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It is less volatile than chloroform, therefore it was more difficult to apply and needed warm water to evaporate. [55] Its smell has been described as "fruity", [55] quince-like [57] and "more pleasant than chloroform", [51] and had a "pleasant taste". [55] Carbon tetrachloride for anaesthetic use was made by the chlorination of carbon disulfide.
Due to the polar nature of the water molecule itself, other polar molecules are generally able to dissolve in water. Most nonpolar molecules are water-insoluble (hydrophobic) at room temperature. Many nonpolar organic solvents, such as turpentine, are able to dissolve nonpolar substances.
Solvents can be broadly classified into two categories: polar and non-polar. A special case is elemental mercury, whose solutions are known as amalgams; also, other metal solutions exist which are liquid at room temperature. Generally, the dielectric constant of the solvent provides a rough measure of a solvent's polarity.
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
CCL4 is a polypeptide chain with a molecular weight of approximately 8-10 kDa [10] arranged in a three-dimensional structure in the form of as symmetrical homodimer. Monomeric subunits in their secondary structure composed by a triple-stranded antiparallel sheet form in a Greek key structure on top of which lies an α-helix.
Dichloromethane (DCM, methylene chloride, or methylene bichloride) is an organochlorine compound with the formula C H 2 Cl 2. This colorless, volatile liquid with a chloroform-like, sweet odor is widely used as a solvent. Although it is not miscible with water, it is slightly polar, and miscible with many organic solvents. [12]
Carbon tetraiodide is slightly reactive towards water, giving iodoform and I 2. It is soluble in nonpolar organic solvents. It decomposes thermally and photochemically to tetraiodoethylene, C 2 I 4. Its synthesis entails AlCl 3-catalyzed halide exchange, which is conducted at room temperature: [4] CCl 4 + 4 EtI → CI 4 + 4 EtCl
The two main groups of organochlorine insecticides are the DDT-type compounds and the chlorinated alicyclics. Their mechanism of action differs slightly. The DDT like compounds work on the peripheral nervous system. At the axon's sodium channel, they prevent gate closure after activation and membrane depolarization. Sodium ions leak through the ...