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Dinitrobenzene

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Formula
  
C6H4N2O4

Dinitrobenzene Synthesis of mDINITROBENZENE PrepChemcom

Dinitrobenzenes are chemical compounds composed of a benzene ring and two nitro group (-NO2) substituents. The three possible arrangements of the nitro groups afford three isomers, 1,2-dinitrobenzene, 1,3-dinitrobenzene, and 1,4-dinitrobenzene. Each isomer has the chemical formula C6H4N2O4 and a molar mass of about 168.11 g/mol. 1,3-Dinitrobenzene is the most common isomer and it is used in the manufacture of explosives.

Contents

Dinitrobenzene Synthesis of mDINITROBENZENE PrepChemcom

Properties

Dinitrobenzene wwwsigmaaldrichcomcontentdamsigmaaldrichstr

The dinitrobenzenes are all crystalline solids. The boiling points of the three isomers are relatively close; however, the melting points significantly differ. 1,4-Dinitrobenzene, which has the highest symmetry, has the highest melting point.

Preparation

Dinitrobenzene Dinitrobenzene Wikipedia

1,3-Dinitrobenzene is accessible by nitration of nitrobenzene. The reaction proceeds under acid catalysis using sulfuric acid. The directing effect of the nitro group of nitrobenzene leads to 93% of the product resulting from nitration at the meta-position. The ortho- and para-products occur in only 6% and 1%, respectively.

Reactions

Dinitrobenzene 3dinitrobenzene C6H4N2O4 ChemSpider

Reduction of 1,3-dinitrobenzene with sodium sulfide in aqueous solution leads to 3-nitroaniline. Further reduction with iron and hydrochloric acid (HCl) gives m-phenylenediamine.

Dinitrobenzene 14Dinitrobenzene CAS Number 100254

References

Dinitrobenzene Wikipedia