Nitrogen is this element's chemical name. Its symbol on the Periodic Table is N. It is a colourless gas with the atomic number 7.
Hi ,As you know from the structures of both the compounds that toluene has a methyl group on the benzene ring which is electron releasing group and hence activate the benzene ring by pushing the elctrons on the benzene ring. On the other hand nitro group on the benzene ring is electron withdrawing group which deactivates the benzene ring by withdrawing the electrons from the benzene ring . Now in the nitration attack of the nucleophile ( NO2 +) takes place. Hence reaction will takes place on that benzene faster which have more electron density on its ring which is the case of toluene.
O-Nitrotoluene can be prepared from benzene via a multistep reaction process. First, benzene is nitrated to form nitrobenzene using a mixture of nitric acid and sulfuric acid. Next, nitrobenzene is methylated to form o-nitrotoluene by reacting it with methyl iodide in the presence of a base like sodium hydroxide. The final product is then separated and purified using appropriate techniques.
Thermocol is another name for polystyrene (PS), which is a type of plastic. Benzene is an industrial solvent, and it's primary use is to make styrene. The chemical structure of benzene, a non-polar organic hydrocarbon solvent, and of PS is such that benzene will dissolve styrene and polystyrene.
Fractional distillation is commonly used to separate benzene from a mixture of benzene and methyl benzene. Benzene has a lower boiling point compared to methyl benzene, allowing it to be separated by distillation based on the difference in their boiling points.
Benzene is a colorless, aromatic hydrocarbon with a ring structure, while nitrobenzene is a derivative of benzene with a nitro group (-NO2) attached to the ring. Nitrobenzene is a pale yellow liquid with a distinctive odor, and it is often used as a precursor in the synthesis of various chemicals.
With hydrogen in a catalized reaction
The IUPAC name for butyl benzene is 4-phenylbutane. The IUPAC name for phenyl butane is 1-phenylbutane.
Benzaldehyde has the formula C7H6O, it has the carbonyl carbon of the aldehyde bound to a benzene ring. You can't have a =O unit bound directly to the benzene ring because you would have a carbon with five bonds.
Nitration of nitrobenzene is more difficult because the nitro group is an electron-withdrawing group, making the nitrobenzene less reactive towards electrophilic aromatic substitution reactions. In contrast, benzene is more reactive because it does not have any electron-withdrawing groups attached to it.
The chemical formula for trichloronitrobenzene is C6H2Cl3NO2.
No. Up to now it is not registered in CIB.
The common name of acetophenone is phenyl methyl ketone.
1. benzene to nitro benzene through nitration 2. nitro benzene to m-bromonitrobenzene by bromination 3. m-bromonitrobenzene to m-bromoaniline through halogenation in presence of Sn+HCl.
M-nitroaniline can be prepared from m-dinitrobenzene by reducing one of the nitro groups to an amino group. One common method is to use a reducing agent like tin and hydrochloric acid in a strongly acidic medium, which leads to the conversion of one nitro group to an amino group to yield m-nitroaniline.
Yes, nitrobenzene is a polar compound due to the electronegative nitro group attached to the benzene ring. This creates an uneven distribution of charge, with the nitro group being more negative and the benzene ring being more positive, resulting in a polar molecule.
The molecular name of benzene is C6H6.