enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. 3-Bromopentane - Wikipedia

    en.wikipedia.org/wiki/3-Bromopentane

    3-Bromopentane is a bromoalkane and isomer of bromopentane. It is a colorless liquid. References This page was last edited on 27 February 2024, at 20:34 (UTC). Text ...

  3. Bromopentane - Wikipedia

    en.wikipedia.org/wiki/Bromopentane

    Bromopentanes are a group of bromoalkanes consisting of pentane isomers with one or more hydrogen atoms replaced by bromine atoms. 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.

  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. 2-Bromopentane - Wikipedia

    en.wikipedia.org/wiki/2-Bromopentane

    2-Bromopentane is a bromoalkane and isomer of bromopentane. It is a colorless liquid. 2-Bromopentane is chiral and thus can be obtained as either of two stereoisomers designated as ( R )-2-bromopentane and ( S )-2-bromopentane, or as a racemic 1:1 mixture of the two enantiomers .

  6. Transfer hydrogenation - Wikipedia

    en.wikipedia.org/wiki/Transfer_hydrogenation

    It uses hydrogen donor compounds such as formic acid, isopropanol or dihydroanthracene, dehydrogenating them to CO 2, acetone, or anthracene respectively. [1] Often, the donor molecules also function as solvents for the reaction. A large scale application of transfer hydrogenation is coal liquefaction using "donor solvents" such as tetralin. [2 ...

  7. Organoboron chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoboron_chemistry

    The key property of organoboranes (R 3 B) and borates (R 4 B −, generated via addition of R − to R 3 B) is their susceptibility to reorganization. These compounds possess boron–carbon bonds polarized toward carbon. The boron-attached carbon is nucleophilic; [31] in borates, the nucleophicity suffices for intermolecular transfer to an ...

  8. Wall Street banks exit climate alliance as Trump 2.0 nears - AOL

    www.aol.com/finance/wall-street-banks-exit...

    Some of the biggest lenders in the US are beating a retreat from a UN-backed bank climate group in the final weeks before a new Trump administration prepares to take office.

  9. Enantioselective reduction of ketones - Wikipedia

    en.wikipedia.org/wiki/Enantioselective_reduction...

    Simple aryl ketones are reduced enantioselectively when a chiral amino alcohol ligand is employed. [4] (9) Transition metal catalysts have also been used with hydrogen gas as the stoichiometric reductant. Ketones with a chelating group undergo enantioselective reduction in the presence of a chiral Ru(BINAP) catalyst. [15]