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What is the chlorobenzene boiling point?
The chlorobenzene boiling point is 131 oC.
How easy is it to separate compounds of chlorobenzene and bromobenzene?
Separating compounds like chlorobenzene and bromobenzene can be challenging because they are structurally similar. One common method is fractional distillation, but this may not achieve complete separation. Another approach is chemical separation using specific reactions that selectively target one of the compounds.
How to prepare acetophenone from phenol in not more than 2 steps?
One way to prepare acetophenone from phenol in two steps is to first react phenol with carbon tetrachloride and aluminum chloride to form chlorobenzene, and then treat the chlorobenzene with copper cyanide to form acetophenone.
Which benzene is used in dry cleaning?
Perchloroethylene (Perc) is the benzene compound commonly used in dry cleaning. It is effective in removing dirt and stains from clothing without causing damage to the fabric.
At what temperature does benzene react with chlorine without catalyst?
Benzene reacts with chlorine at room temperature without the need for a catalyst. This reaction occurs through a substitution reaction where one or more hydrogen atoms in benzene are replaced by chlorine atoms to form chlorobenzene.
Is nitrogen present in chlorobenzene?
The chemical formula of chlorobenzene is C6H5Cl; chlorobenzene don't contain nitrogen.
What is the chlorobenzene boiling point?
The chlorobenzene boiling point is 131 oC.
What are the reactions of chlorobenzene?
Chlorobenzene can undergo various reactions, including substitution, nitration, and halogenation. It can also be converted to phenol through hydrolysis. Additionally, chlorobenzene can participate in electrophilic aromatic substitution reactions.
Why chlorobenzene is less reactive than Brazil chloride?
Chlorobenzene is less reactive than benzyl chloride because the chlorine atom in chlorobenzene is less polarizable than the bromine atom in benzyl chloride. As a result, the chlorine atom is less prone to nucleophilic attack, making chlorobenzene less reactive.
Is chlorobenzene a haloalkane?
No, chlorobenzene is not a haloalkane. It is a halobenzene, which is a type of aromatic compound where a halogen atom (in this case chlorine) is attached to a benzene ring.
To avoid carcinogenicity by the use of benzene to be chlorinated to become chlorobenzene could it be possible to convert far less toxic toluene to chlorobenzene?
Yes, toluene can be chlorinated to form chlorobenzene without the need to use benzene. This process can help avoid the carcinogenic risks associated with benzene exposure. Toluene is less toxic than benzene and can be a safer alternative for producing chlorobenzene.
How Chlorobenzene give white precipitate on reaction with acidified silver nitrate solution this is correct or not?
Yes, this statement is correct. When chlorobenzene reacts with acidified silver nitrate solution, a white precipitate of silver chloride is formed due to the displacement reaction between the chloride ion from chlorobenzene and the silver ion from silver nitrate.
Why dipole moment of chlorobenzene is lower than that of cyclohexyl chloride?
The dipole moment of chlorobenzene is lower than cyclohexyl chloride because benzene ring in chlorobenzene has resonance delocalization of electrons which reduces the polarity of the molecule, whereas in cyclohexyl chloride, the chlorine atom is directly attached to a saturated carbon atom leading to a more localized dipole moment.
In benzene and chlorobenzene which one is more polar?
Chlorobenzene is more polar than benzene because it has a chlorine atom attached to the benzene ring, which induces a dipole moment and increases its overall polarity compared to benzene.
What product is formed by the nitration of chlorobenzene?
p-nitrochlorobenzene and o-nitrochlorobenzene with negligible m-nitrochlorobenzene
How easy is it to separate compounds of chlorobenzene and bromobenzene?
Separating compounds like chlorobenzene and bromobenzene can be challenging because they are structurally similar. One common method is fractional distillation, but this may not achieve complete separation. Another approach is chemical separation using specific reactions that selectively target one of the compounds.
Where will be NO2 plus group attached in Nitration of chlorobenzene?
In the nitration of chlorobenzene, the NO2 group will typically replace one of the hydrogen atoms on the benzene ring, resulting in the formation of nitrochlorobenzene. The nitration reaction occurs at the ortho or para position to the chlorine atom due to the directing effect of the chlorine substituent.
