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Summary Sheet
Lewis Structures and Formal Charge
- Position most electropositive atom in the middle, with more electronegative atoms around it
- Add valence electrons (be aware of overall molecule charge) and form bonds between the central and terminal atoms (1 bond = 2 electrons)
- Complete the octets of the terminal atoms by moving electrons out from the central atom
- Calculate formal charges and add double bonds if necessary
- Check to make sure all atoms have complete octets, and that if they don't it is allowed*
Carbon and Nitrogen can ONLY form 4 bonds!!!
Formal charge is calculated using the following equation:
FC(atom) = # valence e- - (lone pair e- + number of bonds)
Key Terms
- Valence Bond Theory: Defines the orbitals involved in bonding for each atom in a compound.
- Hybridization: The combination of atomic orbitals (usually s and p orbitals) to form bonding orbitals
- Molecular Orbital (MO) Theory: How the (usually hybridized) atomic orbitals combine to form bonds. Each bond involves the formation of a bonding (either a σ-bond or π-bond) and a related antibonding (σ*-bond or π*-bond) orbital by overlapping orbitals.
- Resonance: The state attributed to certain molecules of having a structure that cannot adequately be represented by a single structural formula but is a composite of two or more structures of higher energy.
- Valence-Shell Electron-Pair Repulsion (VSEPR): The geometry and shape of a molecule is dictated by the atom's hybridization (number of σ-bonds and π-bonds). It is important to consider lone pairs, they also occupy space!
- Electronegativity: Tendency of an atom to bring electrons close, in a bond.
- Polarity: For a molecule to be overall polar (posses a net dipole) it needs: 1. A Polar Covalent Bond 2. Appropriate Geometry.
- Intermolecular Forces: Attractions between compounds holding them together that influence their relative boiling and melting points. More (stronger) intermolecular forces = higher boiling/melting points.
