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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]
When comparing a polar and nonpolar molecule with similar molar masses, the polar molecule in general has a higher boiling point, because the dipole–dipole interaction between polar molecules results in stronger intermolecular attractions. One common form of polar interaction is the hydrogen bond, which is also
A polar aprotic solvent is a solvent that lacks an acidic proton and is polar. Such solvents lack hydroxyl and amine groups. In contrast to protic solvents, these solvents do not serve as proton donors in hydrogen bonding, although they can be proton acceptors. Many solvents, including chlorocarbons and hydrocarbons, are classifiable as aprotic ...
The most important is dichloromethane, which is mainly used as a solvent. Chloromethane is a precursor to chlorosilanes and silicones. Historically significant (as an anaesthetic), but smaller in scale is chloroform, mainly a precursor to chlorodifluoromethane (CHClF 2) and tetrafluoroethene which is used in the manufacture of Teflon. [2]
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, sweet-smelling, dense liquid produced on a large scale as a precursor to refrigerants and PTFE. [11]
Bromodichloromethane is a trihalomethane with formula C H Br Cl 2.It is a colorless, nonflammable liquid which will dissolve in water, or evaporate in air. [1] Most of the chemical is produced through the chlorine disinfection process, [1] and as a result it can occur in municipally-treated drinking water. [2]
The following table shows that the intuitions from "non-polar", "polar aprotic" and "polar protic" are put numerically – the "polar" molecules have higher levels of δP and the protic solvents have higher levels of δH. Because numerical values are used, comparisons can be made rationally by comparing numbers.
Nonpolar solvent A / solvent B / polymer soluble in solvent B and water / water e.g. heptane, dichloromethane, polyethylene oxide, water; Nonpolar solvent A / solvent B / polymer soluble in solvent B and water / salt / water e.g. 16.3% heptane, 21.7% dichloromethane, 9.5% polyethylene oxide, 51.5% water, 0.1% sodium sulfate