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  2. Ethylmagnesium bromide - Wikipedia

    en.wikipedia.org/wiki/Ethylmagnesium_bromide

    Ethylmagnesium bromide is commercially available, usually as a solution in diethyl ether or tetrahydrofuran. It may be prepared in the normal manner of Grignard reagents — by reacting bromoethane with magnesium in diethyl ether: [2] EtBr + Mg → EtMgBr

  3. Bromoethane - Wikipedia

    en.wikipedia.org/wiki/Bromoethane

    Bromoethane, also known as ethyl bromide, is a chemical compound of the haloalkanes group. It is abbreviated by chemists as EtBr (which is also used as an abbreviation for ethidium bromide ). This volatile compound has an ether-like odor.

  4. Grignard reagent - Wikipedia

    en.wikipedia.org/wiki/Grignard_reagent

    Water and air, which rapidly destroy the reagent by protonolysis or oxidation, are excluded. [1] Although the reagents still need to be dry, ultrasound can allow Grignard reagents to form in wet solvents by activating the magnesium such that it consumes the water. [2]

  5. Michael addition reaction - Wikipedia

    en.wikipedia.org/wiki/Michael_Addition_Reaction

    For example, the image below shows the addition of ethylmagnesium bromide to ethyl sorbate 1 using a copper catalyst with a reversed josiphos (R,S)-(–)-3 ligand. [35] This reaction produced the 1,6-addition product 2 in 0% yield, the 1,6-addition product 3 in approximately 99% yield, and the 1,4-addition product 4 in less than 2%

  6. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  7. Kulinkovich reaction - Wikipedia

    en.wikipedia.org/wiki/Kulinkovich_reaction

    The Kulinkovich reaction describes the organic synthesis of substituted cyclopropanols through reaction of esters with dialkyl­dialkoxy­titanium reagents, which are generated in situ from Grignard reagents containing a hydrogen in beta-position and titanium(IV) alkoxides such as titanium isopropoxide. [1]

  8. Dimethylmagnesium - Wikipedia

    en.wikipedia.org/wiki/Dimethylmagnesium

    2 CH 3 MgX + 2 dioxane ⇌ (CH 3) 2 Mg + MgX 2 (μ-dioxane) 2 ↓. In such procedures, the dimethylmagnesium exists as the ether adduct, not the polymer. [4] Addition of 1,4-dioxane causes precipitation of solid MgX 2 (μ-dioxane) 2, a coordination polymer. [4] This precipitation drives the Schlenk equilibrium toward (CH 3) 2 Mg. Related ...

  9. 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