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  2. Polar aprotic solvent - Wikipedia

    en.wikipedia.org/wiki/Polar_aprotic_solvent

    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 ...

  3. Protic solvent - Wikipedia

    en.wikipedia.org/wiki/Protic_solvent

    The molecules of such solvents readily donate protons (H +) to solutes, often via hydrogen bonding. Water is the most common protic solvent. Conversely, polar aprotic solvents cannot donate protons but still have the ability to dissolve many salts. [1] [2] Methods for purification of common solvents are available [3]

  4. Solvent - Wikipedia

    en.wikipedia.org/wiki/Solvent

    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.

  5. Solvation - Wikipedia

    en.wikipedia.org/wiki/Solvation

    Solvents that can donate H-bonds are referred to as protic, while solvents that do not contain a polarized bond to a hydrogen atom and cannot donate a hydrogen bond are called aprotic. H-bond donor ability is classified on a scale (α). [6] Protic solvents can solvate solutes that can accept hydrogen bonds. Similarly, solvents that can accept a ...

  6. Inorganic nonaqueous solvent - Wikipedia

    en.wikipedia.org/wiki/Inorganic_nonaqueous_solvent

    An inorganic nonaqueous solvent is a solvent other than water, that is not an organic compound. These solvents are used in chemical research and industry for reactions that cannot occur in aqueous solutions or require a special environment. Inorganic nonaqueous solvents can be classified into two groups, protic solvents and aprotic solvents.

  7. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    This difference arises from acid/base reactions between protic solvents (not aprotic solvents) and strong nucleophiles. While it is true that steric effects also affect the relative reaction rates, [ 12 ] however, for demonstration of principle for solvent polarity on S N 2 reaction rates, steric effects may be neglected.

  8. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    Solvent Density (g cm-3) Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: 184.3 3.69 –5.96 –5.87 K b & K f [1 ...

  9. Dimethyl sulfoxide - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfoxide

    Dimethyl sulfoxide (DMSO) is an organosulfur compound with the formula (CH 3) 2 S O.This colorless liquid is the sulfoxide most widely used commercially. It is an important polar aprotic solvent that dissolves both polar and nonpolar compounds and is miscible in a wide range of organic solvents as well as water.