Bonding: General Concepts
Bonding: General Concepts
Source: Chapter 3 Zumdahl, CHEMISTRY: An Atoms First Approach, Third Edition. © 2021 Cengage.
Table of Contents
Section 3.1: Types of chemical bonds
Section 3.2: Electronegativity
Section 3.3: Ions: Electron configurations and sizes
Section 3.4: Partial ionic character of covalent bonds
Section 3.5: The covalent chemical bond: A model
Section 3.6: The localized electron bonding model
Section 3.7: Lewis structures
Section 3.8: Exceptions to the octet rule
Section 3.9: Resonance
Section 3.10: Naming simple compounds
Questions to Consider
What is meant by the term “chemical bond”?
Why do atoms bond with each other to form compounds?
How do atoms bond with each other to form compounds?
Section 3.1: Types of Chemical Bonds
Chemical Bond Definition: The force that holds atoms together is called a chemical bond.
Covalent Bond:
Formed when atoms share electrons.
A collection of atoms makes a molecule.
Molecular Representations:
Chemical Formula: Example CO2
Structural Formula: Example H—O—H
Space-filling Model: Indicates both relative sizes of atoms and their orientation in the molecule.
Ball and Stick Model: A three-dimensional model using spheres (atoms) and rods (bonds).
Attributes of Molecules
Physical Properties include:
Melting Point
Hardness
Electrical and Thermal Conductivity
Solubility
Electric Charge
Bond Energy: The amount of energy needed to break a bond.
Types of Chemical Bonding
Ionic Bonding:
Occurs between an atom that easily loses electrons (typically metals) and an atom that has a high affinity for electrons (typically non-metals).
Ionic compounds are typically formed when metals react with non-metals.
Coulomb’s Law
Used to calculate the energy of interaction between ions:
Formula:
E = k rac{Q1 Q2}{r}
where:E: Energy, units in joules
r: Distance between ions in nanometers
Q1 and Q2: Numerical charge values of the ions.
Stability of Atoms in Bonding
Example:
In the H2 molecule, electrons reside in the space between two nuclei leading to increased stability compared to single H atoms.
Increased attractive forces result in a decrease in the potential energy of electrons.
Polar Covalent Bond
Definition: Unequal sharing of electrons between atoms in a molecule.
Results in charge separation within the bond, creating partial positive (δ+) and partial negative (δ−) charges.
Section 3.2: Electronegativity
Definition: The ability of an atom in a molecule to attract shared electrons to itself.
Pauling Method:
For a molecule HX, relative electronegativities of H and X are assessed by comparing bond energies:
Actual Bond Energy vs. Expected Bond Energy.
Determining Values of Electronegativity
Charge distribution based on electronegativity differences can be understood through variations in bond energy:
Formula:
\Delta E = ext{Actual Bond Energy - Expected Bond Energy}
If Δ = 0, H and X have identical electronegativities.
If the electronegativity of X exceeds that of H, shared electrons are closer to atom X, influencing charge distribution.
Table 3.1: Relationship Between Electronegativity and Bond Type
List of Bonds Ordered by Polarity based on their electronegativity differences (values provided in parentheses):
H—H (2.1), S—H (2.1), Cl—H (3.0), O—H (3.5), F—H (4.0)
Section 3.3: Ions - Electron Configurations and Sizes
Electron Configuration in Compounds:
In a reaction between two nonmetals, electron sharing enables both to achieve a complete valence electron configuration, imitating noble gas states.
In reactions involving nonmetals and representative-group metals, binary ionic compounds are formed; ions achieve noble gas configurations.
Concept Check: Isoelectronic Series
Task: Choose ions from alkali metals, alkaline earth metals, noble gases, and halogens that form an isoelectronic series.
Concepts Involved:
Electron configurations, number of electrons and protons, and physical properties including ionic radius and ionization energy.
Predicting Formulas of Ionic Compounds
Definition of Ionic Compounds:
Chemists define these as compounds in solid states where the attraction between positive and negative ions is maximized due to close proximity.
Example of valence electron configurations:
Calcium: ext{Ca} [ ext{Ar}]4s^2
Oxygen: ext{O} [ ext{He}]2s^22p^4
Since oxygen has a higher electronegativity than calcium, the prediction of compound formulas can be established for consistency with stable noble gas configurations.
Sizes of Ions
Factors influencing ionic size:
Size of the parent atom.
Position in the periodic table: Isoelectronic ions contain the same number of electrons.
Section 3.4: Partial Ionic Character of Covalent Bonds
Percent Ionic Character Formula:
No bond is 100% ionic; thus the ionic character is calculated through comparative studies.
Example of calculating ionic character from electronegativity differences across various bonds and determining the effect of bond type on ionic character.
Ionic Compounds
Identification Problems:
No bond considered fully ionic; many substances comprise polyatomic ions.
Operational definition: Any compound conducting electricity when melted is classified as ionic.
Section 3.5: The Covalent Chemical Bond - A Model
Models Overview:
Used to explain microscopic behaviors based on macro observations and properties.
Provide frameworks that help understand chemical behaviors, emphasizing that models simplify reality.
Section 3.6: The Localized Electron Bonding Model
Localized Electron (LE) Model:
Molecules consist of atoms bound through shared electron pairs from atomic orbitals.
Lone pairs: Non-bonding electron pairs on atoms.
Bonding pairs: Found in space between atoms.
Lewis Structures
Definition: Illustrates valence electron arrangement in molecules, named after G. N. Lewis.
Principles of Writing Lewis Structures:
Sum of valence electrons from all atoms.
Use a pair of electrons to bond atoms.
Arrange remaining electrons to fulfill the duet rule for hydrogen and octet rule for row 2 elements.
Exceptions to the Octet Rule
Boron Compounds: Tends to have fewer than eight electrons around it (boron fluoride example).
Adding double bonds can achieve an octet.
Exceeding the Octet Rule: Seen in elements from Period 3 or beyond, e.g., sulfur hexafluoride.
Resonance
Definition: More than one valid Lewis structure for some molecules.
Example: Nitrate ion (NO3-); true molecular structure is a superposition of all valid structures.
Formal Charge
Definition: Used for estimating the charge on atoms in Lewis structures:
Formula:
ext{Formal charge} = ( ext{valence electrons}) - ( ext{assigned electrons})
Assumptions: Lone pairs belong entirely to an atom, while shared electrons are divided equally.
Naming Simple Compounds
Binary Ionic Compounds (Type I):
Compounds consist of a cation followed by an anion.
Rules: Cation named first, anion named second as -ide root.
Example Table:
Cation: H+, Li+, Na+, etc.
Anion: H− (hydride), F− (fluoride), etc.
Binary Ionic Compounds (Type II)
Metals forming more than one type of positive ion are named using Roman numerals to signify charge.
Naming rules adjust based on higher (-ic) or lower (-ous) charge nomenclature.
Oxyanions
Specific naming conventions depending on oxygen presence:
-ate for higher, -ite for lower, -hypo and -per for additional variations in oxygen content.
Acids
Naming rules based on anion suffixes:
-ide becomes hydra- and -ic, while -ate becomes -ic and -ite becomes -ous.
Example acids:
HCl (hydrochloric acid), H2SO4 (sulfuric acid).