What is the molar mass of naphthalene?

128.1705 g/molNaphthalene / Molar mass

What is the formula of naphthalene?

C10H8Naphthalene / Formula

How many moles are in naphthalene?

The molar mass of naphthalene is 128.17052 g/mol. Naphthalene’s chemical formula C10 H8 tells us that there are 10 carbon atoms and 8 hydrogen atoms….

What is the molar mass of naphthalene should be in 4 SF?

How is naphthalene Synthesised?

Hint: There are five steps involved in the formation of naphthalene by Haworth synthesis. These are Friedel craft acylation, Clemmenson’s reaction, heating the compound, Clemmenson reaction, and dehydrogenation. Two aromatic rings joined are known as naphthalene.

What is type of compound is naphthalene?

Naphthalene is an organic compound with formula C10H8. It is the simplest polycyclic aromatic hydrocarbon, and is a white crystalline solid with a characteristic odor that is detectable at concentrations as low as 0.08 ppm by mass.

What are the dangers of naphthalene?

Naphthalene has been shown to cause tissue damage and cancer in the nasal passages and lungs of rats and mice exposed to high levels in laboratory studies. It is considered a possible carcinogen for humans, although there is not yet sufficient evidence to prove it causes cancer in humans.

What is the theoretical melting point of naphthalene?

The melting point of naphthalene is approximately between 79 and 82 degrees Celsius. The physical state of this chemical is as a white solid that is insoluble in water. This chemical also has a boiling point between 217 and 218 degrees Celsius.

What is the molecular weight of naphthalene?

(2,5,6) EPA has classified naphthalene as a Group C, possible human carcinogen. The chemical formula for naphthalene is C10H8 , and its molecular weight is 128.19 g/mol. (1) Naphthalene occurs as a white solid or powderthat is insoluble in water. (0.084 parts per million, ppm).

Is naphthalene more reactive than benzene?

Answers : (1) The smallest such hydrocarbon is naphthalene. Naphthalene is more reactive than benzene, both in substitution and addition reactions, and these reactions tend to proceed in a manner that maintains one intact benzene ring.