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m-dinitrobenzene is an environmentally friendly.
benzene,as it can undergo nitration to give nitrobenzene
because nitro group is ring deactivating group, nitration of nitro benzene is more difficult than benzene.
You think probable to nitration.
To form an active electrophile NO2+
m-dinitrobenzene is an environmentally friendly.
For example nitrobenzene is obtained by nitration of benzene.
benzene,as it can undergo nitration to give nitrobenzene
because nitro group is ring deactivating group, nitration of nitro benzene is more difficult than benzene.
Nitration: H2SO4 C6H6 + HONO2 ---------> C6H5NO2 + H2O Nitric Acid Nitrobenzene Nitration: H2SO4 C6H6 + HONO2 ---------> C6H5NO2 + H2O Nitric Acid Nitrobenzene Nitration: .................H2SO4 C6H6 + HONO2 ---------> C6H5NO2 + H2O .....Nitric Acid ......Nitrobenzene
Dinitroproducts are formed when the incorrect temperature range is used. You maintain a proper temperature range for the experiment to avoid such things.
Well a standard nitration with mixed acids at elevated temperatures. One could just follow the nitration of its brother, acetylsalicylicacid (ASA) as in the same way TriNitroPhenol (TNP) is made.
Nitrobenzene is created by nitration of benzene with a mixture of concentrated nitric acid, sulfuric acid, and water. Producing nitrobenzene is one of the most dangerous processes preformed in the chemical industry.
Howard William Post has written: 'The nitration of substituted anilines ..' -- subject(s): Aniline, Nitration 'The chemistry of the aliphatic orthoesters' -- subject(s): Esters
You think probable to nitration.
bhkih
It's a catalyst