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Solid-forming solutions

In the next chapter, we look at some other solid-forming solutions, as well as some whys, wherefores, and useful applications of these crusty precipitation reactions. [Pg.94]

S02NH) . Colourless crystalline solids formed by the action of ammonia on a solution of sulphuryl chloride in benzene free sulphimide exists only in the polymerized form. [Pg.376]

Vanadium ni) chloride, VCI3. Violet solid formed V plus HCl gas. VCIj bHiO formed from solution. Forms many complexes. [Pg.417]

What if the analyte is an aqueous ion, such as Pb + In this case we cannot isolate the analyte by filtration because the Pb + is dissolved in the solution s matrix. We can still measure the analyte s mass, however, by chemically converting it to a solid form. If we suspend a pair of Pt electrodes in our solution and apply a sufficiently positive potential between them for a long enough time, we can force the reaction... [Pg.233]

Inclusions, occlusions, and surface adsorbates are called coprecipitates because they represent soluble species that are brought into solid form along with the desired precipitate. Another source of impurities occurs when other species in solution precipitate under the conditions of the analysis. Solution conditions necessary to minimize the solubility of a desired precipitate may lead to the formation of an additional precipitate that interferes in the analysis. For example, the precipitation of nickel dimethylgloxime requires a plT that is slightly basic. Under these conditions, however, any Fe + that might be present precipitates as Fe(01T)3. Finally, since most precipitants are not selective toward a single analyte, there is always a risk that the precipitant will react, sequentially, with more than one species. [Pg.239]

The washed benzene layer is diluted with an equal volume of ether and alcoholic hydrochloric acid is added until the mixture is acid to Congo red. A white crystalline solid forms which is dissolved in 300-400 cc of alcohol and diluted with ether to the point where precipitation starts. A few drops of butanone are added, the solution is cooled to -10°C, and filtered to recover the crystals which separate. The product is obtained in the form of white needles melting at IbS -IBO C, in good yield. [Pg.478]

One part by weight of propyl-methyl-carbinyl allyl barbituric acid is added to enough alcohol to facilitate handling, in this case conveniently about six times its weight. To this is added a solution of sodium hydroxide, preferably carbonate-free or substantially so, containing °%38 parts by weight of sodium hydroxide, which is the amount of sodium hydroxide necessary to combine in equal molecular proportions with the propyl-methyl-carbinyl allyl barbituric acid. This solution is filtered clear, and is then evaporated under vacuum until the sodium propyl-methyl-carbinyl allyl barbiturate (alternatively named sodium allyl 1-methyl-butyl barbiturate) separates out in solid form. The salt as thus obtained in solid form contains a varying amount of moisture. [Pg.1370]

At the same time it is recognized that the pairs of substances which, on mixing, are most likely to obey Raoult s law are those whose particles are most nearly alike and therefore interchangeable. Obviously no species of particles is likely to fulfill this condition better than the isotopes of an element. Among the isotopes of any element the only difference between the various particles is, of course, a nuclear difference among the isotopes of a heavy element the mass difference is trivial and the various species of particles are interchangeable. Whether the element is in its liquid or solid form, the isotopes of a heavy element form an ideal solution. Before discussing this problem we shall first consider the solution of a solid solute in a liquid solvent. [Pg.81]

If Q < Ksp, the solution contains a lower concentration of ions than is required for equilibrium with the solid. The solution is unsaturated. No precipitate forms equilibrium is not established. [Pg.433]

Complete the next three figures below by filling one-liter boxes to the right of the arrow, showing the state of the ions after water is added to form saturated solutions. The species represented to the left of the arrow is the solid form of the ions represented above. Do not show the water molecules. [Pg.448]

Discussion. Most hypochlorites are normally obtained only in solution, but calcium hypochlorite exists in the solid form in commercial bleaching powder which consists essentially of a mixture of calcium hypochlorite Ca(OCl)2 and the basic chloride CaCl2,Ca(0H)2,H20 some free slaked lime is usually present. The active constituent is the hypochlorite, which is responsible for the bleaching action. Upon treating bleaching powder with hydrochloric acid, chlorine is liberated ... [Pg.396]

Let the system consist of a binary liquid solution in equilibrium with the solid form of one substance in the pure state. We have then, if the doubly-accented symbols refer to the solid ... [Pg.418]

