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- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Reactions/Organic_Reactions/Preparation_of_Aliphatic_Fluorine_Compounds
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Reactions/Organic_Reactions/Preparation_of_Unsymmetrical_Biaryls_by_the_Diazo_Reaction_and_the_Nitrosoacetylamine_ReactionPreparation of Unsymmetrical Biaryls by the Diazo Reaction and the Nitrosoacetylamine reaction is an aryl-aryl coupling reaction via a diazonium salt. It is also known as the Gomberg–Bachmann reactio...Preparation of Unsymmetrical Biaryls by the Diazo Reaction and the Nitrosoacetylamine reaction is an aryl-aryl coupling reaction via a diazonium salt. It is also known as the Gomberg–Bachmann reaction.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Reactions/Organic_Reactions/Jacobsen_RearrangementThe Jacobsen rearrangement is a chemical reaction, commonly described as the migration of an alkyl group in a sulfonic acid derived from a polyalkyl- or polyhalobenzene
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Reactions/Organic_Reactions/Clemmensen_ReductionClemmensen reduction is a chemical reaction described as a reduction of carbonyls to alkanes using zinc amalgam and hydrochloric acid.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Reactions/Organic_Reactions/Clemmensen_Reduction/Reformatsky_ReactionThe Reformatsky reaction (sometimes spelled Reformatskii reaction) is an organic reaction which condenses aldehydes or ketones, with α-halo esters, using a metallic zinc to form β-hydroxy-esters.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Reactions/Organic_Reactions/Wacker_OxidationThe Wacker oxidation refers generally to the transformation of a terminal or 1,2-disubstituted alkene to a ketone through the action of catalytic palladium(II), water, and a co-oxidant.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Reactions/Organic_Reactions/Clemmensen_Reduction/Arndt-Eister_reactionThe Arndt–Eistert synthesis is a series of chemical reactions designed to convert a carboxylic acid to a higher carboxylic acid homologue (i.e. contains one additional carbon atom) and is considered a...The Arndt–Eistert synthesis is a series of chemical reactions designed to convert a carboxylic acid to a higher carboxylic acid homologue (i.e. contains one additional carbon atom) and is considered a homologation process.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Reactions/Organic_Reactions/Claisen_Condensation/Perkin_Reaction/Elbs_Reaction/Bucherer_reactionThe Bucherer reaction in organic chemistry is the reversible conversion of a naphthol to a naphthylamine in the presence of ammonia and sodium bisulfite. The reaction is widely used in the synthesis o...The Bucherer reaction in organic chemistry is the reversible conversion of a naphthol to a naphthylamine in the presence of ammonia and sodium bisulfite. The reaction is widely used in the synthesis of dye precursors aminonaphthalenesulfonic acids.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Reactions/Organic_Reactions/Hydroamination_Reactions_of_AlkenesHydroamination reactions of alkenes represent additions of N-H bonds across carbon-carbon double bonds. Viable substrates for these reactions include unactivated alkenes, vinyl arenes, allenes, and st...Hydroamination reactions of alkenes represent additions of N-H bonds across carbon-carbon double bonds. Viable substrates for these reactions include unactivated alkenes, vinyl arenes, allenes, and strained alkenes. The scope of the nitrogen-containing reactant includes amines, azoles, and N-protected substrates. A variety of catalysts have been employed including alkali metals, alkaline earth metals, transition metals, and lanthanides.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Reactions/Organic_Reactions/Dieckmann_CondensationThe Dieckmann condensation is the intramolecular chemical reaction of diesters with base to give β-ketoesters. It is named after the German chemist Walter Dieckmann (1869–1925). The equivalent intermo...The Dieckmann condensation is the intramolecular chemical reaction of diesters with base to give β-ketoesters. It is named after the German chemist Walter Dieckmann (1869–1925). The equivalent intermolecular reaction is the Claisen condensation.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Reactions/Organic_Reactions/Clemmensen_Reduction/Chichibabin_ReactionThe Chichibabin reaction is a method for producing 2-aminopyridine derivatives by the reaction of pyridine with sodium amide.
