• Alcoholsv
  • Phenols
  • Properties of Alcohols
  • Reactions of Alcohols
  • Synthesis of Alcohols
• Aldehydes and Ketonesv
  • Properties of Aldehydes & Ketones
  • Reactions of Aldehydes & Ketones
  • Synthesis of Aldehydes & Ketones
• Amidesv
  • Properties of Amides
  • Reactions of Amides
  • Synthesis of Amides
• Aminesv
  • Properties of Amines
  • Reactions of Amines
  • Synthesis of Amines
• Carboxylic Acidsv
  • Properties of Carboxylic Acids
  • Reactions of Carboxylic Acids
  • Synthesis of Carboxylic Acids
• Case Studiesv
  • Case Study: Fossil Fuels
  • What is Organic?
• Chiralityv
  • Absolute Configuration: R-S Sequence Rules
  • Chirality and Stereoisomers
  • Diastereomers
  • Fischer Projections
  • Fundamentals of Chirality
  • Meso Compounds
  • Optical Activity
• Conjugationv
  • Conjugated Dienes
  • Electrophilic Attack on Conjugated Dienes-Kinetic and Thermodynamic Control
  • Overlap of Adjacent p Orbitals-Electron Delocalization
  • Polymerization of Conjugated Dienes
  • The Diels-Alder Cycloaddition
• Estersv
  • Properties of Esters
  • Reactions of Esters
  • Synthsis of Esters
• Ethersv
  • Properties of Ethers
  • Reactions of Ethers
  • Synthesis of Ethers
• Fundamentalsv
  • Coulomb Forces
  • Electrophiles & Nucleophiles
  • Hybrid Orbitals
  • Index of Hydrogen Deficiency (IHD)
  • Ionic and Covalent Bonds
  • Lewis Structures
  • Molecular Classes
  • Omitting numbers
  • Resonance Forms
  • Rotation in Substituted Ethanes
  • Structure of Organic Molecules
  • The phenyl group
• Hydrocarbonsv
  • Alkanes
  • Alkenes
  • Alkynes
  • Aromatics
• Organic Chemistry With a Biological Emphasisv
  • Appendix I: Index of enzymatic reactions by pathway
  • Appendix: Review of laboratory synthesis reactions
  • Chapter 1: Introduction to organic structure and bonding I
  • Chapter 10: Phosphoryl transfer reactions
  • Chapter 11: Nucleophilic carbonyl addition reactions
  • Chapter 12: Acyl substitution reactions
  • Chapter 13: Reactions with stabilized carbanion intermediates I
  • Chapter 14: Reactions with stabilized carbanion intermediates II
  • Chapter 15: Electrophilic reactions
  • Chapter 16: Oxidation and reduction reactions
  • Chapter 17: Radical reactions
  • Chapter 2: Introduction to Organic Structure and Bonding II
  • Chapter 3: Conformations and Stereochemistry
  • Chapter 4: Structure Determination I: UV-Vis and Infrared Spectroscopy, Mass Spectrometry
  • Chapter 5: Structure Determination II: Nuclear Magnetic Resonance
  • Chapter 6: Introduction to organic reactivity and catalysis
  • Chapter 7: Organic compounds as acids and bases
  • Chapter 8: Nucleophilic substitution reactions, part I
  • Chapter 9: Nucleophilic substitution reactions, part II
  • Full Table of Contents
  • Introduction
  • Reference Tables
  • Solution Manual
• Polymersv
  • Addition Polymers
  • Condensation Polymers
  • Polyethylene
  • Polymer Fundamentals
  • Rubber Polymers
  • Silicone Polymers
• Reactionsv
  • Addition Reactions
  • E1 Reaction
  • E2 Reaction
  • Elimination Reactions
  • Kinetics of Nucleophilic Substitution Reactions
  • Oxymercuration-Demercuration: A Special Electrophilic Addition
  • Pushing Arrows
  • Rearrangement Reactions
  • SN1
  • SN2
  • Substitution Reactions
  • The Generalized Electrophilic Addition
• Videos
• Virtual Textbook of OChemv
  • Alcohols
  • Aldehydes & Ketones
  • Alkanes
  • Alkenes
  • Alkyl Halides
  • Alkynes
  • Aromaticity
  • Benzene
  • Biochemicals
  • Carboxyl Derivatives
  • Chemical Reactivity
  • Ethers
  • Intermolecular Forces
  • Nomenclature
  • Phosphines
  • Spectroscopy
  • Stereoisomers
  • Structure & Bonding
  • Thiols and Sulfides

Esters are known for their distinctive odors and are commonly used for food aroma and fragrances. The general formula of an ester is RCOOR'.

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