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  2. TNT - Wikipedia

    en.wikipedia.org/wiki/TNT

    Trinitrotoluene (/ ˌ t r aɪ ˌ n aɪ t r oʊ ˈ t ɒ lj u iː n /), [5] [6] more commonly known as TNT (and more specifically 2,4,6-trinitrotoluene, and by its preferred IUPAC name 2-methyl-1,3,5-trinitrobenzene), [1] is a chemical compound with the formula C 6 H 2 (NO 2) 3 CH 3. TNT is occasionally used as a reagent in chemical synthesis ...

  3. Ammonal - Wikipedia

    en.wikipedia.org/wiki/Ammonal

    TNT is added to create T-ammonal which improves properties such as brisance. The mixture is often referred to as Tannerite, which is a brand of ammonal. The ammonium nitrate functions as an oxidizer and the aluminium as fuel. The use of the relatively cheap ammonium nitrate and aluminium makes it a replacement for pure TNT.

  4. Hexanitrostilbene - Wikipedia

    en.wikipedia.org/wiki/Hexanitrostilbene

    Hexanitrostilbene (HNS), also called JD-X, is an organic compound with the formula [(O 2 N) 3 C 6 H 2 CH] 2. It is a yellow-orange solid. [1] It is used as a heat-resistant high explosive. It is slightly soluble (0.1 - 5 g/100 mL) in butyrolactone, DMF, DMSO, and N-methylpyrrolidone.

  5. Balance equation - Wikipedia

    en.wikipedia.org/wiki/Balance_equation

    Often, constructing local balance equations is equivalent to removing the outer summations in the global balance equations for certain terms. [ 1 ] During the 1980s it was thought local balance was a requirement for a product-form equilibrium distribution , [ 10 ] [ 11 ] but Gelenbe 's G-network model showed this not to be the case.

  6. 2,4-Dinitrotoluene - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrotoluene

    Six positional isomers are possible for dinitrotoluene. The most common one is 2,4-dinitrotoluene. The nitration of toluene gives sequentially mononitrotoluene, DNT, and finally TNT. 2,4-DNT is the principal product from dinitration, the other main product being about 30% 1,3-DN2-T.

  7. 2,4,6-Trinitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/2,4,6-Trinitrobenzoic_acid

    2,4,6-Trinitrobenzoic acid is prepared by oxidation of 2,4,6-trinitrotoluene (TNT). It is formed by oxidation of TNT and nitric acid with chlorate [2] and with dichromate. [3] Upon heating, 2,4,6-trinitrobenzoic acid undergoes decarboxylation to give 1,3,5-trinitrobenzene. [4]

  8. Dunnite - Wikipedia

    en.wikipedia.org/wiki/Dunnite

    Dunnite can be used as a precursor to the highly stable explosive TATB (1,3,5-triamino-2,4,6-trinitrobenzene), by first dehydrating it to form picramide (attaching the ammonia as an amine group instead of an ion) and then further aminating it, using 1,1,1-trimethylhydrazinium iodide (TMHI) made from unsymmetrical dimethylhydrazine rocket fuel ...

  9. Octanitrocubane - Wikipedia

    en.wikipedia.org/wiki/Octanitrocubane

    Octanitrocubane (molecular formula: C 8 (NO 2) 8) is a proposed high explosive that, like TNT, is shock-insensitive (not readily detonated by shock). [1] The octanitrocubane molecule has the same chemical structure as cubane (C 8 H 8) except that each of the eight hydrogen atoms is replaced by a nitro group (NO 2).

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