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  2. Neopentane - Wikipedia

    en.wikipedia.org/wiki/Neopentane

    Therefore, neopentane is a gas at room temperature and atmospheric pressure, while the other two isomers are (barely) liquids. The melting point of neopentane (−16.6 °C), on the other hand, is 140 degrees higher than that of isopentane (−159.9 °C) and 110 degrees higher than that of n -pentane (−129.8 °C).

  3. Jmol - Wikipedia

    en.wikipedia.org/wiki/Jmol

    JSmol is an implementation in JavaScript of the functionality of Jmol. [4] It can hence be embedded in web pages to display interactive 3D models of molecules and other structures without the need for any software apart from the web browser (it does not use Java).

  4. Neopentyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_alcohol

    Neopentyl alcohol can be prepared from the hydroperoxide of diisobutylene. [3] It can also be prepared by the reduction of trimethylacetic acid with lithium aluminium hydride.

  5. 2,2-Dimethylbutane - Wikipedia

    en.wikipedia.org/wiki/2,2-Dimethylbutane

    Butlerov's student V. Goryainov originally discovered neohexane in 1872 by cross-coupling of zinc ethyl with tert-butyl iodide. [5]2,2-Dimethylbutane can be synthesised by the hydroisomerisation of 2,3-dimethylbutane using an acid catalyst.

  6. Isopentane - Wikipedia

    en.wikipedia.org/wiki/Isopentane

    It is one of three structural isomers with the molecular formula C 5 H 12, the others being pentane (n-pentane) and neopentane (2,2-dimethylpropane). Isopentane is commonly used in conjunction with liquid nitrogen to achieve a liquid bath temperature of −160 °C.

  7. 1,4-Dichlorobut-2-ene - Wikipedia

    en.wikipedia.org/wiki/1,4-Dichlorobut-2-ene

    Chloroprene is a monomer for the production of synthetic rubbers such as Neoprene.It is produced from butadiene in a three-step process. The first step is the liquid- or vapour-phase chlorination of butadiene to a mixture of 3,4-dichlorobut-1-ene and 1,4-dichlorobut-2-ene (both isomers).

  8. Neopentylamine - Wikipedia

    en.wikipedia.org/wiki/Neopentylamine

    Read; Edit; View history; General ... 3D model . Interactive image; ChemSpider: ... The molecule is the primary amine derivative of neopentane, (CH 3) ...

  9. Neophyl chloride - Wikipedia

    en.wikipedia.org/wiki/Neophyl_chloride

    Neophyl chloride can be used to form an organolithium reagent, neophyl lithium, by reaction with lithium.Organolithium reagents are useful due to their nucleophilic properties and their ability to form carbon-to-carbon bonds, like in reactions with carbonyls.

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