No. You can oxidize cyclohexanol into clyclohexanone by using potassium dichromate solution under reflux.
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.
Cyclohexanone can be oxidized to adipic acid.
Cyclohexane (or cyclohexanone, if that is what you meant) is usually found as a pure substance, and is produced industrially as such. It consists of a single molecule. However, cyclohexane can be impure if it is tainted or something is added to it.
Cyclohexane is flammable.
Yes
This is an oxidation reaction cyclohexanol with acidified dichromate produces cyclohexanone
Cyclohexanone can be oxidized to adipic acid.
Cyclohexane (or cyclohexanone, if that is what you meant) is usually found as a pure substance, and is produced industrially as such. It consists of a single molecule. However, cyclohexane can be impure if it is tainted or something is added to it.
The chemical formula for cyclohexanone is C6H10O
Cyclohexane is flammable.
Yes
This is an oxidation reaction cyclohexanol with acidified dichromate produces cyclohexanone
No, sodium chloride is not soluble in cyclohexane.
Cyclohexane has no charge. It is a compound, not an ion.
Cyclohexane (C6H12) is a cycloalkane, not an esther.
No, cyclohexane is a neutral compound.
water is polar and the cyclohexane is not
cyclohexanone