chemical Bonding Chapter 4
Overview of Lewis Structures and Electron Configuration
Introduction to Lewis Structures
The session is focused on practicing the drawing of Lewis structures.
Lewis Structure Rules
Reminder to review Lewis structure rules previously discussed.
Practice Assignments
Students are encouraged to try drawing three Lewis structures during the class.
Peer collaboration is allowed.
Example Lewis Structures
Phosphorus Trihydride (PH₃)
Description: Phosphorus trihydride, where phosphorus acts as the central atom.
Key Points:
Hydrogen:
Never a central atom; always terminal.
Requires only two electrons.
Phosphorus Valence Electrons:
5 from phosphorus and 3×1 from hydrogen gives a total of 8 electrons.
Electrons Count:
Establish a single bond (2 electrons):
Total after bonding: 2 + 2 + 2 = 6 (for the three bonds made).
Remaining electrons: 2 electrons placed as a lone pair on phosphorus, achieving an octet.
Perchlorate Anion (ClO₄⁻)
Identification: Chlorine as the central atom due to lower electronegativity compared to oxygen.
Calculating Electrons:
Chlorine contributes 7 electrons, and each oxygen contributes 6 (4×6 = 24 total).
Count of electrons around oxygen: Initial 2 electrons, needs a total of 6.
Remaining electrons must account for the chloride to maintain a complete structure.
Charge Representation:
Charge brackets with designation of negative charge in upper right. Only done for ions.
Carbonate Anion (CO₃²⁻)
Carbon is the default central atom.
Electron Contribution:
Carbon provides 4 valence electrons, and the 3 oxygens contribute 6 each (3×6 = 18).
Total: 4 + 18 + 2 (from the negative charge) = 24 electrons available.
Bonding Analysis: Each oxygen requires 2 additional electrons to reach an octet after creating bonds.
Double Bonds: Create double bonds to fulfill the octet requirement due to insufficient electrons.
Resonance Structures: Multiple diagrams acceptable for the same molecule, denoted by double-headed arrows, indicating flexibility in electron placement.
Key Concepts of Structures
Resonance
Definition: Structures where electrons are not fixed but rather distributed among equivalent configurations.
Stability: Delocalized electrons lead to stability in bonding arrangements.
Formal Charge
Definition: A method to ensure structures with minimized charge distribution are preferred.
Calculation:
Formula:
Formal Charge = Valence Electrons - (Bonds + Lone Pairs)
Importance in validating Lewis structures through minimized charge across atoms.
Exceptions to Lewis Structures
Hypervalency
Description: Atoms from row 3 and beyond can hold more than 8 electrons in their valence shell. Examples: Phosphorus pentafluoride (PF₅).
Hypovalency
Description: Certain elements like boron are stable with fewer than 8 electrons. Boron trifluoride (BF₃) is a common example.
Odd-Electron Species
Examples: Free radicals such as nitric oxide (NO) and nitrogen dioxide (NO₂).
Significance: Reactive and can lead to environmental concerns, such as smog formation.
Molecular and Electron Pair Geometry
Definitions
Electron Pair Geometry: Arrangement based solely on electron regions around a central atom.
Molecular Geometry: Defines the spatial positioning based on both electron regions and types of bonds (single, double, or triple).
Types of Electron/ Molecular Geometries:
Linear
Trigonal Planar
Tetrahedral
Trigonal Bipyramidal
Octahedral
Effects of Lone Pairs on Geometry
Lone pairs minimize bond angles, leading to molecular geometries that differ from electron pair geometries.
Example:
Tetrahedral (109.5° bond angle) with one lone pair transforms to a bent (less than 109.5°) shape.
Conclusion of Session
Students are encouraged to apply these concepts in further practice with Lewis structures, focusing particularly on identifying molecular shapes, predicting stability, and understanding resonance.
Next session will continue exploring molecular geometries and bonding arrangements.