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  2. Simmons–Smith reaction - Wikipedia

    en.wikipedia.org/wiki/Simmons–Smith_reaction

    The Charette modification replaces the CH 2 I 2 normally found in the Simmons–Smith reaction with aryldiazo compounds, such as phenyldiazomethane, in Pathway A. [30] Upon treatment with stoichiometric amounts of zinc halide, an organozinc compound similar to the carbenoid discussed above is produced. This can react with almost all alkenes and ...

  3. Zinc compounds - Wikipedia

    en.wikipedia.org/wiki/Zinc_compounds

    Zinc is a strong reducing agent with a standard redox potential of −0.76 V. Pure zinc tarnishes rapidly in air, rapidly forming a passive layer. The composition of this layer can be complex, but one constituent is probably basic zinc carbonate, Zn 5 (OH) 6 CO 3. [8] The reaction of zinc with water is slowed by this passive layer.

  4. Organozinc chemistry - Wikipedia

    en.wikipedia.org/wiki/Organozinc_chemistry

    The reaction produces a primary, secondary, or tertiary alcohol via a 1,2-addition. The Barbier reaction is advantageous because it is a one-pot process: the organozinc reagent is generated in the presence of the carbonyl substrate. Organozinc reagents are also less water sensitive, thus this reaction can be conducted in water.

  5. Zinc cyanide - Wikipedia

    en.wikipedia.org/wiki/Zinc_cyanide

    Zn(CN) 2 is easy to make by combining aqueous solutions of cyanide and zinc ions, for example via the double replacement reaction between KCN and ZnSO 4: [5] ZnSO 4 + 2 KCN → Zn(CN) 2 + K 2 SO 4. For commercial applications, some effort is made to avoid halide impurities by using acetate salts of zinc: [5] [6] Zn(CH 3 COO) 2 + HCN → Zn(CN ...

  6. Reformatsky reaction - Wikipedia

    en.wikipedia.org/wiki/Reformatsky_reaction

    The Reformatsky reaction (sometimes transliterated as Reformatskii reaction) is an organic reaction which condenses aldehydes or ketones with α-halo esters using metallic zinc to form β-hydroxy-esters: [1] [2] The Reformatsky reaction. The organozinc reagent, also called a 'Reformatsky enolate', is prepared by treating an alpha-halo ester ...

  7. Decamethyldizincocene - Wikipedia

    en.wikipedia.org/wiki/Decamethyldizincocene

    The relative amounts depend on reaction conditions, which can be optimized to favor one or the other. [2] For instance, if this reaction is conducted in pentane at -40 °C, (η 5-C 5 Me 5)ZnEt is the sole product. Conversely, if the reaction is conducted in diethyl ether at -10 °C, (Zn 2 (η 5-C 5 Me 5) 2) is the major product.

  8. Solubility chart - Wikipedia

    en.wikipedia.org/wiki/Solubility_chart

    The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.

  9. Water-reactive substances - Wikipedia

    en.wikipedia.org/wiki/Water-reactive_substances

    Water-reactive substances [1] are those that spontaneously undergo a chemical reaction with water, often noted as generating flammable gas. [2] Some are highly reducing in nature. [ 3 ] Notable examples include alkali metals , lithium through caesium , and alkaline earth metals , magnesium through barium .