Amyl alcohol |
Outline of chemistry |
Electron counting |
Ketene |
International Numbering System for Food Additives |
Polyatomic ion |
List of synthetic polymers |
Cyanoacrylate |
Rotaxane |
Disulfide bond |
Fourier transform spectroscopy |
Alexander Shulgin |
Disulfide |
Mesomeric effect |
Chemisorption |
PH indicator |
Hemiacetal |
Size-exclusion chromatography |
Pyrophosphate |
Pierre Louis Dulong |
X-ray scattering techniques |
Magnetic stirrer |
Jean Stas |
Organic Reactions |
Sharpless epoxidation |
Swern oxidation |
Sharpless asymmetric dihydroxylation |
Pinner reaction |
Carl Auer von Welsbach |
Transesterification |
Decarboxylation |
Molecular dynamics |
Ice XII |
Relative atomic mass |
Thioether |
Index of chemistry articles |
Meniscus (liquid) |
Charles Coulson |
Molality |
Marsh test |
Standard state |
Halogen addition reaction |
Halohydrin formation reaction |
Outline of organic chemistry |
SN2 reaction |
Alkadiene |
Cumene process |
Scientific instrument |
Color of chemicals |
Glyceride |
Friedrich Accum |
Open-chain compound |
Oleochemical |
Backbone chain |
Ring-opening polymerization |
Chemometrics |
Bayer process |
Boris Pavlovich Belousov |
Robert Havemann |
Self-ionization of water |
Common-ion effect |
Phthalate |
Imino acid |
Absorption spectroscopy |
Oxyanion |
Isothiocyanate |
Irreducible representation |
Silanol |
Andreas Libavius |
Hydroxylation |
Acryloyl group |
Slater-type orbital |
Gaussian orbital |
Coupled cluster |
Tetranortriterpenoid |
Noble gas compound |
Organic geochemistry |
Potential gradient |
Hund's rule of maximum multiplicity |
Sulfite |
Alfred J. Lotka |
Williamson ether synthesis |
Assay |
Aldol |
Aldol condensation |
Royal Society of Chemistry |
Phosphodiester bond |
Ylide |
Intersystem crossing |
Chrome plating |
Nucleophilic addition |
Tosyl |
Sulfonate |
Mutarotation |
Rotational spectroscopy |
Fluorophore |
Open shell |
F-center |
Phosphite |
List of chemical compounds with unusual names |
Cyanohydrin |
Antimonite |
Malonate |
Laboratory information management system |
Titration curve |
Acyl chloride |
Lodewijk van den Berg |
Chemical Abstracts Service |
Leblanc process |
Freezing-point depression |
Lead glass |
Polyoxometalate |
Liposome |
Alnico |
Aryl halide |
Electrophilic substitution |
Reactivity series |
List of alchemists |
Thermochemical equation |
Girdler sulfide process |
Brasso |
Polyacetylene |
Molecular modelling |
Vladimir Ipatieff |
Free-radical addition |
Raschig process |
Bosch reaction |
Semisynthesis |
Total synthesis |
Acidic oxide |
Polybrominated diphenyl ethers |
Biogeochemistry |
Halomethane |
Electrophilic aromatic directing groups |
Effervescence |
Imide |
Colloidal gold |
Paraben |
Total analysis system |
List of interstellar and circumstellar molecules |
George C. Pimentel |
Edman degradation |
Ellen Swallow Richards |
Reductive dechlorination |
Analytical technique |
Burton process |
Deacon process |
Thiocyanate |
Nikolay Beketov |
Nikolay Zelinsky |
Ammonium sulfate precipitation |
Casomorphin |
Cuprate |
George Kistiakowsky |
Charles-Adolphe Wurtz |
Bisulfide |
Fischer indole synthesis |
Cyclopentadienyl complex |
Cyclic voltammetry |
Kinetic isotope effect |
Diarylethene |
Ionic liquid |
Cope reaction |
Photoisomerization |
Charge-transfer complex |
Zeta potential |
Molecular recognition |
Kraft process |
Dangling bond |
Superhard material |
Contact process |
Bell metal |
Pseudohalogen |
Coulometry |
Qualitative inorganic analysis |
Free-radical halogenation |
