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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. The nitration of 4-nitrotoluene gives 2,4-DNT. [5]
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2,5-Dinitrotoluene; 2,6-Dinitrotoluene; 3,4-Dinitrotoluene; 3,5-Dinitrotoluene External links. Media related to Dinitrotoluenes at Wikimedia Commons; This page was ...
The template synthesis method uses a nanoporous membrane template composed of cylindrical pores of uniform diameter to make fibrils (solid nanofiber) and tubules (hollow nanofiber). [ 51 ] [ 52 ] This method can be used to prepare fibrils and tubules of many types of materials, including metals, semiconductors and electronically conductive ...
2,4-Diaminotoluene is an aromatic organic compound with the formula C 6 H 3 (NH 2) 2 CH 3. It is one isomer of six with this formula. It is a white solid, although commercial samples are often yellow-tan.
18-Crown-6 can be synthesized by the Williamson ether synthesis using potassium ion as the template cation. Structure of nickel-aquo nitrate complex of the ligand derived from the templated trimerization of 2-aminobenzaldehyde. [5] The phosphorus analogue of an aza crown can be prepared by a template reaction. [6]
The Corey–Fuchs reaction, also known as the Ramirez–Corey–Fuchs reaction, is a series of chemical reactions designed to transform an aldehyde into an alkyne. The formation of the 1,1-dibromoolefins via phosphine-dibromomethylenes was originally discovered by Desai, McKelvie and Ramirez.