Cyclohexene is very miscible with other organic solvents.
Toluene is soluble in ligroin. Both are hydrocarbons and have similar chemical properties, allowing them to mix and form a solution.
Yes, heptane is soluble in ligroin as both are non-polar solvents. They have similar chemical properties that allow them to dissolve in each other.
yes it does with heat, although it might take a super long time when heat up.
Because they are polar compound
Cyclohexene reacts with bromine water to give 1,2-dibromocyclohexane. The reaction between cyclohexene and potassium permanganate results in the oxidation of cyclohexene to form adipic acid.
Toluene is soluble in ligroin. Both are hydrocarbons and have similar chemical properties, allowing them to mix and form a solution.
No, cyclohexene is not soluble in water. Cyclohexene is a nonpolar compound, while water is a polar solvent. Generally, nonpolar compounds are not soluble in polar solvents like water. Therefore, cyclohexene tends to be immiscible or insoluble in water.
Yes, heptane is soluble in ligroin as both are non-polar solvents. They have similar chemical properties that allow them to dissolve in each other.
yes it does with heat, although it might take a super long time when heat up.
Cyclohexene will float on water due to its lower density compared to water. Its molecular structure is nonpolar and less dense, causing it to be less soluble in water and float on the surface.
There is a saying that all sodium salts are soluble in water.Furthermore, toluene and ligroin (a synonym for a fraction of petroleum ether) are both non-polar solvents that generally do not solvate ionic compounds. Water, on the other hand, has a large dipole moment and therefore is much more able to form strong intermolecular interactions with sodium and naphthionate ions in solution.
Because they are polar compound
Cyclohexene and cyclohexane are both insoluble in water and bases. Cyclohexene is insoluble in weak acids and soluble in strong acids and is thus considered a neutral compound. Cyclohexane is insoluble in everything, and is considered an inert compound.
Cyclohexene reacts with bromine water to give 1,2-dibromocyclohexane. The reaction between cyclohexene and potassium permanganate results in the oxidation of cyclohexene to form adipic acid.
The density of cyclohexene is approximately 0.811 g/ml. Therefore, 2 ml of cyclohexene would weigh approximately 1.622 grams.
Washing the crude cyclohexene with aqueous sodium carbonate helps neutralize any acidic impurities present in the crude product. This step can also help remove water-soluble impurities, resulting in a cleaner final product.
Cyclohexene + 4 H2O2 --> (in presence of NaWO3 * 2H2O and Phase Transfer Catalyst) yeilds adipic acid and 4H2O