When electromagnetic radiation in the ultraviolet (UV) or visible region of the spectrum is absorbed by a molecule, π or non-bonding (n) electrons are promoted into antibonding orbitals. Because the main electron transitions are π→π* transitions, the absorption of energy in the UV or visible range (200–700 nm) usually indicates the existence of π bond(s) and an unsaturated compound. Conversely, molecules that don't absorb in the UV or visible region don't contain an unsaturated system. The strength of the absorption, measured by its extinction coefficient, ε, is determined by the amount of conjugation in the system. The position of an absorption is determined to a large extent by the relative mobility of the π electrons.
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- Preparations: Alkyl Halides
- Preparations: Phenols
- Preparations: Aryl Halides
- Preparations: Ethers
- Preparations: Alcohols
- Preparations: Aldehydes
- Preparations: Ketones
- Preparations: Carboxylic Acids
- Preparations: Halo Acids, α‐Hydroxy Acids, and α, β‐Unsaturated Acids
- Preparations: Amines
- Reactions: Aromatic Compounds
- Reactions: Alkyl Halides
- Reactions: Phenols
- Reactions: Aryl Halides
- Reactions: Ethers
- Reactions: Alcohols
- Reactions: Aldehydes and Ketones
- Reactions: Carboxylic Acids
- Reactions: Esters
- Reactions: Acyl Halides
- Reactions: Anhydrides
- Reactions: Amines
- Introduction to Aromatic Compounds
- Benzene
- Hückel's Rule
- Other Aromatic Compounds
- Heterocyclic Aromatic Compounds
- Electrophilic Aromatic Substitution Reactions
- The Birch Reduction of Benzene
- Friedel‐Crafts Alkylation Reaction
- Friedel‐Crafts Acylation Reaction
- Directing Group Influence
- Theory of Substitution Effects
- Introduction to Alkyl Halides
- Nucleus and Nucleophiles
- Nucleophilic Substitution Reactions
- Leaving Group
- Nucleophilic Substitution Reactions: Mechanisms
- SN1 versus SN2 Reactions
- Elimination Reactions
- Mechanism of Elimination Reactions
- Grignard Reaction
- Preparation of Alkyl Halides
- Phenols
- Synthesis of Phenols
- Reactions of Phenolic Hydrogen
- Reactions of Phenolic Benzene Rings
- Aryl Halides
- Synthesis of Aryl Halides
- Reactions of Aryl Halides
- Introduction to Carboxylic Acids
- Preparation of Carboxylic Acids
- Reactions of Carboxylic Acids
- Reduction of Carboxylic Acids
- Introduction: Spectroscopy and Structure
- Mass Spectra
- Nuclear Magnetic Resonance (NMR) Spectra
- Ultraviolet and Visible Spectra
- Infrared Spectra
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Ultraviolet and Visible Spectra
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Summary of Preparations
Spectroscopy and Structure
