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  2. Newman projection - Wikipedia

    en.wikipedia.org/wiki/Newman_projection

    3D structure A Newman projection is a drawing that helps visualize the 3-dimensional structure of a molecule. [ 1 ] This projection most commonly sights down a carbon-carbon bond, making it a very useful way to visualize the stereochemistry of alkanes.

  3. Neopentane - Wikipedia

    en.wikipedia.org/wiki/Neopentane

    The preferred IUPAC name is the systematic name 2,2-dimethylpropane, but the substituent numbers are superfluous because it is the only possible “dimethylpropane”. A neopentyl group attached to a generic group R. A neopentyl substituent, often symbolized by "Np", has the structure Me 3 C–CH 2 – for instance neopentyl alcohol (Me 3 CCH 2 OH

  4. File:1-Chlor-2-methyl propane-Structural Formula V.1.svg

    en.wikipedia.org/wiki/File:1-Chlor-2-methyl...

    The following other wikis use this file: Usage on de.wikipedia.org Chlorbutane; 1-Chlor-2-methylpropan; Usage on el.wikipedia.org Μεθυλο-1-χλωροπροπάνιο

  5. Isobutyl chloride - Wikipedia

    en.wikipedia.org/wiki/Isobutyl_chloride

    Isobutyl chloride (1-chloro-2-methylpropane) is an organochlorine compound. It is a chlorinated derivative of isobutane. Synthesis

  6. Bromopentane - Wikipedia

    en.wikipedia.org/wiki/Bromopentane

    They have the formula C 5 H 12–n Br n, where n = 1–12 is the number of bromine atoms. They are colorless liquids. ... 1-bromo-2,2-dimethylpropane, also known as ...

  7. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    The secondary functional groups are: a hydroxy- at carbon 5, a chloro- at carbon 11, a methoxy- at carbon 15, and a bromo- at carbon 18. Grouped with the side chains, this gives 18-bromo-12-butyl-11-chloro-4,8-diethyl-5-hydroxy-15-methoxy. There are two double bonds: one between carbons 6 and 7, and one between carbons 13 and 14.

  8. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    H 2 C=CH 2 + HCl → CH 3 CH 2 Cl. In oxychlorination, hydrogen chloride instead of the more expensive chlorine is used for the same purpose: CH 2 =CH 2 + 2 HCl + 12 O 2 → ClCH 2 CH 2 Cl + H 2 O. Secondary and tertiary alcohols react with hydrogen chloride to give the corresponding chlorides.

  9. File:2,2-dimethylpropane-1,3-diol 200.svg - Wikipedia

    en.wikipedia.org/wiki/File:2,2-dimethylpropane-1...

    The following other wikis use this file: Usage on azb.wikipedia.org نئوپنتیل قلوسویل; Usage on de.wikipedia.org Neopentylglycol; Usage on es.wikipedia.org