![Beckmann rearrangement of cyclohexanone oxime in a microchemical system: The role of SO3 and product inhibition - Zhang - 2012 - AIChE Journal - Wiley Online Library Beckmann rearrangement of cyclohexanone oxime in a microchemical system: The role of SO3 and product inhibition - Zhang - 2012 - AIChE Journal - Wiley Online Library](https://aiche.onlinelibrary.wiley.com/cms/asset/c1956da5-a2e1-4fbf-97f4-2bd122d71756/mfig003.jpg)
Beckmann rearrangement of cyclohexanone oxime in a microchemical system: The role of SO3 and product inhibition - Zhang - 2012 - AIChE Journal - Wiley Online Library
![Application of an immobilized ionic liquid for the preparation of hydroxylamine via hydrolysis of cyclohexanone oxime - Wang - 2021 - Zeitschrift für anorganische und allgemeine Chemie - Wiley Online Library Application of an immobilized ionic liquid for the preparation of hydroxylamine via hydrolysis of cyclohexanone oxime - Wang - 2021 - Zeitschrift für anorganische und allgemeine Chemie - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/eccb4636-da8e-4004-b2da-c6f82e282a06/zaac202000370-toc-0001-m.jpg?trick=1675076316411)
Application of an immobilized ionic liquid for the preparation of hydroxylamine via hydrolysis of cyclohexanone oxime - Wang - 2021 - Zeitschrift für anorganische und allgemeine Chemie - Wiley Online Library
One pot synthesis of cyclohexanone oxime from nitrobenzene using a bifunctional catalyst - Chemical Communications (RSC Publishing)
![Beckmann Rearrangement of 15N-Cyclohexanone Oxime on Zeolites Silicalite-1, H-ZSM-5, and H-[B]ZSM-5 Studied by Solid-State NMR Spectroscopy | Journal of the American Chemical Society Beckmann Rearrangement of 15N-Cyclohexanone Oxime on Zeolites Silicalite-1, H-ZSM-5, and H-[B]ZSM-5 Studied by Solid-State NMR Spectroscopy | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja066392c/asset/images/large/ja066392cn00001.jpeg)
Beckmann Rearrangement of 15N-Cyclohexanone Oxime on Zeolites Silicalite-1, H-ZSM-5, and H-[B]ZSM-5 Studied by Solid-State NMR Spectroscopy | Journal of the American Chemical Society
![EXP Cyclohexanone Oxime and Its Rearrangement to -Caprolactam - Experiment 4 Cyclohexanone Oxime - Studocu EXP Cyclohexanone Oxime and Its Rearrangement to -Caprolactam - Experiment 4 Cyclohexanone Oxime - Studocu](https://d20ohkaloyme4g.cloudfront.net/img/document_thumbnails/089d959845349f47fdecd79e6baf6d37/thumb_1200_1697.png)
EXP Cyclohexanone Oxime and Its Rearrangement to -Caprolactam - Experiment 4 Cyclohexanone Oxime - Studocu
![Beckmann rearrangement over phosphotungstic acid/SiMCM-41 cyclohexanone oxime to ε-caprolactam - ScienceDirect Beckmann rearrangement over phosphotungstic acid/SiMCM-41 cyclohexanone oxime to ε-caprolactam - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0926860X03001820-fx1.gif)
Beckmann rearrangement over phosphotungstic acid/SiMCM-41 cyclohexanone oxime to ε-caprolactam - ScienceDirect
![Provide a detalied mechanism for the following Rxn [{Image src='currentproblem7510002552455744196.jpg' alt='' caption=''}] 1. NH2OH \rightarrow 2. H3O^{+} | Homework.Study.com Provide a detalied mechanism for the following Rxn [{Image src='currentproblem7510002552455744196.jpg' alt='' caption=''}] 1. NH2OH \rightarrow 2. H3O^{+} | Homework.Study.com](https://homework.study.com/cimages/multimages/16/screen_shot_2019-11-10_at_7.56.28_pm5381447725266143897.png)
Provide a detalied mechanism for the following Rxn [{Image src='currentproblem7510002552455744196.jpg' alt='' caption=''}] 1. NH2OH \rightarrow 2. H3O^{+} | Homework.Study.com
![PDF] A DFT study on secondary reaction pathways in the acid-catalysed Beckmann rearrangement of cyclohexanone oxime in aprotic solvent☆ | Semantic Scholar PDF] A DFT study on secondary reaction pathways in the acid-catalysed Beckmann rearrangement of cyclohexanone oxime in aprotic solvent☆ | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/55d436b7cfa7a77d65878c0691e12cbd4fc73af2/2-Figure1-1.png)
PDF] A DFT study on secondary reaction pathways in the acid-catalysed Beckmann rearrangement of cyclohexanone oxime in aprotic solvent☆ | Semantic Scholar
![SOLVED: Cyclohexanone reacts with hydroxylamine hydrochloride (NHzOHHCIJto give the oxime product, which reacts with sulfuric acid to give the 7-membered lactam (called caprolactam) as shown in the scheme below. Draw mechanisms for SOLVED: Cyclohexanone reacts with hydroxylamine hydrochloride (NHzOHHCIJto give the oxime product, which reacts with sulfuric acid to give the 7-membered lactam (called caprolactam) as shown in the scheme below. Draw mechanisms for](https://cdn.numerade.com/ask_images/0dabede8f2644037a0c15b2ea0746d41.jpg)
SOLVED: Cyclohexanone reacts with hydroxylamine hydrochloride (NHzOHHCIJto give the oxime product, which reacts with sulfuric acid to give the 7-membered lactam (called caprolactam) as shown in the scheme below. Draw mechanisms for
![A new procedure to obtain ε-caprolactam catalyzed by a guanidinium salt - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C7NJ03443A A new procedure to obtain ε-caprolactam catalyzed by a guanidinium salt - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C7NJ03443A](https://pubs.rsc.org/image/article/2017/NJ/c7nj03443a/c7nj03443a-s2_hi-res.gif)
A new procedure to obtain ε-caprolactam catalyzed by a guanidinium salt - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C7NJ03443A
![A Simplified Overall Kinetic Model for Cyclohexanone Oximation by Hydroxylamine Salt | Industrial & Engineering Chemistry Research A Simplified Overall Kinetic Model for Cyclohexanone Oximation by Hydroxylamine Salt | Industrial & Engineering Chemistry Research](https://pubs.acs.org/cms/10.1021/acs.iecr.6b00813/asset/images/medium/ie-2016-00813x_0009.gif)