User:Benjah-bmm27/degree/1/PJW

=Structure and reactivity, PJW=

Levels of structure

 * The structure and geometry of molecules, comprising:
 * Chemical formulas
 * Empirical formulas
 * Molecular formulas
 * Connectivity
 * Structural formulas
 * Lewis structures
 * Skeletal formulas
 * Configuration
 * Absolute configuration (basically which enantiomer)
 * use Cahn–Ingold–Prelog priority rules to determine the correct stereochemical label for a stereocentre based on its absolute configuration
 * for asymmetric carbon, use R-S notation
 * for cis-trans isomerism, use E-Z notation
 * Conformation (3D shape that can change without breaking and making bonds, by rotation about bonds)

Connectivity is the domain of regiochemistry, whereas configuration and conformation come under stereochemistry.

Table of types of structure and isomerism

 * Law of definite proportions
 * Asymmetry
 * Chirality (mathematics)
 * Chirality (physics) including chiral symmetry
 * Chirality (chemistry)
 * Chiral ligand
 * Asymmetric synthesis, asymmetric induction
 * Axial chirality
 * Inherent chirality
 * Supramolecular chirality

IUPAC Gold Book definitions

 * Compendium of Chemical Terminology, commonly known as the IUPAC Gold Book
 * connectivity: "In a chemical context, the information content of a line formula, but omitting any indication of bond multiplicity."
 * constitution: "The description of the identity and connectivity (and corresponding bond multiplicities) of the atoms in a molecular entity (omitting any distinction arising from their spatial arrangement)."
 * superposability: "The ability to bring two particular stereochemical formulae (or models) into coincidence (or to be exactly superposable in space, and for the corresponding molecular entities or objects to become exact replicas of each other) by no more than translation and rigid rotation."
 * projection formula
 * absolute configuration
 * relative configuration
 * configuration (stereochemical): "...the arrangements of atoms of a molecular entity in space that distinguishes stereoisomers, the isomerism between which is not due to conformation differences."
 * conformer
 * rotamer
 * polytopal rearrangement

Relationship between structure, bonding, and electrons

 * Resonance between Lewis structures and the associated delocalisation of electrons
 * Orbital hybridisation
 * part of valence bond theory, together with pair bonding and resonance
 * Hybridization Theory, a YouTube preview of an educational DVD
 * Molecular orbital theory
 * less useful than valence bond theory for day-to-day back-of-the-envelope organic chemistry but an exceptionally powerful tool for more a detailed, precise, accurate and fundamental understanding of chemical bonding
 * for more detail, see:
 * Level 1 quantum mechanics
 * Level 2 quantum mechanics
 * Level 2 molecular orbital theory
 * Level 2 Hückel theory
 * Level 3 orbitals in organic chemistry
 * Level 3 molecular electronic structure
 * Level 3 molecular spectroscopy and structure

Orbitals and axial chirality

 * Allenes, R2C=C=CR2 &mdash; can exhibit axial chirality due to orthogonal pi bonds
 * Ketenes, R2C=C=O, also have orthogonal pi bonds but no substituents on oxygen, so ketenes do not exhibit axial chirality

Reactivity

 * Chemical reactions involve the movement of electrons between chemicals (e.g. redox), usually resulting in the making and breaking of chemical bonds
 * Oxidation levels in organic compounds
 * The chemicals taking part in a reaction can best be categorised as acids, bases, nucleophiles, or electrophiles. There are several acid-base reaction theories but the one we're talking about is the Brønsted–Lowry acid-base theory.

Acids vs. bases

 * Acids are proton donors. They do one thing: protonate.
 * Bases are proton acceptors. They also do one thing: deprotonate.

Electrophiles vs. nucleophiles

 * Electrophiles are electron acceptors (≈ Lewis acids), as are oxidizing agents
 * Nucleophiles are electron donors (≈ Lewis bases), as are reducing agents

Hard and soft

 * Electrophiles and nucleophiles can each be further classified as hard or soft, or more realistically, where they lie along the hard-soft spectrum
 * For details, see later courses on dicarbonyl compounds, retrosynthetic analysis, orbitals in organic chemistry
 * Hard electrophiles react best with hard nucleophiles, as they have:
 * small atomic or ionic radii
 * high oxidation states
 * low polarizabilities
 * high electronegativities
 * low-lying HOMOs (nucleophiles) or energy high-lying LUMOs (electrophiles)
 * if the reacting electrophile and nucleophile are very hard, redox can happen (formally, complete transfer of electrons from nucleophile to electrophile instead of sharing)
 * Soft electrophiles react best with soft nucleophiles, as they have:
 * large atomic or ionic radii
 * low (or zero) oxidation states
 * high polarizabilities
 * low electronegativities
 * high-lying HOMOs (nucleophiles) and low-lying LUMOs (electrophiles)
 * HSAB theory is also used in inorganic chemistry: Level 2 transition metal chemistry (hard and soft metals and ligands)

Substitution reactions

 * Nucleophilic substitution:
 * SN1 goes with racemization
 * SN2 goes with inversion
 * SN2 animation
 * The true mechanism may be more complicated in some cases
 * Nucleophilic acyl substitution: esterification, transesterification, ester hydrolysis