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No, it is impossible and useless, besides both chloro-methylbenzene (phenylchloride, as intermediate product) and chlorobenzene (final) are also carcinogenic

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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.


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.


Is chlorobenzene the same as monochlorobenzene?

Yes, chlorobenzene and monochlorobenzene refer to the same chemical compound, which is a benzene ring with one chlorine atom attached.


What will happen if you add Sodium Benzoate to chlorinated water?

Benzene


How can a synthesis be devised to convert benzene into 1-bromo-3-chlorobenzene?

To convert benzene into 1-bromo-3-chlorobenzene, a synthesis can be devised by first reacting benzene with bromine to form bromobenzene. Then, bromobenzene can be further reacted with chlorine to substitute one bromine atom with a chlorine atom, resulting in 1-bromo-3-chlorobenzene. This process involves multiple steps and careful control of reaction conditions to achieve the desired product.


Is chlorobenzene polar or non polar?

Biphenyl has equal charges on both benzene rings, this material is non polar


What product is formed by the nitration of chlorobenzene?

p-nitrochlorobenzene and o-nitrochlorobenzene with negligible m-nitrochlorobenzene


How will you synthesis of phenol in small scale'?

There are many known syntheses of phenol. However, a few simple ones are: 1) hydrolysis of chlorobenzene: - chlorobenzene + water --> phenol + hydrochloric acid 2) oxidation of toluene: - toluene + oxygen --> phenol + carbon dioxide + water 3) oxidation of benzene with nitrous oxide: - benzene + nitrous oxide --> phenol + nitrogen


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.


Why Chlorobenzene is orthoparadirecting?

Chlorobenzene is ortho-para directing because the lone pairs on the chlorine atom can donate electron density through resonance, stabilizing the σ-complex formed during electrophilic aromatic substitution. This leads to preferential attack at the ortho and para positions of the benzene ring.


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.