Trifluoromethanesulfonate |
Stille reaction |
Suzuki reaction |
Polyelectrolyte |
Chemical shift |
Harold Warris Thompson |
Capillary electrophoresis |
William de Wiveleslie Abney |
Ligand field theory |
Carboxamide |
Intermetallic |
Cyclodextrin |
Relativistic quantum chemistry |
Silylene |
Sigmatropic reaction |
Group transfer reaction |
Ene reaction |
Peptide synthesis |
Aldaric acid |
Diazo |
Reaction coordinate |
Isopropyl |
Radical substitution |
Bernard Courtois |
Sonogashira coupling |
Methoxy group |
Organochloride |
Thio- |
Solid-phase synthesis |
NWChem |
Toxic Substances Control Act of 1976 |
Carbonatation |
Single bond |
Sabatier reaction |
Energy harvesting |
Isolobal principle |
Tollens' reagent |
Dication |
Heterogeneous catalysis |
Homogeneous catalysis |
Clara Immerwahr |
Reference electrode |
Trihalomethane |
Carbo-mer |
Chemical file format |
Formate |
Cope rearrangement |
Stereospecificity |
Stereoselectivity |
Frasch process |
Aryne |
Polysulfide |
Appel reaction |
Absorption band |
Lead chamber process |
Oxygen scavenger |
Material properties of diamond |
Conversion (chemistry) |
Accelerant |
Hermann von Fehling |
Hofmann rearrangement |
Chemical test |
Iodine test |
Risk and Safety Statements |
Hunter process |
Kroll process |
List of inorganic compounds |
Amperometric titration |
Strain energy |
Ozonolysis |
Betts electrolytic process |
Parkes process |
Glass tube |
Reductive elimination |
Oxidative addition |
Tetravalence |
Trigonal pyramidal molecular geometry |
Nitrogen inversion |
Galactomannan |
Protic solvent |
Robinson annulation |
Initiation (chemistry) |
Electrophilic halogenation |
Fenton's reagent |
Peroxyacyl nitrates |
Hydrogen halide |
Kolbe electrolysis |
Van der Waals strain |
Chemical biology |
Hydrometallurgy |
Carbon in pulp |
Petroleum geochemistry |
Carbenoid |
Intercalation (chemistry) |
Convergent synthesis |
Divergent synthesis |
One-pot synthesis |
Microwave chemistry |
Walden inversion |
Chiral pool synthesis |
Photocatalysis |
Retrosynthetic analysis |
Buffering agent |
Formal charge |
Permanganate |
Gabriel synthesis |
Hofmann elimination |
Non-coordinating anion |
Alkyl cycloalkane |
Comproportionation |
Atom economy |
Mass-independent fractionation |
Acid salt |
Fatty alcohol |
1,2-rearrangement |
Gamma spectroscopy |
Alkyne trimerisation |
Passerini reaction |
Self-assembled monolayer |
Journal of the American Chemical Society |
Multi-component reaction |
Mannich reaction |
Carl Mannich |
Betaine |
Knoevenagel condensation |
Self-condensation |
Enone |
Synthon |
Amidine |
Lipid A |
Step-growth polymerization |
Organopalladium |
Fischer oxazole synthesis |
Sandmeyer reaction |
Fabric softener |
Karen Wetterhahn |
Polar bond |
Kilocalorie per mole |
Metalation |
Analytical balance |
Wacker process |
Specific rotation |
Enantiomeric excess |
Thermodynamic versus kinetic reaction control |
Allylic rearrangement |
Ferrier rearrangement |
IUPAC nomenclature for organic transformations |
Chemoselectivity |
Olefin metathesis |
Non-nucleophilic base |
Acyloin condensation |
Pummerer rearrangement |
Singlet oxygen |
Abundance (chemistry) |
Peroxy acid |
List of materials analysis methods |
Radical ion |
Derivatization |
Monsanto process |
Phosphide |
Phosphorus halide |
Total organic carbon |
Single-molecule magnet |
Radical polymerization |
Organosulfur compounds |
Calixarene |
Transition metal carbene complex |
Hiyama coupling |
Benzoin condensation |
Ring strain |
Alkyne metathesis |
