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- Beckmann_rearrangement abstract "The Beckmann rearrangement, named after the German chemist Ernst Otto Beckmann (1853–1923), is an acid-catalyzed rearrangement of an oxime to an amide. Cyclic oximes yield lactams.This example reaction starting with cyclohexanone, forming the reaction intermediate cyclohexanone oxime and resulting in caprolactam is one of the most important applications of the Beckmann rearrangement, as caprolactam is the feedstock in the production of Nylon 6. The Beckmann solution consists of acetic acid, hydrochloric acid and acetic anhydride, and was widely used to catalyze the rearrangement. Other acids, such as sulfuric acid or polyphosphoric acid, can also be used. sulfuric acid is the most commonly used acid for commercial lactam production due to its formation of an ammonium sulfate by-product when neutralized with ammonia. Ammonium sulfate is a common agricultural fertilizer providing nitrogen and sulfur.".
- Beckmann_rearrangement thumbnail BeckmannRearrangement3.svg?width=300.
- Beckmann_rearrangement wikiPageExternalLink File:B_U_2_startAnimGif.gif.
- Beckmann_rearrangement wikiPageExternalLink File:B_U_startAnimGif.gif.
- Beckmann_rearrangement wikiPageID "251569".
- Beckmann_rearrangement wikiPageRevisionID "606046282".
- Beckmann_rearrangement hasPhotoCollection Beckmann_rearrangement.
- Beckmann_rearrangement subject Category:Name_reactions.
- Beckmann_rearrangement subject Category:Rearrangement_reactions.
- Beckmann_rearrangement type ChemicalProcess113446390.
- Beckmann_rearrangement type ChemicalReaction113447361.
- Beckmann_rearrangement type NameReactions.
- Beckmann_rearrangement type NaturalProcess113518963.
- Beckmann_rearrangement type PhysicalEntity100001930.
- Beckmann_rearrangement type Process100029677.
- Beckmann_rearrangement type RearrangementReactions.
- Beckmann_rearrangement comment "The Beckmann rearrangement, named after the German chemist Ernst Otto Beckmann (1853–1923), is an acid-catalyzed rearrangement of an oxime to an amide. Cyclic oximes yield lactams.This example reaction starting with cyclohexanone, forming the reaction intermediate cyclohexanone oxime and resulting in caprolactam is one of the most important applications of the Beckmann rearrangement, as caprolactam is the feedstock in the production of Nylon 6.".
- Beckmann_rearrangement label "Beckmann rearrangement".
- Beckmann_rearrangement label "Beckmann-Umlagerung".
- Beckmann_rearrangement label "Beckmann-omlegging".
- Beckmann_rearrangement label "Przegrupowanie Beckmanna".
- Beckmann_rearrangement label "Rearranjo de Beckmann".
- Beckmann_rearrangement label "Réarrangement de Beckmann".
- Beckmann_rearrangement label "Transposición de Beckmann".
- Beckmann_rearrangement label "Перегруппировка Бекмана".
- Beckmann_rearrangement label "ベックマン転位".
- Beckmann_rearrangement label "贝克曼重排反应".
- Beckmann_rearrangement sameAs Beckmann-Umlagerung.
- Beckmann_rearrangement sameAs Transposición_de_Beckmann.
- Beckmann_rearrangement sameAs Réarrangement_de_Beckmann.
- Beckmann_rearrangement sameAs ベックマン転位.
- Beckmann_rearrangement sameAs Beckmann-omlegging.
- Beckmann_rearrangement sameAs Przegrupowanie_Beckmanna.
- Beckmann_rearrangement sameAs Rearranjo_de_Beckmann.
- Beckmann_rearrangement sameAs m.01lbl0.
- Beckmann_rearrangement sameAs Q813746.
- Beckmann_rearrangement sameAs Q813746.
- Beckmann_rearrangement sameAs Beckmann_rearrangement.
- Beckmann_rearrangement wasDerivedFrom Beckmann_rearrangement?oldid=606046282.
- Beckmann_rearrangement depiction BeckmannRearrangement3.svg.
- Beckmann_rearrangement isPrimaryTopicOf Beckmann_rearrangement.
