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  2. 2-Chlorobutane - Wikipedia

    en.wikipedia.org/wiki/2-Chlorobutane

    This is because 2-chlorobutane possesses two different sets of β-hydrogens at the first and third carbons respectively, resulting in 1-butene or 2-butene. It is important to note that as a secondary alkyl halide, both E2 and Sn2 reactions are equally likely when reacting with a substance that can act as both a base and a nucleophile.

  3. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    An example is the pair propanal H 3 C–CH 2 –C(=O)-H and acetone H 3 C–C(=O)–CH 3: the first has a –C(=O)H functional group, which makes it an aldehyde, whereas the second has a C–C(=O)–C group, that makes it a ketone. Another example is the pair ethanol H 3 C–CH 2 –OH (an alcohol) and dimethyl ether H 3 C–O–CH 2 H (an ether).

  4. Topicity - Wikipedia

    en.wikipedia.org/wiki/Topicity

    Enantiotopic groups are identical and indistinguishable except in chiral environments. For instance, the CH 2 hydrogens in ethanol (CH 3 CH 2 OH) are normally enantiotopic, but can be made different (diastereotopic) if combined with a chiral center, for instance by conversion to an ester of a chiral carboxylic acid such as lactic acid, or if coordinated to a chiral metal center, or if ...

  5. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    The proper name for this molecule is either trans-2-fluoro-3-methylpent-2-ene because the alkyl groups that form the backbone chain (i.e., methyl and ethyl) reside across the double bond from each other, or (Z)-2-fluoro-3-methylpent-2-ene because the highest-priority groups on each side of the double bond are on the same side of the double bond ...

  6. Isomorphism (crystallography) - Wikipedia

    en.wikipedia.org/wiki/Isomorphism_(crystallography)

    Forsterite. In chemistry, isomorphism has meanings both at the level of crystallography and at a molecular level. In crystallography, crystals are isomorphous if they have identical symmetry and if the atomic positions can be described with a set of parameters (unit cell dimensions and fractional coordinates) whose numerical values differ only slightly.

  7. Eclipsed conformation - Wikipedia

    en.wikipedia.org/wiki/Eclipsed_conformation

    In chemistry an eclipsed conformation is a conformation in which two substituents X and Y on adjacent atoms A, B are in closest proximity, implying that the torsion angle X–A–B–Y is 0°. [1] Such a conformation can exist in any open chain, single chemical bond connecting two sp 3-hybridised atoms, and it is normally a conformational ...

  8. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    For octahedral complexes of formula MX 4 Y 2, two isomers also exist. (Here M is a metal atom, and X and Y are two different types of ligands.) In the cis isomer, the two Y ligands are adjacent to each other at 90°, as is true for the two chlorine atoms shown in green in cis-[Co(NH 3) 4 Cl 2] +, at left.

  9. 1,4-Dichlorobutane - Wikipedia

    en.wikipedia.org/wiki/1,4-Dichlorobutane

    1,4-Dichlorobutane is a chloroalkane with the molecular formula (CH 2 CH 2 Cl) 2. It is one of several structural isomers of dichlorobutane. They are all colorless liquids of low flammabiltity and of interest for specialized synthetic uses.