Chiral ligand |
Oxidative coupling |
Planar chirality |
Axial chirality |
Bouveault aldehyde synthesis |
Electronic correlation |
Gewald reaction |
Nitroaldol reaction |
Oxycation |
Manganate |
Acid catalysis |
Nitrosation |
Multi-configurational self-consistent field |
Carbodiimide |
Cheletropic reaction |
Phosphoric acids and phosphates |
Criegee rearrangement |
Wiswesser's rule |
Alkane metathesis |
Organic redox reaction |
Carboxylate |
One-electron reduction |
Electron transfer |
Steady state (chemistry) |
Banert cascade |
Basis set (chemistry) |
Iodate |
Periodate |
Cascade reaction |
Perbromate |
Pyrimidinedione |
Lanthanide contraction |
Homochirality |
Avoided crossing |
Dicarboxylic acid |
Periodinane |
Silicide |
Boiling-point elevation |
Carl Remigius Fresenius |
Pine oil |
Aromatization |
Alkyl phosphate |
Tishchenko reaction |
Saran (plastic) |
Detailed balance |
Ullmann reaction |
Ullmann condensation |
Austin Model 1 |
Staudinger reaction |
Shock sensitivity |
Martinet dioxindole synthesis |
Selenate |
Reissert indole synthesis |
Tellurate |
Eilhard Mitscherlich |
Ether lipid |
Coordination geometry |
Endohedral fullerene |
Mixed oxide |
Salt bridge |
Prochirality |
Gassman indole synthesis |
Household chemicals |
Sulfonium |
Hemetsberger indole synthesis |
Borderline hydrides |
Beta-Hydride elimination |
Tungstate |
Macrocycle |
Barbier reaction |
Dow Corning |
Nenitzescu indole synthesis |
Mulliken population analysis |
Free-radical reaction |
Hermann Wilhelm Vogel |
Internal conversion (chemistry) |
Bond dipole moment |
Polymer science |
Aromatic sulfonation |
Cyanohydrin reaction |
Pechmann condensation |
Enthalpy of atomization |
Nucleophilic aromatic substitution |
Voltammetry |
Matrix isolation |
Molecular electronic transition |
Moses Gomberg |
Skraup reaction |
Hexavalent chromium |
Homoleptic |
Catalytic cycle |
Menshutkin reaction |
Biocatalysis |
Triiodide |
Angewandte Chemie |
Octene |
Ida Noddack |
Azo coupling |
Catalytic triad |
Microemulsion |
Duff reaction |
Iminium |
Formylation reaction |
Bergius process |
Atropisomer |
Detection limit |
Carroll rearrangement |
Ionic strength |
Endo-exo isomerism |
Natural material |
Alexander Dianin |
Ash (analytical chemistry) |
Overman rearrangement |
Laundry detergent |
Zerewitinoff determination |
Pidgeon process |
Silicothermic reaction |
Aluminothermic reaction |
Calciothermic reaction |
Reformatsky reaction |
SNi |
Biginelli reaction |
Hyperconjugation |
Prelog strain |
Peukert's law |
Cumulene |
Polyyne |
Ferricyanide |
Ferrocyanide |
Schiff test |
R-410A |
Fries rearrangement |
Nucleophilic acyl substitution |
Osmotic concentration |
Atoms in molecules |
Square planar molecular geometry |
Geminal halide hydrolysis |
Ineos |
Shapiro reaction |
Chiral auxiliary |
Bisulfite |
Triplet oxygen |
Ferrate(VI) |
Iodine clock reaction |
Adipate |
Chemical clock |
Tartrate |
Radiolysis |
IUPAC numerical multiplier |
Force field (chemistry) |
Povarov reaction |
Nicolaou Taxol total synthesis |
Thioketone |
Theodor Curtius |
Van Deemter equation |
Chemische Berichte |
Tetrahedron (journal) |
Cyanocarbon |
Cyclophane |
Bead test |
McMurry reaction |
Heteropoly acid |
Modern valence bond theory |
Journal of the Chemical Society |
E1cB-elimination reaction |
Organoselenium chemistry |
Measurement uncertainty |
Strecker amino acid synthesis |
Reissert reaction |
Radiation chemistry |
Ring-closing metathesis |
Reed reaction |
Alkylimino-de-oxo-bisubstitution |
Bredt's rule |
