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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
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.
1-Chlor-2-methylpropan; Usage on el.wikipedia.org Μεθυλο-1-χλωροπροπάνιο; Usage on eo.wikipedia.org Izobutila klorido; Usage on es.wikipedia.org 1-cloro-2-metilpropano; Usage on nl.wikipedia.org 1-chloor-2-methylpropaan; Usage on ru.wikipedia.org Изобутилхлорид; Usage on sh.wikipedia.org Izobutil hlorid
Pentane is an organic compound with the formula C 5 H 12 —that is, an alkane with five carbon atoms. The term may refer to any of three structural isomers, or to a mixture of them: in the IUPAC nomenclature, however, pentane means exclusively the n-pentane isomer, in which case pentanes refers to a mixture of them; the other two are called isopentane (methylbutane) and neopentane ...
Neopentane, or 2,2-dimethylpropane Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .
877 mg mL −1: Melting point: −131 °C (−204 °F; 142 K) Boiling point: ... Isobutyl chloride (1-chloro-2-methylpropane) is an organochlorine compound.
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 ...
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 + 1 ⁄ 2 O 2 → ClCH 2 CH 2 Cl + H 2 O. Secondary and tertiary alcohols react with hydrogen chloride to give the corresponding chlorides.