By solvent extraction with water.
By fractional distillation.
Fractional distillation in a distillation column will remove benzene from hexane. The vapor-liquid-equilibrium data indicate that depending on initial and desired concentrations, multiple theoretical stages will likely be needed. See also vapor liquid equilibrium chart for benzene and hexane.
No, it is an ionic compound which is soluble in water (a polar solvent) but not in Hexane ( a non polar solvent).
Sunlight wouldn't be enough energy to carry out the reaction between n-hexane and bromine. The energy source, however, may have been written has "hv" as a way to describe the radiation or high-wavelength energy for the reaction, which is possible in a more controlled environment. In this scenario, the reaction between n-hexane and bromine is a bromination reaction--generation of a bromine radical and attaching one or more bromine molecules to hexane. It is more likely that it will attach to a secondary carbon rather its primary, and its location of attachment between the available secondary carbons would be a mixture.
No, Magnesium Chloride is not soluble in Hexane. Magnesium Chloride is an ionic compound with strong ionic bonds, and hexane is a nonpolar solvent. Ionic compounds like Magnesium Chloride are typically insoluble in nonpolar solvents like hexane.
If this is supposed to be an alkene test, then no, hexane will not react with bromine water to take away its color as it is an alkane and therefore contains no double bonds. But bromine water will react with sodium hydroxide; bromine water contains either HCl or H2SO4, both of which will of course react with sodium hydroxide. In addition, I believe (from some experiments like this that I've done recently) that sodium hydroxide will actually react with the free bromine in the bromine water, as evidenced by the change in color from the orange-ish color of bromine water to a pale yellow.
Bromine (Br2) dissolves in cyclohexane due to its nonpolar nature, which is similar to cyclohexane's nonpolar composition. In contrast, bromine does not dissolve in water because water is a polar solvent and bromine is nonpolar, leading to poor solubility due to the mismatch in polarity.
Bromine is nonpolar and needs a nonpolar solvent to do the bromination reaction. CCl4 is a heavy, nonpolar solvent that dissolves the heavy Br2 molecule. With lighter nonpolar solvents such as hexane, the high density Bromine settles out.
Elemental bromine would be expected to be soluble in hexane. Bromine, Br2(l), is non-polar; hexane, C6H14(l) is also non-polar. Like dissolves like.
Fractional distillation in a distillation column will remove benzene from hexane. The vapor-liquid-equilibrium data indicate that depending on initial and desired concentrations, multiple theoretical stages will likely be needed. See also vapor liquid equilibrium chart for benzene and hexane.
The observation in the reaction of hexane with bromine water is that the color of bromine water changes from orange to colorless as the bromine is being added to the hexane. This indicates that a reaction between hexane and bromine is taking place, forming a colorless product.
Bromine is soluble in water.
One simple chemical test to distinguish between benzene and hexane is the Bromine test. Benzene will not react with bromine in the absence of a catalyst, while hexane will readily react with bromine to form a colorless product.
Bromine water will go clear in the dark, while hexane will not change color in either light or dark conditions.
No, it is an ionic compound which is soluble in water (a polar solvent) but not in Hexane ( a non polar solvent).
Terpenoids are large hydrocarbons. They are generally non polar and hydrophobic. Hexane is a non polar solvent. When solutes and solvents have compatible polarities ,the solute dissolves in the solvent. As terpenoids and hexane are non polar , terpenoids would dissolve in hexane.
After hexane solvent evaporates, any substances dissolved in the hexane will remain behind. This could be a residue or crystals of the solute that was dissolved in the hexane. It is important to handle any remaining material with proper precautions as it may be flammable or toxic.
Sunlight wouldn't be enough energy to carry out the reaction between n-hexane and bromine. The energy source, however, may have been written has "hv" as a way to describe the radiation or high-wavelength energy for the reaction, which is possible in a more controlled environment. In this scenario, the reaction between n-hexane and bromine is a bromination reaction--generation of a bromine radical and attaching one or more bromine molecules to hexane. It is more likely that it will attach to a secondary carbon rather its primary, and its location of attachment between the available secondary carbons would be a mixture.