Depends on the manufacturer. With that info, you can find the percentage of active.
Naphthalene (C10H8) is most soluble in non-polar solvents such as benzene, toluene, and carbon disulfide due to its non-polar nature and aromatic structure. These solvents can efficiently dissolve naphthalene molecules due to their similar non-polar characteristics.
The chemical compound used in mothballs is typically either naphthalene (C10H8) or paradichlorobenzene (C6H4Cl2). Both substances work by releasing vapors that deter insects from coming near clothes or fabric.
The equation C10H8 + 12 O2 → 10 CO2 + 4 H2O represents the complete combustion of naphthalene (C10H8), a polycyclic aromatic hydrocarbon. During combustion, naphthalene reacts with oxygen (O2) to produce carbon dioxide (CO2) and water (H2O), indicating it releases energy in the form of heat and light. This reaction is important in understanding the energy content of fuels and their environmental impact.
From the Wikipedia article on mothballs, "Older mothballs consisted primarily of naphthalene, but due to naphthalene's flammability, modern mothballs instead use 1,4-dichlorobenzene (also called para-dichlorobenzene, p-dichlorobenzene, or PDB)."
Carbon dioxide (CO2), iodine (I2), "moth balls," which are mostly naphthalene (C10H8), and arsenic (As) at really high temperatures.
C10h8
Naphthalene (C10H8) is most soluble in non-polar solvents such as benzene, toluene, and carbon disulfide due to its non-polar nature and aromatic structure. These solvents can efficiently dissolve naphthalene molecules due to their similar non-polar characteristics.
The molecular formula for naphthalene is C10H8. Naphthalene is a polycyclic aromatic hydrocarbon compound in which two benzene rings are fused together to form the structure of this compound.
naphathalene(solid)->naphathalene(liquid)
Pentane would be a good solvent at room temperature for naphthalene (C10H8) as it is non-polar and can dissolve non-polar compounds like naphthalene effectively. Water and ethanol are polar solvents and would not dissolve naphthalene well.
napthalene has got double ring system having alternate doublebond
Naphthalene would be most soluble in non-polar solvents such as benzene or hexane because it is a non-polar molecule. Polar solvents like water would not dissolve naphthalene well due to the lack of strong intermolecular interactions between the polar water molecules and the non-polar naphthalene molecules.
Naphthalene is not an element. Naphthalene is a combination of elements. Its formula is C10H8 and it is a compound, not an element.
The chemical compound used in mothballs is typically either naphthalene (C10H8) or paradichlorobenzene (C6H4Cl2). Both substances work by releasing vapors that deter insects from coming near clothes or fabric.
The equation C10H8 + 12 O2 → 10 CO2 + 4 H2O represents the complete combustion of naphthalene (C10H8), a polycyclic aromatic hydrocarbon. During combustion, naphthalene reacts with oxygen (O2) to produce carbon dioxide (CO2) and water (H2O), indicating it releases energy in the form of heat and light. This reaction is important in understanding the energy content of fuels and their environmental impact.
From the Wikipedia article on mothballs, "Older mothballs consisted primarily of naphthalene, but due to naphthalene's flammability, modern mothballs instead use 1,4-dichlorobenzene (also called para-dichlorobenzene, p-dichlorobenzene, or PDB)."
Carbon dioxide (CO2), iodine (I2), "moth balls," which are mostly naphthalene (C10H8), and arsenic (As) at really high temperatures.