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Drying agents for organic compounds

Tabi.e II, 39. CojraiON Drying Agents for Organic Compounds... [Pg.144]

Table 2.9 Common drying agents for organic compounds ... Table 2.9 Common drying agents for organic compounds ...
Magnesium methylate is used as a drying agent for alcohols and other organic solvents and as an intermediate in various manufacturing processes, eg, for organomagnesium compounds (79), orthocarbonic esters (80), and for oxide coatings. [Pg.27]

Wash the organic layer two times with 10-mL portions of 5% aqueous sodium bicarbonate solution. Then wash the organic layer with an equal volume of water. If an emulsion forms, use a little saturated sodium chloride solution to break it. Dry the organic layer over anhydrous sodium sulfate for 10-15 minutes. After the dried solution is removed from the drying agent, the organic layer should contain only Compound 1 and methylene chloride. Isolate Compoimd 1 by removing the methylene chloride. [Pg.549]

The ethereal extracts are then united, dried with a suitable drying agent and filtered. The filtrate is then cautiously distilled, the ether being first distilled and finally the organic compound if volatile if the compound is solid, the crude residue is purified by recrystallisation. Very great care must be taken on all occasions when ether is distilled because of the risk of fire or of an explosion full experimental details for this operation are given, both on p. 8o (Preparation of Ether) and on p. 164 (Pre-... [Pg.35]

We may now understand the nature of the change which occurs when an anhydrous salt, say copper sulphate, is shaken with a wet organic solvent, such as benzene, at about 25°. The water will first combine to form the monohydrate in accordance with equation (i), and, provided suflScient anhydrous copper sulphate is employed, the effective concentration of water in the solvent is reduced to a value equivalent to about 1 mm. of ordinary water vapour. The complete removal of water is impossible indeed, the equilibrium vapour pressures of the least hydrated tem may be taken as a rough measure of the relative efficiencies of such drying agents. If the water present is more than sufficient to convert the anhydrous copper sulphate into the monohydrate, then reaction (i) will be followed by reaction (ii), i.e., the trihydrate will be formed the water vapour then remaining will be equivalent to about 6 mm. of ordinary water vapour. Thus the monohydrate is far less effective than the anhydrous compound for the removal of water. [Pg.41]

The common drying agents that are suitable for various classes of organic compounds are listed in Table II, 39. [Pg.143]


See other pages where Drying agents for organic compounds is mentioned: [Pg.358]    [Pg.358]    [Pg.5]    [Pg.55]    [Pg.61]    [Pg.49]    [Pg.30]    [Pg.49]    [Pg.3]    [Pg.55]    [Pg.5]    [Pg.63]    [Pg.73]    [Pg.73]    [Pg.407]    [Pg.84]    [Pg.176]    [Pg.150]    [Pg.67]    [Pg.67]    [Pg.407]    [Pg.395]    [Pg.406]    [Pg.395]    [Pg.294]    [Pg.77]    [Pg.177]    [Pg.22]    [Pg.84]    [Pg.25]    [Pg.90]    [Pg.214]    [Pg.105]    [Pg.199]    [Pg.538]    [Pg.228]    [Pg.171]    [Pg.130]    [Pg.9]   
See also in sourсe #XX -- [ Pg.43 ]




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Drying agents

Drying organic compounds

Drying: agents for

Organic agents

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