Liquid naphthalene is typically obtained by melting solid naphthalene. This can be done by heating solid naphthalene to around 80 degrees Celsius until it liquefies. It is important to handle naphthalene with care as it is toxic and flammable.
The IUPAC name for naphthalene is "naphthalene".
The smell of naphthalene will likely be present in the mixture, although it may be less intense due to the dilution with chalk powder. The naphthalene odor may be detectable, especially in close proximity to the mixture.
To determine the number of naphthalene molecules in a 1-gram naphthalene mothball, you would first calculate the number of moles of naphthalene using its molar mass (C10H8) and then use Avogadro's number to convert moles to molecules. Given that naphthalene's molar mass is 128.17 g/mol, you would find that there are approximately 6.022 x 10^21 molecules in a 1-gram naphthalene mothball.
Yes, naphthalene is sparingly soluble in cyclohexane. Naphthalene is a nonpolar compound, like cyclohexane, so they can dissolve in each other to a limited extent.
Liquid naphthalene is typically obtained by melting solid naphthalene. This can be done by heating solid naphthalene to around 80 degrees Celsius until it liquefies. It is important to handle naphthalene with care as it is toxic and flammable.
In this context, the solute is naphthalene while the solvent is air. Naphthalene is the substance that is being dissolved in the air.
Naphthalene can be separated from common salt by sublimation since naphthalene sublimes at a lower temperature than common salt. By heating the mixture, naphthalene will turn directly from a solid to a gas, leaving behind the common salt as a solid residue. The naphthalene gas can then be cooled and collected back as a solid.
Yes, naphthalene is soluble in chloroform. When added to chloroform, naphthalene dissolves because they have similar solubility characteristics.
Naphthalene is not very soluble in water, meaning it does not dissolve easily in water. The solubility of naphthalene in water is very low.
Naphthalene can be separated from sodium chloride by sublimation. When the mixture is heated, naphthalene will sublimate, turning from a solid to a gas, and can be collected separately from the solid sodium chloride.
At standard temperature and pressure, naphthalene is a white crystalline solid.
Potassium iodide is not typically found in naphthalene. Naphthalene is a hydrocarbon compound and does not naturally contain potassium iodide.
When sulfur is added to naphthalene, it can form a chemical compound known as sulfurized naphthalene. This can improve the lubricity and anti-wear properties of the naphthalene, making it suitable for use as a lubricant or as an additive in lubricating oils.
The IUPAC name for naphthalene is "naphthalene".
The smell of naphthalene will likely be present in the mixture, although it may be less intense due to the dilution with chalk powder. The naphthalene odor may be detectable, especially in close proximity to the mixture.
Paradichlorobenzene dissolves in naphthalene because they are both nonpolar compounds. Nonpolar substances are soluble in nonpolar solvents like naphthalene due to similar attractive forces between molecules, known as London dispersion forces. This allows paradichlorobenzene to mix and dissolve evenly in naphthalene.