Spectator ion |
Autoxidation |
Organic Letters |
Jacobsen epoxidation |
Pauling's rules |
Photodegradation |
Ring expansion and ring contraction |
Favorskii rearrangement |
Isotope dilution |
Tetrahedron Letters |
Peterson olefination |
Nanomaterial-based catalyst |
Intergranular corrosion |
Annulyne |
Edward Weston (chemist) |
Weinreb ketone synthesis |
Divalent |
Grieco elimination |
Azomethine ylide |
Prato reaction |
Bamberger rearrangement |
Stepwise reaction |
Michael J. S. Dewar |
Microscopic reversibility |
Marcus theory |
Flammability limit |
Persistent carbene |
Hydrazone iodination |
Ketenimine |
Carbenium ion |
Arenium ion |
Carbonate ester |
Dean-Stark apparatus |
Trans effect |
Solubility chart |
Water-reactive |
Charge number |
Endohedral hydrogen fullerene |
Petasis reaction |
Polarography |
Graphite intercalation compound |
Perkow reaction |
Electroextraction |
List of chemistry journals |
Neighbouring group participation |
Acyloin |
Otto Lehmann (physicist) |
Chan rearrangement |
Chemical law |
Aza- |
Uranyl |
Ellingham diagram |
Combustion analysis |
Photoswitch |
Molecular configuration |
Brook rearrangement |
Umpolung |
Colored fire |
Ring flip |
Hand sanitizer |
Bent's rule |
2-Norbornyl cation |
Dieckmann condensation |
Blaise ketone synthesis |
Dakin oxidation |
Shi epoxidation |
Paclitaxel total synthesis |
Anomeric effect |
Spectrochemical series |
Pinacol rearrangement |
Non-stoichiometric compound |
Isodesmic reaction |
Pyrone |
Chemical garden |
Carcerand |
Vanadate |
Mond process |
Hunsdiecker reaction |
Lossen rearrangement |
Tributyltin |
International Chemical Safety Cards |
Bergman cyclization |
Diradical |
Glycol cleavage |
Demjanov rearrangement |
Hammond's postulate |
Bartoli indole synthesis |
Prins reaction |
Oxygen transmission rate |
Pyrylium salt |
Dissolved organic carbon |
Overpotential |
Gauche effect |
Organosilicon |
Organophosphorus compound |
Trispyrazolylborate |
Benzilic acid rearrangement |
Frost diagram |
Tetrafluoroborate |
ACS style |
Chromate conversion coating |
Orthoester |
GAMESS (US) |
Aromatic ring current |
Homoaromaticity |
Darzens reaction |
Hans Freeman |
Raphael Meldola |
CHN analyzer |
Stetter reaction |
Polar effect |
Solvated electron |
Lowry protein assay |
Britton Chance |
Methanium |
Monte Carlo molecular modeling |
Hazardous Materials Identification System |
Gattermann reaction |
Degree of unsaturation |
List of boiling and freezing information of solvents |
Alkali salt |
Ab initio quantum chemistry methods |
Directed ortho metalation |
Finkelstein reaction |
Basic oxide |
Coordination polymer |
Geminal |
List of extremely hazardous substances |
Diprotic acid |
Robert Mond |
Molecular logic gate |
Dispersion (chemistry) |
Transfer hydrogenation |
Norrish reaction |
Asymmetric induction |
Button cell |
Tert-Butyloxycarbonyl protecting group |
Structure factor |
Von Braun amide degradation |
Molecular graphics |
Chemistry: A European Journal |
Bulletin of the Chemical Society of Japan |
Journal of Chemical Physics |
Journal of Biological Chemistry |
Coordination sphere |
Hammett equation |
Bridging ligand |
Malonic ester synthesis |
Topicity |
Nazarov cyclization reaction |
Cofiring |
Journal of the American Society for Mass Spectrometry |
Internal standard |
Deamidation |
Grob fragmentation |
18-electron rule |
List of food additives |
Auwers synthesis |
Anna J. Harrison |
Phosphine oxide |
Shell higher olefin process |
Courtaulds |
Alkyl nitrites |
List of refrigerants |
