• Home
  • Organic chemistry
  • Advanced Organic
  • Heterocycles
  • Synthesis
  • Spectroscopy
  • Reactions
  • Bahasa Indonesia
  • Português (Portugal)
  • Русский (Россия)
  • Italiano (Italia)
  • Deutsch (Deutschland)
  • Español (forma internacional)
  • Français (France)
  • English (UK)

Tell me what you need?

Organic Chemistry Book

book

Organic Nomenclature Book

nomenclature box

THE MOST READ

  • Alkanes nomenclature
  • Isomer classification
  • Physical properties of alkanes
  • Geometric or cis-trans isomers
  • Types of hydrocarbons
  • Isomeric alkanes
  • The 20 amino acids that make up proteins
  • Alkene Nomenclature
  • Alkanes
  • Alcohol Nomenclature
  • Alcohols - general characteristics
  • Physical properties of ethers
  • Alcohol oxidation
  • Cycloalkanes nomenclature
  • Molecular chirality and enantiomers
  • Benzene nomenclature
  • Physical properties of Alkynes
  • Anhydride Nomenclature
  • Amino Acids - Isoelectric Point
  • Newman projection
  • Synthesis of Carboxylic Acids
  • Amine Nomenclature
  • Alkene Hydration
  • Nomenclature - Carboxylic Acids
  • Optical activity
  • Fisher projection
  • Alkenes hydrogenation
  • Physical Properties of Alkenes
  • Ozonolysis of Alkenes
  • Enantiomer nomenclature
  • Benzene Nitration
  • Synthesis of Alkenes by Dehydration of Alcohols
  • Physical properties of amines
  • Degree of unsaturation
  • conformational isomers
  • Sulfonation of benzene
  • Acidity and basicity of alcohols
  • Physical Properties of Carboxylic Acids
  • Electrophilic addition reactions
  • Conformational analysis of ethane
  • Synthesis of esters from carboxylic acids - Esterification
  • Alkyne nomenclature
  • Stereochemistry - Stereoisomerism
  • aldol condensation
  • Isomers with a single asymmetric carbon
  • Williamson's synthesis of ethers
  • Haloform (Iodoform) reaction
  • halogenation of benzene
  • Synthesis of ethers by condensation of alcohols
  • Ethers - epoxides nomenclature
  • Symmetry in Chiral Molecules: Meso Forms
  • Markovnikov Rule - Regioselectivity
  • Alkynes
  • Halogenation of Alkynes
  • Halogen addition
  • Synthesis of Alcohols by reduction of carbonyls
  • Alkene polymerization
  • RS Notation on Fischer Projection
  • Alkyne hydrogenation
  • Passage from Newman to Fischer
  • Alkyne Hydration
  • Formation of Alkoxides from Alcohols
  • Sawhorse projection
  • Butane conformational analysis
  • Electrophilic Aromatic Substitution
  • Acidity and Basicity of Carboxylic Acids
  • Synthesis of Alkynes by Alkylation
  • Ring Strain in Cycloalkanes
  • Synthesis of Alcohols by Hydration of Alkenes
  • Alkyne Acidity
  • Synthesis of Alcohols from Haloalkanes
  • Synthesis of amides from carboxylic acids
  • Addition of Hydrogen Halides to Alkynes
  • Alkene Epoxidation
  • Alkenes - Structure and Bond
  • HBr addition with peroxides
  • Alkenes
  • Cross or mixed aldol condensation
  • Acid-Base Properties of Amines
  • Structure and bonding of amines
  • Unimolecular elimination - E1
  • Alkene Stability
  • Cyclohexane
  • HX addition
  • Benzene - Protection and deprotection of the amino group
  • Conformations of Cyclohexane
  • Synthesis of Anhydrides from Carboxylic Acids
  • Hydroboration of Alkenes
  • Structure and bonding in ethers and epoxides
  • Cyclopropane
  • Halohydrin formation
  • Reaction of anhydrides with water
  • Substitution/elimination competition
  • Lactone Synthesis
  • Alkyne Ozonolysis
  • Synthesis of Alkenes by E2
  • Reduction of carboxylic acids to alcohols
  • Cyclobutane
  • Synthesis of alpha, beta-unsaturated carbonyls
  • Hofmann elimination

