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  2. Cyclopentanecarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Cyclopentanecarboxylic_acid

    It is a colorless nonvolatile oil. It can be produced by the palladium-catalyzed hydrocarboxylation of cyclopentene: [2] C 5 H 8 + CO + H 2 O → C 5 H 9 CO 2 H. An alternative route involves base-induced ring contraction of 2-chlorocyclohexanone to give the ester methyl cyclopentanecarboxylate, which can be hydrolyzed to the carboxylic acid. [3]

  3. Koch reaction - Wikipedia

    en.wikipedia.org/wiki/Koch_reaction

    The Koch reaction is an organic reaction for the synthesis of tertiary carboxylic acids from alcohols or alkenes and carbon monoxide.Some commonly industrially produced Koch acids include pivalic acid, 2,2-dimethylbutyric acid and 2,2-dimethylpentanoic acid. [1]

  4. 2-Ethylhexanol - Wikipedia

    en.wikipedia.org/wiki/2-Ethylhexanol

    2-Ethylhexanol (abbreviated 2-EH) is an organic compound with the chemical formula C H 3 CH 2 CH 2 CH 2 CH(CH 2 CH 3)CH 2 OH. It is a branched, eight-carbon chiral alcohol . It is a colorless liquid that is poorly soluble in water but soluble in most organic solvents.

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  6. Box Drawing - Wikipedia

    en.wikipedia.org/wiki/Box_Drawing

    Box Drawing is a Unicode block containing characters for compatibility with legacy graphics standards that contained characters for making bordered charts and tables, i.e. box-drawing characters. Its block name in Unicode 1.0 was Form and Chart Components. [3]

  7. Ford, GM donate $1 million and contribute vehicles to Trump's ...

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    DETROIT (Reuters) -U.S. automakers Ford Motor and General Motors will donate $1 million each, along with vehicles, to U.S. President-elect Donald Trump's January inauguration, company ...

  8. Methanesulfonyl chloride - Wikipedia

    en.wikipedia.org/wiki/Methanesulfonyl_chloride

    Methanesulfonyl chloride is mainly used to give methanesulfonates by its reaction with alcohols in the presence of a non-nucleophilic base. [8] In contrast to the formation of toluenesulfonates from alcohols and p-toluenesulfonyl chloride in the presence of pyridine, the formation of methanesulfonates is believed to proceed via a mechanism wherein methanesulfonyl chloride first undergoes an ...

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