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Adsorption removes a soluble impurity from a feed stream by trapping it on the surface of a solid material, such as activated carbon, that forms strong non-covalent chemical bonds with the impurity. Chromatography employs continuous adsorption and desorption on a packed bed of a solid to purify multiple components of a single feed stream. In a ...
The solvent utilized in single-solvent recrystallization must dissolve the crude reaction mixture only when it is heated to reflux. [3] The heated solution is then passively cooled, yielding a crystallized product absent of impurities. [3] The solid crystals are then collected utilizing a filtration apparatus and the filtrate is discarded. [4]
Although the original process involves water, a green solvent itself, sc-CO 2 allows less waste materials. [57] In deep eutectic solvents, observations report that the higher the solvent's hydrophobicity, the higher the extraction efficiency of neonicotinoids from aqueous solutions, although the exact trend has not been established yet. [58]
A solvent is chosen in which the desired product is insoluble and the undesired by-products are very soluble or vice versa. For example, when the impurities are soluble and the desired product is not, the crude material is washed with the solvent and filtered, leaving the purified product in solid form and any impurities in solution.
It is a white extremely hygroscopic solid that is soluble in water, alcohols, and other polar organic solvents. [6] The CH 3 C 6 H 4 SO 2 group is known as the tosyl group and is often abbreviated as Ts or Tos. Most often, TsOH refers to the monohydrate, TsOH. H 2 O. [6] As with other aryl sulfonic acids, TsOH is a strong organic acid.
Deep eutectic solvents or DESs are solutions of Lewis or Brønsted acids and bases which form a eutectic mixture. [1] Deep eutectic solvents are highly tunable through varying the structure or relative ratio of parent components and thus have a wide variety of potential applications including catalytic, separation, and electrochemical processes.
Although DCM is a common solvent in organic chemistry laboratories and is commonly assumed to be inert, it does react with some amines and triazoles. [21] Tertiary amines can react with DCM to form quaternary chloromethyl chloride salts via the Menshutkin reaction . [ 22 ]
Protic solvents react with strong nucleophiles with good basic character in an acid/base fashion, thus decreasing or removing the nucleophilic nature of the nucleophile. The following table shows the effect of solvent polarity on the relative reaction rates of the S N 2 reaction of 1-bromobutane with azide (N 3 –). There is a noticeable ...