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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. 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.

  5. 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

  6. Van der Waals constants (data page) - Wikipedia

    en.wikipedia.org/wiki/Van_der_Waals_constants...

    Cyclopropane [2] 8.34 0.0747 Decane [2] 52.74 0.3043 1-Decanol [2] 59.51 0.3086 Diethyl ether: 17.61 0.1344 Diethyl sulfide: 19.00 0.1214 Dimethyl ether: 8.180 0.07246 Dimethyl sulfide: 13.04 0.09213 Dodecane [2] 69.38 0.3758 1-Dodecanol [2] 75.70 0.3750 Ethane: 5.562 0.0638 Ethanethiol: 11.39 0.08098 Ethanol: 12.18 0.08407 Ethyl acetate: 20.72 ...

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    Chronic diseases related to diet, like type 2 diabetes, heart disease and some types of cancer, are widespread. More than three-quarters of Americans eat more saturated fat, typically from red ...

  9. 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]