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  2. List of reagent testing color charts - Wikipedia

    en.wikipedia.org/wiki/List_of_reagent_testing...

    It is advised to check the references for photos of reaction results. [1] Reagent testers might show the colour of the desired substance while not showing a different colour for a more dangerous additive. [2] For this reason it is essential to use multiple different tests to show all adulterants.

  3. 1,2-Dibromoethylene - Wikipedia

    en.wikipedia.org/wiki/1,2-Dibromoethylene

    1,2-Dibromoethylene, also known as 1,2-dibromoethene and acetylene dibromide, is a dihalogenated unsaturated compound with one bromine on each of the two carbon atoms. There are two isomers of this compound, cis and trans .

  4. Borepin - Wikipedia

    en.wikipedia.org/wiki/Borepin

    They proceeded from 1,2-dibromocyclopentene and performed a van der Kerk method for boron heterocycle preparation. Next, they initiated a ring closure to form a 7-membered tin complex. Finally, they completed a tin-boron exchange reaction to afford the bicyclic borepin on the right.

  5. Kurnakov test - Wikipedia

    en.wikipedia.org/wiki/Kurnakov_test

    The Kurnakov test, also known as Kurnakov's reaction, is a chemical test that distinguishes pairs of cis- and trans-isomers of [PtA 2 X 2] (A = NH 3, X = halogen or pseudohalide). Upon treatment with thiourea , the trans -dihalides give less soluble white products, whereas the cis -dihalides give more soluble yellow products.

  6. trans-1,2-Diaminocyclohexane - Wikipedia

    en.wikipedia.org/wiki/Trans-1,2-Diaminocyclohexane

    trans-1,2-Diaminocyclohexane is an organic compound with the formula C 6 H 10 (NH 2) 2. This diamine is a building block for C 2-symmetric ligands that are useful in asymmetric catalysis. [1] A mixture of all three stereoisomers of 1,2-diaminocyclohexane is produced by the hydrogenation of o-phenylenediamine.

  7. Corey–Winter olefin synthesis - Wikipedia

    en.wikipedia.org/wiki/Corey–Winter_olefin...

    The Corey-Winter olefination is a stereospecific reaction: [1] a trans-diol gives a trans-alkene, while a cis-diol gives a cis-alkene as the product. For instance, cis- and trans-1,2-cyclodecanediol gives the respective cis- and trans-cyclodecene.

  8. 1,2-Dichloroethylene - Wikipedia

    en.wikipedia.org/wiki/1,2-dichloroethylene

    1,2-Dichloroethylene or 1,2-DCE is the name for a pair of organochlorine compounds with the molecular formula C 2 H 2 Cl 2. The two compounds are isomers, each being colorless liquids with a sweet odor. It can exist as either of two geometric isomers, cis-1,2-dichloroethene or trans-1,2-dichloroethene, but is often used as a mixture of the two ...

  9. Biuret test - Wikipedia

    en.wikipedia.org/wiki/Biuret_test

    Despite its name, the reagent does not in fact contain biuret [(H 2 N−CO−) 2 NH]. The test is named so because it also gives a positive reaction to the peptide-like bonds in the biuret molecule. In this assay, the copper(II) binds with nitrogen atoms present in the peptides of proteins. In a secondary reaction, the copper(II) is reduced to ...