Gibbs isotherm |
Organomercury |
Semicarbazone |
Dehydrohalogenation |
Antarafacial and suprafacial |
Bancroft rule |
Cyclopropanation |
Principle (chemistry) |
Ring-opening metathesis polymerisation |
Meisenheimer complex |
Kinetic resolution |
Herz reaction |
Scholl reaction |
Bridged compounds |
Sugar acid |
Indole alkaloid |
Corrinoid |
Chiral derivatizing agent |
Thioxanthene |
Stevens rearrangement |
Side reaction |
Jacobsen rearrangement |
Behavior of nuclear fuel during a reactor accident |
Organogermanium compound |
Negishi coupling |
Sulfinic acid |
Borohydride |
Oxazines |
Benzhydryl compounds |
Benzylidene compounds |
Organozinc compound |
Organocadmium compound |
Chemical state |
Transmetalation |
Fractional crystallization (chemistry) |
Niementowski quinazoline synthesis |
Chloroalkyl ether |
Benzocycloheptene |
Cholestene |
Bucherer reaction |
Organolead compound |
Onium compound |
Monoterpene |
Leuckart reaction |
Liebigs Annalen |
Enyne metathesis |
Organofluorine chemistry |
Solubility table |
Crude oil assay |
Semipinacol rearrangement |
Joseph W. Kennedy |
Blanc chloromethylation |
Reaction calorimeter |
Electrosynthesis |
Metal nitrosyl complex |
Hercules Inc. |
Oxon (chemical) |
Oppenauer oxidation |
Arrow poison |
Leveling effect |
Ethynyl radical |
Aldonic acid |
Elbs persulfate oxidation |
Edward Schunck |
Organocopper compound |
Woodward cis-hydroxylation |
List of battery types |
Cyclopentadienyl anion |
Radical-nucleophilic aromatic substitution |
Journal of Materials Chemistry |
Salimuzzaman Siddiqui |
ZINC database |
Hammick reaction |
Alpha cleavage |
Carboxybenzyl |
Exploding trousers |
Acetoxy group |
Desymmetrization |
Schlenk line |
Molecular Hamiltonian |
Covalent radius of fluorine |
Steven V. Ley |
List of commonly available chemicals |
Hammett acidity function |
Thorpe reaction |
Rubottom oxidation |
Fischer glycosidation |
Guerbet reaction |
Chiral resolution |
Eschenmoser fragmentation |
Phosphazene |
Sulfenic acid |
Captodative effect |
Lanthanide trifluoromethanesulfonates |
Tricyclic |
Ruzicka large-ring synthesis |
National Historic Chemical Landmarks |
Absolute configuration |
Lab on a Chip (journal) |
Elizabeth Ann Nalley |
Atomic ratio |
Heterocyclic amine |
Trifluoromethyl |
Amadori rearrangement |
Carbohydrate chemistry |
Nef reaction |
Nierenstein reaction |
NMR tube |
McLafferty rearrangement |
Etymology of chemistry |
Z-matrix (chemistry) |
Molecular solid |
Hydrosilylation |
Elbs reaction |
Osazone |
Oxidative decarboxylation |
Zincke nitration |
Nor- |
Allylic strain |
Ivar Karl Ugi |
COSHH |
Organocatalysis |
Reduction of nitro compounds |
Journal of the Royal Institute of Chemistry |
Whiting reaction |
Transition state analog |
CRC Handbook of Chemistry and Physics |
Asymmetric catalytic oxidation |
Mother liquor |
Wohl degradation |
Hayashi rearrangement |
Mukaiyama aldol addition |
Suspension polymerization |
Willgerodt rearrangement |
Nickel titanium |
Chromatography in blood processing |
Xylidine |
Organoaluminium chemistry |
Water model |
Mumm rearrangement |
Periodic trends |
ANRORC mechanism |
Chain transfer |
Vanadyl ion |
Charles Herty |
Ligand cone angle |
Franz Joseph Emil Fischer |
Ferrous metallurgy |
Peroxydisulfate |
Carbometalation |
Wallach rearrangement |
Wenker synthesis |
Dihydrogen complex |
Procyanidin |
Chemical Physics Letters |
Ferdinand Hurter |
Hydroamination |
Aqueous normal-phase chromatography |
Wender Taxol total synthesis |
Semi-rigid molecule |
