BackGeneral Chemistry Study Notes: Atomic Structure, Bonding, and Molecular Properties
Study Guide - Smart Notes
Tailored notes based on your materials, expanded with key definitions, examples, and context.
Atomic Structure
Atoms and Isotopes
The atom is the fundamental unit of matter, consisting of a nucleus (protons and neutrons) surrounded by electrons.
Atomic Number (Z): The number of protons in the nucleus of an atom. Determines the element's identity.
Mass Number (A): The sum of protons and neutrons in the nucleus.
Isotopes: Atoms of the same element (same Z) with different numbers of neutrons (different A).
Example: Hydrogen has three isotopes: Hydrogen (1 proton), Deuterium (1 proton, 1 neutron), Tritium (1 proton, 2 neutrons).
Ions: Atoms that have gained or lost electrons. Positively charged ions are cations; negatively charged ions are anions.
Example: Proton (H+), Hydride (H-).
Electron Configuration Principles
Electrons occupy regions of space called orbitals. The arrangement of electrons in an atom follows three main principles:
Aufbau Principle: Electrons fill the lowest energy orbitals first.
Pauli Exclusion Principle: No two electrons in an atom can have the same set of quantum numbers; each orbital holds a maximum of two electrons with opposite spins.
Hund's Rule: Electrons fill degenerate orbitals singly before pairing.
Example: Electron configuration diagrams show how electrons fill orbitals according to these rules.
Electron Configuration
Ground State Electron Configuration
The distribution of electrons among the orbitals of an atom in its lowest energy state.
Aufbau Principle: Start from 1s, fill lower energy orbitals before higher energy ones.
Condensed Electron Configuration: Use the previous noble gas to abbreviate the configuration.
Example: Phosphorus (Z = 15): Ground state: Condensed:
Block | Elements |
|---|---|
s-block | Groups 1A, 2A |
p-block | Groups 3A-8A |
d-block | Transition metals |
f-block | Lanthanides & Actinides |
Electronegativity
Definition and Periodic Trend
Electronegativity (EN): A measure of an atom's ability to attract electrons in a chemical bond.
Periodic Trend: Electronegativity increases from left to right across a period and increases going up a group.
Example: The most electronegative Group 7A element is Cl (Chlorine).
Octet Rule
Valence Electrons and Shared Electrons
The tendency of main group elements to achieve eight electrons in their valence shell through chemical bonding.
Valence Electrons: Electrons in the outermost shell, involved in bonding.
Shared Electrons: Electrons shared between atoms in a chemical bond.
Example: In H3C–O–H, oxygen has 6 valence electrons and 2 shared electrons, totaling 8 octet electrons.
Formal Charge
Calculating Formal Charge
Formal charge helps determine the most stable Lewis structure for a molecule.
Only allowable formal charges: -1, 0, +1
The sum of formal charges equals the overall charge of the molecule/ion.
Formula: Formal Charge = Valence Electrons – (Nonbonding Electrons + 1/2 Bonding Electrons)
Example: Calculate formal charges for N, C, and S in the thiocyanate ion (NCS-).
Lewis Dot Structures
Drawing Lewis Structures
Lewis structures represent the arrangement of valence electrons in molecules.
Count total valence electrons.
Place the least electronegative atom in the center (except H and halogens).
Connect atoms with single bonds.
Complete octets for surrounding atoms.
Place remaining electrons on the central atom.
If octets are not complete, form double/triple bonds as needed.
Check formal charges for stability.
Example: Draw the Lewis structure for COCl2.
Resonance Structures
Definition and Representation
Resonance structures are two or more valid Lewis structures for a molecule or ion that differ only in the placement of electrons.
Movement of electrons occurs in pi bonds or lone pairs.
Double-sided arrows indicate resonance between structures.
The actual structure is a resonance hybrid, a composite of all resonance forms.
Example: Draw all resonance structures for the nitrate ion, NO3-.
Hybridization
Electron Groups and Hybrid Orbitals
Hybridization describes the mixing of atomic orbitals to form new hybrid orbitals suitable for bonding.
Electron Groups: Number of bonds and lone pairs around the central atom.
Electron Groups | Hybridization | Geometry |
|---|---|---|
2 | sp | Linear |
3 | sp2 | Trigonal Planar |
4 | sp3 | Tetrahedral |
Example: HCN has 2 electron groups, so the central atom is sp hybridized.
Molecular Polarity
Polar and Nonpolar Molecules
Molecular polarity arises from the distribution of electron density in a molecule.
Nonpolar Molecule: Hydrocarbons and molecules with perfect symmetry.
Polar Molecule: Molecules with an asymmetric distribution of electrons.
Electron Groups | Lone Pairs | Polarity |
|---|---|---|
2 | 0 | Nonpolar |
3 | 1 | Polar |
4 | 2 | Polar |
Example: Nitrogen trifluoride (NF3) is polar due to lone pairs and asymmetry.
Functional Groups
Definition and Classification
A functional group is a specific group of atoms within a molecule responsible for characteristic chemical reactions.
Hydrocarbons: Alkanes, alkenes, alkynes, aromatic compounds.
With Carbonyls: Aldehyde, ketone, acid chloride, amide, carboxylic acid, ester.
Without Carbonyls: Alkyl halide, amine, alcohol, ether, thiol.
Functional Group | Structure |
|---|---|
Alcohol | R–OH |
Aldehyde | R–CHO |
Ketone | R–CO–R' |
Carboxylic Acid | R–COOH |
Amine | R–NH2 |
Ether | R–O–R' |
Organic Chemistry Overview
Organic Molecules and Hydrocarbons
Organic chemistry studies molecules containing carbon and hydrogen, often with other elements.
Organic Molecule: Contains both carbon and hydrogen.
Hydrocarbon: Contains only carbon and hydrogen.
Example: Identify organic molecules and hydrocarbons from given structures.
Additional info:
Some context and examples were inferred to provide complete academic explanations.
Tables were recreated to summarize block classification, hybridization, molecular polarity, and functional groups.