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Organic Chemistry Book
Organic Nomenclature Book
THE MOST READ
- WHAT DOES ORGANIC CHEMISTRY STUDY?
- THE ORIGIN OF ORGANIC CHEMISTRY
- ORGANIC SYNTHESIS
- Bulletin No. 4
- MOLECULAR EDITORS
- MOLECULAR MODELS
- pKas LIST
- Alkanes nomenclature
- What is the importance of organic chemistry in the work of the petroleum engineer?
- Isomer classification
- ORGANIC CHEMISTRY I COURSE
- ORGANIC CHEMISTRY FORUM
- Physical properties of alkanes
- ADVANCED ORGANIC COURSE
- ORGANIC CHEMISTRY II COURSE
- Geometric or cis-trans isomers
- Types of hydrocarbons
- STRUCTURAL DETERMINATION
- Ester Nomenclature
- Aldehyde and Ketone Nomenclature
- Molecular Model - Ethanoic (Acetic) Acid
- isomeric alkanes
- University Course - ORGANIC I
- Molecular Model - Ethanedioic (oxalic) Acid
- The 20 amino acids that make up proteins
- Alkene Nomenclature
- Molecular Model - Methanoic (Formic) Acid
- Alcohol Nomenclature
- Alkanes
- chloroethanoic acid
- Alcohols - general characteristics
- Physical properties of ethers
- Molecular Model - Bromoethanoic Acid
- Molecular Model - Aminoethanoic Acid
- Cookies policy
- anti butane
- Butane-gauche
- Alcohol oxidation
- Molecular Model - Fluorethanoic Acid
- Molecular Model - Iodoethanoic Acid
- butane without
- Cycloalkanes nomenclature
- ANDROID APPS
- Molecular chirality and enantiomers
- Aldehydes and Ketones: Problem 4
- Benzene nomenclature
- organic chemistry books
- Anhydride Nomenclature
- Amino Acids - Isoelectric Point
- Physical properties of Alkynes
- Youtube Channel - Organic Chemistry
- Newman projection
- Preparation of aldehydes and ketones
- Amine Nomenclature
- Synthesis of Carboxylic Acids
- Alkene Hydration
- Nomenclature - Carboxylic Acids
- optical activity
- Physical Properties of Alkenes
- Alkenes hydrogenation
- Fisher projection
- 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
- Amide Nomenclature
- Acidity and basicity of alcohols
- Conformational analysis of ethane
- Electrophilic addition reactions
- Physical Properties of Carboxylic Acids
- Stereochemistry - Stereoisomerism
- Synthesis of esters from carboxylic acids - Esterification
- aldol condensation
- Alkyne nomenclature
- Isomers with a single asymmetric carbon
- Basic hydrolysis of esters. saponification
- Acid hydrolysis of esters
- Williamson's synthesis of ethers
- Alkanes - Problem 7
- Alkanes - Problem 4
- Haloform (Iodoform) reaction
- halogenation of benzene
- Elemental Analysis
- Synthesis of ethers by condensation of alcohols
- Ethers - epoxides nomenclature
- Symmetry in Chiral Molecules: Meso Forms
- Aldehydes and Ketones: Problem 10
- Markovnikov Rule - Regioselectivity
- alkynes
- Halogenation of Alkynes
- Morrison and Boyd
- Synthesis of Alcohols by reduction of carbonyls
- Alkene polymerization
- RS Notation on Fischer Projection
- Halogen addition
- Calculation of empirical and molecular formulas
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LATEST NEWS
- 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
- Madelung synthesis of indole
- Fisher's synthesis of indole
- Indole ring reduction
- Indole ring expansion
- Indole derivatives
- Electrophilic substitution with position 3 of the indole occupied
- Electrophilic substitution at the indole
- indole acidity
- Examples of fused heterocycle nomenclature
- Literation of the base heterocycle and numbering of the annex
- Peripheral numbering of the global heterocycle
- Rules for the choice of the base component
- General concepts of condensed heterocycle nomenclature
- General characteristics of diazines
- Cyclization of carbenes nitrenes and radicals
- Cyclization on sp carbons
- Cyclization processes by nucleophilic addition and addition-elimination at sp¹²2 carbons
- Formation of cycles through S$_N$2
- Classification of nucleophilic attacks (Baldwin's Rules)
- Reactants in cyclization reactions
- Synthesis of heterocycles by cyclization reactions
- The anomeric effect