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  2. Acetonitrile - Wikipedia

    en.wikipedia.org/wiki/Acetonitrile

    Acetonitrile is used mainly as a solvent in the purification of butadiene in refineries. Specifically, acetonitrile is fed into the top of a distillation column filled with hydrocarbons including butadiene, and as the acetonitrile falls down through the column, it absorbs the butadiene which is then sent from the bottom of the tower to a second separating tower.

  3. Acetonitrile (data page) - Wikipedia

    en.wikipedia.org/wiki/Acetonitrile_(data_page)

    log 10 of Acetonitrile vapor pressure. Uses formula log e ⁡ P m m H g = {\displaystyle \scriptstyle \log _{e}P_{mmHg}=} log e ⁡ ( 760 101.325 ) − 3.881710 log e ⁡ ( T + 273.15 ) − 4999.618 T + 273.15 + 41.05901 + 3.515956 × 10 − 06 ( T + 273.15 ) 2 {\displaystyle \scriptstyle \log _{e}({\frac {760}{101.325}})-3.881710\log _{e}(T+ ...

  4. Chloroacetonitrile - Wikipedia

    en.wikipedia.org/wiki/Chloroacetonitrile

    A colorless liquid, it is derived from acetonitrile (CH 3 CN) by replacement of one H with Cl. In practice, it is produced by dehydration of chloroacetamide. [1] The compound is an alkylating agent, [2] and as such is handled cautiously. Chloroacetonitrile is also generated in situ by the reaction of acetonitrile with sulfur monochloride.

  5. Trichloroacetonitrile - Wikipedia

    en.wikipedia.org/wiki/Trichloroacetonitrile

    Trichloroacetonitrile can be obtained by chlorination of acetonitrile on a zinc, copper and alkaline earth metal halide-impregnated activated carbon catalyst at 200–400 °C with a 54% yield. [ 3 ] The high temperatures required by this process favours the formation of byproducts, such as tetrachloromethane .

  6. Tetrabutylammonium hexafluorophosphate - Wikipedia

    en.wikipedia.org/wiki/Tetrabutylammonium_hexaflu...

    It is highly soluble in polar organic solvents such as acetone and acetonitrile. The salt consists of a positively charged tetrabutylammonium, a quaternary ammonia cation and a weakly basic hexafluorophosphate anion. These species are chemically inert, which allows the salt to serve as an inert electrolyte over a wide potential range.

  7. 1,8-Diazabicyclo(5.4.0)undec-7-ene - Wikipedia

    en.wikipedia.org/wiki/1,8-Diazabicyclo(5.4.0...

    CAS Number. 6674-22-2 ... 24.34 [2] (pK a of conjugate acid in acetonitrile) Hazards GHS labelling: Pictograms. Signal word. Danger: Hazard statements.

  8. NYT ‘Connections’ Hints and Answers Today, Sunday, December 15

    www.aol.com/nyt-connections-hints-answers-today...

    Read no further until you really want some clues or you've completely given up and want the answers ASAP. Get ready for all of today's NYT 'Connections’ hints and answers for #553 on Sunday ...

  9. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH 3) 2 CO. [22] It is the simplest and smallest ketone (>C=O).It is a colorless, highly volatile, and flammable liquid with a characteristic pungent odour, very reminiscent of the smell of pear drops.