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  2. Ethyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_sulfate

    ch 3 ch 2 oh + h 2 so 4 → ch 3 ch 2 oso 3 h + h 2 o If the temperature exceeds 140 °C, the ethyl sulfate product tends to react with residual ethanol starting material, producing diethyl ether . If the temperature exceeds 170 °C in a considerable excess of sulfuric acid, the ethyl sulfate breaks down into ethylene and sulfuric acid.

  3. Diethyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Diethyl_sulfate

    Although the formula for diethyl sulfate is typically written (C 2 H 5) 2 SO 4, a more descriptive formula would be (C 2 H 5 O) 2 SO 2. It is a diester of sulfuric acid. Sulfur is tetrahedral. Diethyl sulfate hydrolyzes readily, forming ethanol and ethyl sulfate. Eventually sulfuric acid is formed with excess water.

  4. Triethyloxonium tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Triethyloxonium_tetrafluo...

    Triethyloxonium tetrafluoroborate is the organic oxonium compound with the formula [(CH 3 CH 2) 3 O] + [BF 4] −. It is often called Meerwein's reagent or Meerwein's salt after its discoverer Hans Meerwein. [2] [3] Also well known and commercially available is the related trimethyloxonium tetrafluoroborate. The compounds are white solids that ...

  5. Organosulfate - Wikipedia

    en.wikipedia.org/wiki/Organosulfate

    In organosulfur chemistry, organosulfates are a class of organic compounds sharing a common functional group with the structure R−O−SO − 3. The SO 4 core is a sulfate group and the R group is any organic residue. All organosulfates are formally esters derived from alcohols and sulfuric acid (H 2 SO 4) although many

  6. Ethanethiol - Wikipedia

    en.wikipedia.org/wiki/Ethanethiol

    Ethanethiol, commonly known as ethyl mercaptan, is an organosulfur compound with the formula CH 3 CH 2 SH. [5] It is a colorless liquid with a distinct odor. Abbreviated EtSH, it consists of an ethyl group (Et), CH 3 CH 2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with sulfur in place of oxygen. The odor of ...

  7. Color Developing Agent 3 - Wikipedia

    en.wikipedia.org/wiki/Color_Developing_Agent_3

    The third in the series of color developing agents used in developing color films, commonly known as CD-3, is chemically known as N-[2-[(4-Amino-3-methylphenyl)ethylamino]ethyl]methanesulfonamide Sesquisulfate Monohydrate. [1]

  8. Propionitrile - Wikipedia

    en.wikipedia.org/wiki/Propionitrile

    ch 3 ch 2 ch 2 oh + o 2 + nh 3 → ch 3 ch 2 c≡n + 3 h 2 o Propionitrile is a byproduct of the electrodimerisation of acrylonitrile to adiponitrile . In the laboratory propanenitrile can also be produced by the dehydration of propionamide , by catalytic reduction of acrylonitrile , or by distilling ethyl sulfate and potassium cyanide .

  9. Tetraethylammonium - Wikipedia

    en.wikipedia.org/wiki/Tetraethylammonium

    Tetraethylammonium (TEA) is a quaternary ammonium cation with the chemical formula [Et 4 N] +, consisting of four ethyl groups (−C 2 H 5, denoted Et) attached to a central nitrogen atom. It is a counterion used in the research laboratory to prepare lipophilic salts of inorganic anions.