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  2. Nitration - Wikipedia

    en.wikipedia.org/wiki/Nitration

    In organic chemistry, nitration is a general class of chemical processes for the introduction of a nitro group (−NO2) into an organic compound. The term also is applied incorrectly to the different process of forming nitrate esters (−ONO2) between alcohols and nitric acid (as occurs in the synthesis of nitroglycerin).

  3. Barton reaction - Wikipedia

    en.wikipedia.org/wiki/Barton_reaction

    The Barton reaction, also known as the Barton nitrite ester reaction, is a photochemical reaction that involves the photolysis of an alkyl nitrite to form a δ- nitroso alcohol. Discovered in 1960, the reaction is named for its discoverer, Nobel laureate Sir Derek Barton. [1] Barton's Nobel Prize in Chemistry in 1969 was awarded for his work on ...

  4. Pentaerythritol tetranitrate - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol_tetranitrate

    Infobox references. Pentaerythritol tetranitrate (PETN), also known as PENT, pentyl, PENTA (ПЕНТА, primarily in Russian), TEN (tetraeritrit nitrate), corpent, or penthrite (or, rarely and primarily in German, as nitropenta), is an explosive material. It is the nitrate ester of pentaerythritol, and is structurally very similar to nitroglycerin.

  5. Nitro compound - Wikipedia

    en.wikipedia.org/wiki/Nitro_compound

    In organic chemistry, nitro compounds are organic compounds that contain one or more nitro functional groups (−NO2). The nitro group is one of the most common explosophores (functional group that makes a compound explosive) used globally. The nitro group is also strongly electron-withdrawing. Because of this property, C−H bonds alpha ...

  6. Reduction of nitro compounds - Wikipedia

    en.wikipedia.org/wiki/Reduction_of_nitro_compounds

    The reduction of nitro compounds are chemical reactions of wide interest in organic chemistry. The conversion can be effected by many reagents. The nitro group was one of the first functional groups to be reduced. Alkyl and aryl nitro compounds behave differently. Most useful is the reduction of aryl nitro compounds.

  7. Nitrate - Wikipedia

    en.wikipedia.org/wiki/Nitrate

    Nitrate is a polyatomic ion with the chemical formula NO−3. Salts containing this ion are called nitrates. Nitrates are common components of fertilizers and explosives. [ 1 ] Almost all inorganic nitrates are soluble in water. An example of an insoluble nitrate is bismuth oxynitrate.

  8. Nitrocellulose - Wikipedia

    en.wikipedia.org/wiki/Nitrocellulose

    Infobox references. Nitrocellulose (also known as cellulose nitrate, flash paper, flash cotton, guncotton, pyroxylin and flash string, depending on form) is a highly flammable compound formed by nitrating cellulose through exposure to a mixture of nitric acid and sulfuric acid. One of its first major uses was as guncotton, a replacement for ...

  9. Electrophilic aromatic substitution - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_aromatic...

    Electrophilic aromatic substitution (SEAr) is an organic reaction in which an atom that is attached to an aromatic system (usually hydrogen) is replaced by an electrophile. Some of the most important electrophilic aromatic substitutions are aromatic nitration, aromatic halogenation, aromatic sulfonation, alkylation Friedel–Crafts reaction and ...