneven distribution of electron density, resulting in a polar covalent bond.
- The dipole in a molecule is represented by placing partial charges on the atoms.
- The more electronegative element in the covalent bond has a partial negative charge (δ-) and the less electronegative element has a partial positive charge (δ+).

Polar covalent bond example
- An example of a polar covalent molecule is HCl.
- Chlorine has a greater electronegativity than hydrogen therefore the electron density in the bond is attracted more strongly to chlorine.
- This creates a dipole with chlorine having a partial negative charge (δ-) and hydrogen a partial positive charge (δ+).
1Structure - Models of the Particulate of Matter
1.1Introduction to the Particulate Model of Matter
1.2The Nuclear Atom
1.3Electron Configuration
1.4Counting Particles by Mass: The Mole
1.6Elements, Compounds & Mixtures
1.7States of Matter & Changes of State
1.8Reacting Masses &. Volumes
1.9Solutions
2Structure - Models of Bonding & Structure
2.1The Ionic Model
2.2The Covalent Model
2.3Covalent Structures
2.4The Metallic Model
2.5From Models to Materials
2.6Valence Electrons & Ionic Compounds
2.7Molecular Shape
3Structure - Classification of Matter
3.1The Periodic Table: Classification of Elements
3.2Periodic Trends
3.3Group 1 Alkali Metals
3.4Halogens
3.5Noble gases, group 18
3.6Functional Groups: Classification of Organic
3.7Functional Group Chemistry
3.8Alkanes
3.9Alcohols
4Reactivity - What Drives Chemical Reaction?
4.1Endothermic & Exothermic Reactions
4.2Enthalpy of Reaction, Formation, & Hess' Law
5Reactivity - How Much, How Fast & How Far?
5.1Kinetics
5.2Rates of Reaction
5.3Stoichometry
5.4Le Châtelier’s Principle
5.5Introduction to Equilibrium
5.6Equilibrium Constant
5.7Reaction Quotient & Equilibrium Constant
6Reactivity - The Mechanisms of Chemical Change
6.1Proton Transfer Reactions
6.2The pH Scale
6.3Strong & Weak Acids and Bases
6.4Acid Deposition
6.5Types of Organic Reactions
6.6Oxidation & Reduction
6.7Electrochemical Cells
6.9Acid-Base Titrations
6.9.1Titration Calculation Weak Acid & Strong Base6.9.2Titration Experimental Detail6.9.3Extended Response - Titration6.9.4Titration Calculations6.9.5Titration Curves6.9.6Titration Calculation Strong Acid & Weak Base6.9.7IB Multiple Choice - Titrations6.9.8Polyprotic Acids6.9.9Titration Calculations Strong Acid & Strong Base6.9.10Titrations Curves 2
7Measurement, Data Processing & Analysis
7.1Uncertainties & Errors in Measurements & Results
7.2Graphical Techniques
7.3Spectroscopic Identification of Organic Compounds
7.4Infrared Spectroscpy
Jump to other topics
1Structure - Models of the Particulate of Matter
1.1Introduction to the Particulate Model of Matter
1.2The Nuclear Atom
1.3Electron Configuration
1.4Counting Particles by Mass: The Mole
1.6Elements, Compounds & Mixtures
1.7States of Matter & Changes of State
1.8Reacting Masses &. Volumes
1.9Solutions
2Structure - Models of Bonding & Structure
2.1The Ionic Model
2.2The Covalent Model
2.3Covalent Structures
2.4The Metallic Model
2.5From Models to Materials
2.6Valence Electrons & Ionic Compounds
2.7Molecular Shape
3Structure - Classification of Matter
3.1The Periodic Table: Classification of Elements
3.2Periodic Trends
3.3Group 1 Alkali Metals
3.4Halogens
3.5Noble gases, group 18
3.6Functional Groups: Classification of Organic
3.7Functional Group Chemistry
3.8Alkanes
3.9Alcohols
4Reactivity - What Drives Chemical Reaction?
4.1Endothermic & Exothermic Reactions
4.2Enthalpy of Reaction, Formation, & Hess' Law
5Reactivity - How Much, How Fast & How Far?
5.1Kinetics
5.2Rates of Reaction
5.3Stoichometry
5.4Le Châtelier’s Principle
5.5Introduction to Equilibrium
5.6Equilibrium Constant
5.7Reaction Quotient & Equilibrium Constant
6Reactivity - The Mechanisms of Chemical Change
6.1Proton Transfer Reactions
6.2The pH Scale
6.3Strong & Weak Acids and Bases
6.4Acid Deposition
6.5Types of Organic Reactions
6.6Oxidation & Reduction
6.7Electrochemical Cells
6.9Acid-Base Titrations
6.9.1Titration Calculation Weak Acid & Strong Base6.9.2Titration Experimental Detail6.9.3Extended Response - Titration6.9.4Titration Calculations6.9.5Titration Curves6.9.6Titration Calculation Strong Acid & Weak Base6.9.7IB Multiple Choice - Titrations6.9.8Polyprotic Acids6.9.9Titration Calculations Strong Acid & Strong Base6.9.10Titrations Curves 2
7Measurement, Data Processing & Analysis
7.1Uncertainties & Errors in Measurements & Results
7.2Graphical Techniques
7.3Spectroscopic Identification of Organic Compounds
7.4Infrared Spectroscpy
Practice questions on Factors Affecting Covalent Bond Strength
Can you answer these? Test yourself with free interactive practice on Seneca — used by over 10 million students.
- 1What is the correct unit for bond enthalpy?Multiple choice
- 2Which of these statements is NOT correct?Multiple choice
- 3
Unlock your full potential with Seneca Premium
Unlimited access to 10,000+ open-ended exam questions
Mini-mock exams based on your study history
Unlock 800+ premium courses & e-books