Sodium hypochlorite is usually sold in solution in water, where it makes a greenish-yellow liquid. (It is too hygroscopic—it absorbs water from the air—to be used conveniently in solid form.) Household bleaches usually contain sodium hypochlorite in a 3 percent to 6 percent solution. Some sodium hydroxide (lye) is added to keep the pH high to avoid decomposition. If the solution is made more acidic, sodium hypochlorite will dissociate, producing chlorine gas and oxygen. [Pg.191]

When we mix two solutions the result is often simply a new solution that contains both solutes. However, in some cases the solutes can react with each other. For instance, when we mix a colorless aqueous solution of silver nitrate with a clear yellow aqueous solution of potassium chromate, a red solid forms, indicating that a chemical reaction has occurred (Fig. 1.1). This section and the next two introduce three of the main types of chemical reactions precipitation reactions, acid-base reactions, and redox reactions, all of which are discussed in more depth in later chapters. (The fourth type of reaction discussed in this text, Lewis acid-base reactions, is introduced in Section 10.2.) Because many chemical reactions take place in solution, particularly in water, in this section we begin by considering the nature of aqueous solutions. [Pg.90]

K, = 7.8 X 10 4, is usually marketed as the hydrogen bromide salt, C6H5CH2CH(CH )NH3+Br, because it is much more stable in this solid form. Determine the pH of a solution made from dissolving 6.48 g of the salt to form 200.0 mL of solution. [Pg.561]

Complexes of molybdenum in the lower valence-states of -t 2 and + 3 have been produced only in the past two years. For the Mo(II) species, the usual starting-material is Mo2(acetate>4. Reaction of this with KS2COEt in THF gives two products, a green complex tentatively assigned as [Mo2(Etxant>4], which solvates to form the red complex [Mo2(Etxant)4(THF)2]. The structure of the latter complex was elucidated by X-ray analysis 169). Steele and Stephenson 170) were also able to synthesize a red, crystalline solid (methanol solution), which they formulated as [Mo(Etxant)2]2 (XI), and reacted this with Lewis bases, e.g., pyridine, to form [Mo(Etxant)2L]2- Thus, there appears to be a difference between the two compounds formulated as [Mo2(Et-xant)2]2 that... [Pg.229]

The alkali-catalysed methanolysis of poly(2,2-bis(4-hydroxyphenyljpropane carbonate) (PC) in a mixture of methanol (MeOH) and toluene or dioxane was studied. The treatment of PC in meOH, with a catalytic amount of sodium hydroxide, yielded only 7% bisphenol A. Using a mixed solvent of MeOH and toluene completely depolymerised PC to give 96% free bisphenol A in solid form and dimethyl carbonate in solution. The eharaeteristies of the catalysis are discussed together with the pseudo-first rate kinetics of the depolymerisation. The reaetion eonditions were investigated to facilitate the reeyeling of PC plasties. 17 refs. [Pg.64]

The stability of phosphinous amides depends, to a large extent, on the substituents at phosphorus and nitrogen. Normally, tetrasubstituted and N,P,P-trisubstituted phosphinous amides are stable and well-known compounds. The parent compound H2PNH2 is a volatile compound that is formed on hydrolysis of a solid state solution mixture of magnesium phosphide and magnesium... [Pg.79]

C04-0089. If 75.0 mL of a 0.750 M solution of lead(II) nitrate is mixed with 125 mL of 0.855 M ammonium chloride, what mass of solid forms, and what ions remain in solution ... [Pg.268]

Water is highly polar, but it is not ionic. How, then, can water act as a solvent for ionic solids A salt dissolves only if the interactions between the ions and the solvent are strong enough to overcome the attractive forces that hold ions in the ciystal lattice. When an ionic solid forms an aqueous solution, the cations and anions are solvated by strong ion-dipole interactions with water molecules. [Pg.843]


See other pages where Solid-forming solutions is mentioned: [Pg.194]    [Pg.49]    [Pg.194]    [Pg.49]    [Pg.117]    [Pg.212]    [Pg.266]    [Pg.185]    [Pg.35]    [Pg.107]    [Pg.418]    [Pg.112]    [Pg.188]    [Pg.50]    [Pg.509]    [Pg.874]    [Pg.83]    [Pg.72]    [Pg.345]    [Pg.638]    [Pg.937]    [Pg.1047]    [Pg.882]    [Pg.770]    [Pg.394]    [Pg.360]    [Pg.377]    [Pg.816]    [Pg.962]    [Pg.138]    [Pg.156]    [Pg.63]   
See also in sourсe #XX -- [ Pg.94 ]




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Ions forming solid solutions

Solid forms

System in which the two components form a continuous series of solid solutions

Systems that Form Solid Solutions

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