LATEST NEWS

  • Privacy Policy
  • Substituted cyclohexanes | 1,3-diaxial interaction
  • Conformational equilibrium in cyclohexane
  • Introduction to carbohydrates
  • Alkynes - Problem 12
  • Electrocyclic reactions
  • Photochemical reactions [2+2]
  • Intramolecular Diels-Alder reaction
  • Addition of bromine to conjugated dienes
  • Acid addition of halogens (HX) to conjugated dienes
  • Radical reactions in allylic systems
  • 1,4 elimination in allylic systems
  • SN2 prime in allylic systems
  • SN2 in allylic systems
  • Kinetic and thermodynamic control in allylic systems
  • Opening of cyclic ethers (epoxides)
  • Ethers as protecting groups of alcohols
  • Synthesis of ethers by SN1
  • Separation of enantiomers
  • Stereospecific and stereoselective reaction
  • Molecules with more than one chiral center
  • Stereochemistry of chemical reactions
  • Benzene - Problem 16
  • Azo coupling
  • Sandmeyer and Schiemann reactions
  • Claisen transposition
  • Birch reduction
  • Side chain oxidation
  • The benzylic position
  • Aromatic nucleophilic substitution by addition-elimination
  • Protection of activated positions
  • Reduction of nitro to amino and oxidation of amino to nitro
  • Synthesis of 1,2-dicarbonyl compounds
  • Synthesis of 1,3-dithianes
  • benzoin condensation
  • acyloinic condensation
  • Knoevenagel condensation
  • Michael's addition
  • Review of Claisen condensation
  • helical molecules
  • Rp and Sp notation in planes of chirality
  • Ra/Sa notation on chirality axes
  • R/S notation in stereogenic centers
  • Elements of asymmetry leading to chiral molecules
  • Elements of symmetry leading to achiral molecules
  • conformational analysis
  • Molecular structure
  • Phosphines and phosphorus ylides
  • Synthesis of 1,3-dithianes. UMPOLUNG reactions
  • Thioacetals, hydrolysis and reduction to alkanes
  • ylides of sulfur
  • Sulphoxide removal WITHOUT
  • The Thioethers
  • thiols
  • simulation of the infrared spectrum of propanamide
  • Simulation of the infrared spectrum of 1-butanamine
  • Simulation of the infrared spectrum of ethyl ethanoate
  • Simulation of the infrared spectrum of ethanoyl chloride
  • Simulation of the infrared spectrum of propanoic acid
  • Simulation of the infrared spectrum of ethanenitrile
  • Simulation of the infrared spectrum of diethyl ether
  • Simulation of the infrared spectrum of ethanal
  • Simulation of the infrared spectrum of 2-butanone
  • Simulation of the infrared spectrum of 1-propanol
  • Guareschi-Thorpe synthesis of pyridine
  • Kröhnke synthesis of pyridine
  • Pomerantz-Fritsch synthesis of isoquinolines
  • Pictet Spengler synthesis of isoquinoline
  • Bischer–Napieralski synthesis
  • Friedlander quinoline synthesis
  • Combes synthesis of quinolines
  • Alkyl and vinyl quinolines and isoquinolines
  • Nucleophilic substitution in quinoline and isoquinoline
  • Nucleophilic addition to quinolines and isoquinolines
  • Lithiation reaction in quinoline and isoquinoline
  • Electrophilic substitution by N-oxides
  • Electrophilic substitution reaction in quinoline and isoquinoline
  • Reactions with nitrogen lone pair: quinoline and isoquinoline
  • Reactivity of alkyl and vinyl pyridines
  • Nucleophilic substitution by elimination-addition: the pyridine
  • Nucleophilic substitution reactions in pyridine
  • Nucleophilic addition reactions to pyridines
  • pyridine lithiation
  • Electrophilic substitution at position 4 of pyridine
  • Synthesis of thiophene by 1,3-dipolar
  • Paal–Knorr synthesis of thiophene
  • Furan synthesis by 1,3-dipolar
  • Feist-Benary synthesis of furan
  • Paal–Knorr synthesis of furans
  • Synthesis of pyrrole via 1,3-dipolar
  • Hantzch synthesis of pyrrole
  • Paal–Knorr synthesis of pyrrole
  • furan opening
  • Derivatives of pyrrole, thiophene and furan
  • Cycloaddition reactions in furan
  • Lithiation reaction
  • Nucleophilic substitution in pyrrole, thiophene and furan
  • nucleophilic addition
  • Electrophilic substitution on thiophene
  • Sulfonation, formylation, Mannich and acetylation of furan
We use cookies

We use cookies on our website. Some of them are essential for the operation of the site, while others help us to improve this site and the user experience (tracking cookies). You can decide for yourself whether you want to allow cookies or not. Please note that if you reject them, you may not be able to use all the functionalities of the site.

Ok Decline
More information