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Chloroform, [10] or trichloromethane (often abbreviated as TCM), is an organochloride with the formula C H Cl 3 and a common solvent. It is a volatile, colorless ...
This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.
log 10 of Chloroform vapor pressure. Uses formula: log e P m m H g = {\displaystyle \scriptstyle \log _{e}P_{mmHg}=} log e ( 760 101.325 ) − 10.07089 log e ( T + 273.15 ) − 6351.140 T + 273.15 + 81.14393 + 9.127608 × 10 − 6 ( T + 273.15 ) 2 {\displaystyle \scriptstyle \log _{e}({\frac {760}{101.325}})-10.07089\log _{e}(T+273. ...
Only chloroform has significant applications of the haloforms. In the predominant application, chloroform is required for the production of tetrafluoroethylene (TFE), precursor to teflon . [ 1 ] Chloroform is fluorinated by reaction with hydrogen fluoride to produce chlorodifluoromethane (R-22).
The most common substrates are chlorinated aliphatics (PCE, TCE, chloroform) and chlorinated phenols. Organohalide-respiring bacteria are highly diverse. This trait is found in some Campylobacterota, Thermodesulfobacteriota, Chloroflexota (green nonsulfur bacteria), low G+C gram positive Clostridia, [4] and ultramicrobacteria.
Samuel Guthrie was born in Brimfield, in Hampden's county, Massachusetts, in 1782 [1] "Dr. Guthrie was of dark complexion, medium stature, slender build, slightly stooping figure, and thoughtful mien; his head was well-formed and of full medium size, features slightly oval, nose prominent and a little irregular in shape."
In chemistry, the haloform reaction (also referred to as the Lieben haloform reaction) is a chemical reaction in which a haloform (CHX 3, where X is a halogen) is produced by the exhaustive halogenation of an acetyl group (R−C(=O)CH 3, where R can be either a hydrogen atom, an alkyl or an aryl group), in the presence of a base.
The output of these processes is a mixture of chloromethane, dichloromethane, chloroform, and carbon tetrachloride as well as hydrogen chloride as a byproduct.