PREFERRED TERM
organic chemistry
TYPE
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
NARROWER CONCEPTS
RELATED CONCEPTS
- 1,2-addition
- 1,4-addition
- acetal formation
- acetates
- acetoacetic ester alkylation
- acetoacetic ester
- achiral
- acid anhydrides alcoholysis
- acid anhydrides
- acid-catalyzed cleavage
- acid chlorides alcoholysis
- acid chlorides
- acid derivatives
- acidity of phenols
- acids
- active metals
- acyl aromatic substitution
- acylation
- addition of alcohols
- addition of carbanions
- addition of cyanide
- addition of Grignard reagent
- addition of halogens
- addition of hydrogen
- addition of organozinc compounds
- alcohols
- alcoholysis
- aldehydes
- aldol condensation
- alfa-halo acids
- aliphatic acids
- aliphatic substitution
- alkali fusion
- alkanes
- alkenes
- alkoxymercuration-demercuration
- alkylation
- alkylbenzenes
- alkyl dihalides
- alkyl group
- alkyl halides
- alkynes
- alkynes preparation
- allylic substitution
- alpha-halogenation
- amination
- amine group
- amines alkylation
- amines
- amino acids
- ammonia derivatives
- ammonia
- ammonolysis
- ammonolysis of esters
- amonnium salts
- anhydrides
- anionic polymerization
- anti-aromaticity
- arenes
- aromatic acids
- aromatic compounds
- aromaticity
- aryl group
- aryl halides
- Barbier method
- base-catalyzed cleavage
- basicity of amines
- biomolecules
- Cannizzaro reaction
- carbanions
- carbenes
- carbocations
- carbohydrates
- carbonation
- carbon chain lengthening
- carboxylic acids
- cationic polymerization
- chain degradation
- chemical characteristics
- chemical reduction
- chiral center
- chirality
- chromatography
- claisen condensation
- cleavage by acids
- Clemmensen reduction
- click chemistry
- combustion
- combustion reaction
- configuration
- conjugated dienes
- conjugation
- coordination polymerization
- copolymerization
- coupling
- cracking
- cumulated dienes
- cyanohydrin formation
- decarboxylation
- dehalogenation
- dehydration
- dehydration of alcohols
- dehydrohalogenation
- derivatization
- detergents
- diazo coupling
- diazonium salts
- dienes
- distillation column
- dyes
- electrophilic aromatic substitution
- elemental analysis
- empirical formula
- enamine formation
- enediol formation
- epimerization
- epoxides
- ester formation
- esters alcoholysis
- esters
- ether formation
- ethers
- extraction
- fats
- Fischer projection
- formation of aldehyde
- formation of glycoside
- formation of Grignard reagent
- formation of ketone
- formation of metal acetylides
- formation of peptides
- free radical
- free-radical polymerization
- Friedel-Crafts acylation
- Friedel-Crafts alkylation
- fuel
- functional derivatives
- functional group characterization
- functional group
- Gabriel phthalimide synthesis
- glycerides
- glycol formation
- Grignard reagent
- grignard synthesis
- halide exchange
- halides
- haloform reaction
- halogenation
- halohydrin formation
- halohydrins
- heterocyclic compounds
- Hinsberg test
- Hofmann degradation
- hofmann elimination
- Huckel's rule
- hybridization
- hydration(chemical reaction)
- hydroboration
- hydrocarbons
- hydrogenation
- hydrogen halides
- hydrogenolysis
- hydrolysis
- hydrolysis of acid anhydrides
- hydrolysis of acid chlorides
- hydrolysis of amides
- hydrolysis of esters
- hydrolysis of fats
- hydrolysis of nitriles
- hydroxylation
- identification
- imine formation
- intermediates
- International Union of Pure and Applied Chemistry(IUPAC)
- inversion
- ionic polymerization
- isolated dienes
- isomers
- isoprenoid compounds
- IUPAC nomenclature
- ketones
- Kolbe reaction
- lactones
- leaving group
- malonic ester alkylation
- malonic ester
- metal acetylides
- methylbenzenes
- Michael Addition
- molecular dipole
- molecular formula
- molecular geometry
- natural compounds
- Newman projection
- nitration
- nitrosation
- nucleic acids
- nucleophilic addition
- nucleophilic aromatic substitution
- nucleophilic substitution
- optical activity
- organic acids
- organic compounds
- organic phosphates
- organic salts
- organic synthesis
- organoarsenic compounds
- organoboron compounds
- organocopper compounds acylation
- organometallic compounds
- organonitrogen compounds
- organophosphorus compounds
- organosilicon compounds
- organosulfur compounds
- osazone formation
- oxidation
- oxidation of carbohydrates
- oxidation of methyl ketones
- oxygen-containing organic compounds
- oxymercuration-demercuration
- oxymercuration
- ozonolysis
- periodic acid
- peroxidation
- phenols
- phosphines
- phosphonic acids
- phosphorus pentachloride
- phosphorus trichloride
- phosphorus trihalides
- phthalimidomalonic ester
- physical organic chemistry
- polymerization
- polymers
- preparation of acid chlorides
- preparation of alcohols
- preparation of alkanes
- preparation of alkenes
- preparation of alkyl halides
- preparation of amides
- preparation of amines
- preparation of amino acids
- preparation of aryl halides
- preparation of carboxylic acids
- preparation of epoxids
- preparation of esters
- preparation of ethers
- preparation of Grignard reagent
- preparation of ketones
- preparation of phenols
- primary alcohols
- primary alky halides
- propionates
- protecting group
- protection of functional group
- protonation
- reaction conditions
- rearrangement
- recrystallization
- reduction of acids
- reduction of alkynes
- reduction of carbohydrates
- reduction of esters
- reduction of nitriles
- reductive amination
- reductive deamination
- reformatsky reaction
- regioselectivity
- Reimer-Tiemann reaction
- replacement of nitrogen
- resonance
- ring substitution
- Ruff degradation
- salt formation
- secondary alcohols
- self-assembled monolayer
- separation
- solvent effect
- solvent selection
- spectral characteristics
- spectrometry
- stereochemistry
- stereoisomers
- stereoselectivity
- steric hindrance
- structural formula
- sublimation
- sulfonation
- sulfuric acid
- surfactants
- thionyl chloride
- transesterification
- Untranslated Term
- vicinal dihalides
- volatile organic compounds
- Williamson synthesis
- Wittig reaction
- Wolff-Kishner reduction
IN OTHER LANGUAGES
شیمی آلی
Persian
URI
http://www.irandoc.acir/onto/irandoc/CHEM0001883