sodium borohydride and ethanol
This is an oxidation reaction cyclohexanol with acidified dichromate produces cyclohexanone
Cyclohexane can be oxidized into cyclohexanone by using an oxidizing agent such as potassium permanganate (KMnO4) or sodium dichromate (Na2Cr2O7) in the presence of a catalyst like sulfuric acid (H2SO4). The cyclohexane reacts with the oxidizing agent, resulting in the formation of cyclohexanol, which is further oxidized to cyclohexanone.
No, cyclohexanol is not an aromatic compound since it does not exhibit aromatic resonance stabilization (like benzene). Refer to Hückel's rule for clarification of the definition of an aromatic compound.
Cyclohexanone can be oxidized to adipic acid.
Cyclohexanol hasn't a polar molecule.
This is an oxidation reaction cyclohexanol with acidified dichromate produces cyclohexanone
cyclohexanone
Cyclohexane can be oxidized into cyclohexanone by using an oxidizing agent such as potassium permanganate (KMnO4) or sodium dichromate (Na2Cr2O7) in the presence of a catalyst like sulfuric acid (H2SO4). The cyclohexane reacts with the oxidizing agent, resulting in the formation of cyclohexanol, which is further oxidized to cyclohexanone.
Look at their functional groups u noob...learn chemistry..i have mr ropartz as my teacher...
No, cyclohexanol is not an aromatic compound since it does not exhibit aromatic resonance stabilization (like benzene). Refer to Hückel's rule for clarification of the definition of an aromatic compound.
The chemical formula for cyclohexanone is C6H10O
Cyclohexanone can be oxidized to adipic acid.
Cyclohexanol hasn't a polar molecule.
The Lucas test is applicable for cyclohexanol. Cyclohexanol is a secondary alcohol and s reported to react with the Lucas reagent after a few minutes.
Compared to phenol, cyclohexanol does not have double bonds. Therefore it is not a resonance stabilised anion and is neutral
its is neutral
Yes