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  2. Copper(II) chloride - Wikipedia

    en.wikipedia.org/wiki/Copper(II)_chloride

    The latter process provides a high-yield route to 1,1-binaphthol: [22] Such compounds are intermediates in the synthesis of BINAP and its derivatives. [20] Copper(II) chloride dihydrate promotes the hydrolysis of acetonides, i.e., for deprotection to regenerate diols [23] or aminoalcohols, as in this example (where TBDPS = tert ...

  3. Copper(I) chloride - Wikipedia

    en.wikipedia.org/wiki/Copper(I)_chloride

    IR absorption spectrum of copper(I) chloride. Copper(I) chloride, commonly called cuprous chloride, is the lower chloride of copper, with the formula CuCl.The substance is a white solid sparingly soluble in water, but very soluble in concentrated hydrochloric acid.

  4. Wacker process - Wikipedia

    en.wikipedia.org/wiki/Wacker_process

    Net reaction in the Wacker process. The Wacker process or the Hoechst-Wacker process (named after the chemical companies of the same name) refers to the oxidation of ethylene to acetaldehyde in the presence of palladium(II) chloride and copper(II) chloride as the catalyst. [1]

  5. Copper–chlorine cycle - Wikipedia

    en.wikipedia.org/wiki/Copper–chlorine_cycle

    Simplified diagram of the Copper–Chlorine cycle. The copper–chlorine cycle (Cu–Cl cycle) is a four-step thermochemical cycle for the production of hydrogen. The Cu–Cl cycle is a hybrid process that employs both thermochemical and electrolysis steps.

  6. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75

  7. Sandmeyer reaction - Wikipedia

    en.wikipedia.org/wiki/Sandmeyer_reaction

    [9] [10] [11] [8] The substituted arene is possibly formed by direct transfer of Cl, Br, CN, or OH from a copper(II) species to the aryl radical to produce the substituted arene and regenerate the copper(I) catalyst. In an alternative proposal, a transient copper(III) intermediate, formed from coupling of the aryl radical with the copper(II ...

  8. Gattermann reaction - Wikipedia

    en.wikipedia.org/wiki/Gattermann_reaction

    The Gattermann–Koch reaction, named after the German chemists Ludwig Gattermann and Julius Arnold Koch, [7] is a variant of the Gattermann reaction in which carbon monoxide (CO) is used instead of hydrogen cyanide. [8] Unlike the Gattermann reaction, this reaction is not applicable to phenol and phenol ether substrates. [5]

  9. Dicopper chloride trihydroxide - Wikipedia

    en.wikipedia.org/wiki/Dicopper_chloride_trihydroxide

    Three sixteenths of the Cu atoms are bonded to two near OH groups at 1.93 Å and four stretched OH groups at 2.20 Å to form an axially compressed (2+4) octahedral [Cu(OH) 6], and the remaining one sixteenth of the Cu atoms are bonded to six equivalent OH groups at 2.12 Å to form a regular octahedral [Cu(OH) 6].