Wagner-Jauregg reaction |
Coordination isomerism |
Hexacoordinate |
Tetracoordinate |
Oseltamivir total synthesis |
Carbazole |
Isoflavonoid |
Multicolumn countercurrent solvent gradient purification |
Hydron (chemistry) |
Wanzlick equilibrium |
Specificity constant |
DuPont Central Research |
Constraint algorithm |
Upjohn dihydroxylation |
Thallium halides |
Chemesthesis |
Quinine total synthesis |
Atomic carbon |
Kapustinskii equation |
Localized molecular orbitals |
Gallium halides |
Potentiometric titration |
Zintl phase |
Polyiodide |
Kulinkovich reaction |
Marker degradation |
J. R. Partington |
Arthur C. Cope |
Hans Meerwein |
Work-up (chemistry) |
Cooling bath |
Azeotrope tables |
Schmidt reaction |
Chain disproportionation |
Carbon label |
Pseudoproline |
Dose (biochemistry) |
Slater's rules |
Crotyl |
Hydrogenase mimic |
Meta- (chemistry) |
Oxidation of primary alcohols to carboxylic acids |
Group 2 organometallic chemistry |
Pendant group |
Oligonucleotide synthesis |
Kumada coupling |
Journal of Mass Spectrometry |
E-Z notation |
Mesoporous silica |
Proton affinity |
Acidity function |
Pierre Jean Robiquet |
Keggin structure |
Chemtura |
List of works by Joseph Priestley |
Indium chalcogenides |
Determination of equilibrium constants |
Encyclopedia of Reagents for Organic Synthesis |
Coprecipitation |
Atomic mass constant |
Artificial enzyme |
Molecular binding |
Tetrahalomethane |
STO-nG basis sets |
Ojima lactam |
Uma Chowdhry |
Chichibabin reaction |
Chichibabin pyridine synthesis |
Boord olefin synthesis |
Short-chain fatty acid |
Organonickel |
Tube furnace |
Di-pi-methane rearrangement |
Ei mechanism |
Equilibrium fractionation |
Alkyne zipper reaction |
Deoxidization |
Recueil des Travaux Chimiques des Pays-Bas |
Webster's reagent |
Bite angle |
Transition metal dinitrogen complex |
European Journal of Inorganic Chemistry |
Four-center two-electron bond |
Anselme Payen Award |
Low-barrier hydrogen bond |
Bisoxazoline ligand |
Alkali metal halide |
Moiety conservation |
ACS Chemical Biology |
Aluminium smelting |
High production volume chemicals |
Iodolactonization |
Free base |
Carl Schorlemmer |
Reaction dynamics |
Complex metal hydride |
CSA Trust |
Alkali hydroxide |
Karlsruhe Congress |
Occupational exposure limit |
Loparite-(Ce) |
Arthur C. Cope Award |
Alkyl sulfonate |
Organoarsenic chemistry |
Allopumiliotoxin |
List of chemical analysis methods |
Kowalski ester homologation |
Ludwig Gattermann |
Composition of the human body |
Cyanate ester |
Ate complex |
Bleaching of wood pulp |
Diffusion-controlled reaction |
Eduard Zintl |
Photoinitiator |
Asymmetric carbon |
Otto Ruff |
Cadet's fuming liquid |
Double layer (surface science) |
Sulfite process |
Heinz Gerischer |
Firefly (computer program) |
Mass attenuation coefficient |
Grundmann aldehyde synthesis |
Otto Folin |
Molar mass constant |
Woodward's rules |
Air-free technique |
George Ernest Gibson |
Hydrolysis constant |
Inorganic Syntheses |
Karl Theophil Fries |
Giacomo Luigi Ciamician |
CLP Regulation |
Kolbe nitrile synthesis |
Koch reaction |
Kochi reaction |
Working electrode |
Anodic stripping voltammetry |
Mesophase |
Energy profile (chemistry) |
Organozirconium chemistry |
Hydrometalation |
Curcuminoid |
Topological index |
Acetoacetic ester synthesis |
Allotropes of sulfur |
Max Bodenstein |
Surface diffusion |
Mukaiyama Taxol total synthesis |
Autoacceleration |
Black oxide |
Hybrid physical-chemical vapor deposition |
Allotropes of phosphorus |