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  2. Cyclohexanone oxime - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanone_oxime

    Cyclohexanone oxime can be prepared from the condensation reaction between cyclohexanone and hydroxylamine: [1] C 5 H 10 CO + H 2 NOH → C 5 H 10 C=NOH + H 2 O. Alternatively, another industrial route involves the reaction of cyclohexane with nitrosyl chloride, which is a free-radical reaction. This method is advantageous as cyclohexane is ...

  3. Cyclohexanone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanone

    Cyclohexanone is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [11]. C 6 H 12 + O 2 → (CH 2) 5 CO + H 2 O. This process forms cyclohexanol as a by-product, and this mixture, called "KA Oil" for ketone-alcohol oil, is the main feedstock for the production of adipic acid.

  4. Oxime - Wikipedia

    en.wikipedia.org/wiki/Oxime

    In organic chemistry, an oxime is an organic compound belonging to the imines, with the general formula RR’C=N−OH, where R is an organic side-chain and R' may be hydrogen, forming an aldoxime, or another organic group, forming a ketoxime. O-substituted oximes form a closely related family of compounds.

  5. C6H11NO - Wikipedia

    en.wikipedia.org/wiki/C6H11NO

    The molecular formula C 6 H 11 NO may refer to: Caprolactam (CPL) Cyclohexanone oxime; N-Formylpiperidine; Nylon 6 (repeating unit), or polycaprolactam

  6. Isobutyric anhydride - Wikipedia

    en.wikipedia.org/wiki/Isobutyric_anhydride

    Isobutyric anhydride is used as an acylating agent in organic synthesis. Its primary application is in the production of esters, such as cyclohexanone oxime. [5] Isobutyric anhydride is used in the synthesis of various dyes. [6] It is also used in the production of cellulose derivatives, such as cellulose isobutyrate and cellulose acetate ...

  7. Cyclohexenone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexenone

    Cyclohexenone is a widely used building block in organic synthesis chemistry, as it offers many different ways to extend molecular frameworks. As an enone , cyclohexenone is easily adapted to Michael addition with nucleophiles (such as enolates or silyl enol ethers) or, it could be employed by a Diels-Alder reaction with electron-rich dienes .

  8. 10 Christmas bedding essentials for a cozy guest room - AOL

    www.aol.com/lifestyle/christmas-bedding...

    Create a cozy bedroom even Mrs. Claus would envy with Christmas quilts, flannel sheets, plaid throw blankets and festive throw pillows.

  9. Cyclohexanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanol

    Cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [5]. 2 C 6 H 12 + O 2 → 2 C 6 H 11 OH. This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid.