Advanced Organic Chemistry Concepts

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A comprehensive set of 50 vocabulary flashcards covering advanced concepts in organic chemistry.

Last updated 3:58 PM on 3/28/26
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46 Terms

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Steric Number

The total number of atoms bonded to a central atom, plus the number of lone pairs on that atom.

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Electronegativity

The tendency of an atom to attract electrons towards itself.

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Homolytic Cleavage

A bond breaking process in which each fragment receives one of the shared electrons.

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Heterolytic Cleavage

A bond breaking process that produces charged species, where one atom receives both electrons.

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Electronic Displacement Effect

The effect observed in a molecule due to the movement of electrons.

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Inductive Effect

A permanent effect which is the shifting of electron density along a chain of atoms in a molecule.

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Resonance

The phenomenon where the electron density is delocalized over two or more adjacent atoms.

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Aromatic Compounds

Compounds that contain a cyclic structure with a conjugated pi electron system.

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Non-Aromatic Compounds

Compounds that do not satisfy the criteria for aromaticity and lack a stable ring structure.

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Anti-Aromatic Compounds

Compounds that have a cyclic structure and a conjugated pi system but are destabilized due to their electron configuration.

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Molecular Orbital Theory

A theory that explains the behavior of electrons in molecules by considering molecular orbitals formed from atomic orbitals.

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Sigma Bond

A covalent bond formed by direct overlap of atomic orbitals.

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Pi Bond

A covalent bond formed by the sideways overlap of p orbitals.

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Delocalization

The spreading of electron density across multiple atoms or orbitals.

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Sp3 Hybridization

A type of hybridization involving one s and three p orbitals, resulting in four equivalent sp3 hybrid orbitals.

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Sp2 Hybridization

A type of hybridization involving one s and two p orbitals, resulting in three sp2 hybrid orbitals.

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Carbene

A reactive species containing a carbon atom with only two bonds and two non-bonding electrons.

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Radical

A species that contains unpaired electrons, making it highly reactive.

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Electrophile

A species that accepts an electron pair from a nucleophile in a chemical reaction.

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Nucleophile

A species that donates an electron pair to an electrophile in a chemical reaction.

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Hydrogenation

The process of adding hydrogen to an unsaturated compound.

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Electrostatic Stability

The stability of a molecule due to the distribution of electric charge among its atoms.

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Hydration Energy

The energy released when ions become hydrated in a solution.

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Conjugate Acid

The species formed when an acid donates a proton (H+).

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Bronsted-Lowry Acid

A substance that can donate a proton in a chemical reaction.

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Bronsted-Lowry Base

A substance that can accept a proton in a chemical reaction.

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Resonance Stabilization

Stabilization of a molecule due to resonance structures or delocalization of electrons.

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Nucleophilic Substitution Reaction

A type of reaction in which a nucleophile replaces a leaving group in a molecule.

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Elimination Reaction

A reaction in which elements of the starting material are removed, forming a double bond.

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Addition Reaction

A reaction where atoms or groups are added to a molecule, usually resulting in saturation.

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Stereoisomerism

Isomerism where compounds have the same molecular formula but differ in the spatial arrangement of atoms.

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Chirality

A property of a molecule that makes it nonsuperimposable on its mirror image.

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Enantiomers

Pairs of chiral molecules that are mirror images of each other.

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Diastereomers

Stereoisomers that are not mirror images of each other.

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Alkane

A saturated hydrocarbon with single bonds only.

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Alkene

An unsaturated hydrocarbon with at least one double bond.

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Alkyne

An unsaturated hydrocarbon that contains at least one triple bond.

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Functional Group

A specific group of atoms within a molecule responsible for characteristic chemical reactions.

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Spectroscopy

An analytical technique used to measure the interaction of light with matter.

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Chromatography

A method for separating mixtures and analyzing compounds.

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IUPAC Nomenclature

The systematic naming of organic chemical compounds based on established rules.

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Hybridization

The mixing of atomic orbitals to form new hybrid orbitals for bonding.

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Rate Law

An equation that relates the rate of a reaction to the concentration of its reactants.

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Catalyst

A substance that increases the rate of a chemical reaction without being consumed.

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Equilibrium Constant (K)

A number that expresses the ratio of the concentrations of products to reactants at equilibrium.

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Activation Energy (Ea)

The minimum energy required for a chemical reaction to occur.

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