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Equations Sodium carbonate

Equation V-64 is that of a parabola, and electrocapillary curves are indeed approximately parabolic in shape. Because E ax tmd 7 max very nearly the same for certain electrolytes, such as sodium sulfate and sodium carbonate, it is generally assumed that specific adsorption effects are absent, and Emax is taken as a constant (-0.480 V) characteristic of the mercury-water interface. For most other electrolytes there is a shift in the maximum voltage, and is then taken to be Emax 0.480. Some values for the quantities are given in Table V-5 [113]. Much information of this type is due to Gouy [125], although additional results are to be found in most of the other references cited in this section. [Pg.199]

Sodium Hypochlorite. The principal form of hypochlorite produced is sodium hypochlorite [7681-52-9] NaOCl. It is invariably made and used as an aqueous solution and is usually prepared by the chlorination of sodium hydroxide solutions as shown in equation 9, though other bases such as sodium carbonate can be used (30). [Pg.143]

With a reactive solvent, the mass-transfer coefficient may be enhanced by a factor E so that, for instance. Kg is replaced by EKg. Like specific rates of ordinary chemical reactions, such enhancements must be found experimentally. There are no generalized correlations. Some calculations have been made for idealized situations, such as complete reaction in the liquid film. Tables 23-6 and 23-7 show a few spot data. On that basis, a tower for absorption of SO9 with NaOH is smaller than that with pure water by a factor of roughly 0.317/7.0 = 0.045. Table 23-8 lists the main factors that are needed for mathematical representation of KgO in a typical case of the absorption of CO9 by aqueous mouethauolamiue. Figure 23-27 shows some of the complex behaviors of equilibria and mass-transfer coefficients for the absorption of CO9 in solutions of potassium carbonate. Other than Henry s law, p = HC, which holds for some fairly dilute solutions, there is no general form of equilibrium relation. A typically complex equation is that for CO9 in contact with sodium carbonate solutions (Harte, Baker, and Purcell, Ind. Eng. Chem., 25, 528 [1933]), which is... [Pg.2106]

Crystals of sodium hydroxide (lye) react with carbon dioxide from air to form a colorless liquid, water, and a white powder, sodium carbonate, which is commonly added to detergents as a softening agent. Write a balanced equation for this chemical reaction. [Pg.61]

Sodium carbonate is a white powder used in the manufacture of glass. When hydrochloric acid is added to a solution of sodium carbonate, carbon dioxide gas is formed (Figure 8.8). The equation for the reaction is... [Pg.211]

HF appears in this equation because hydrofluoric acid is weak, containing many more HF molecules than H+ ions. Similarly, for the reaction of these two acids with a solution of sodium carbonate ... [Pg.562]

Calculation. The weight of anhydrous sodium carbonate, Na2C03, which has reacted with the standard hydrochloric acid can be readily calculated from the equation ... [Pg.295]

The first report of the use of bromine for the oxidation of sulphoxides appeared in 1966116. Diphenyl sulphone was isolated in 0.5-1% yield when the sulphoxide was treated with bromine in aqueous acetic acid for several hours. The yield was increased to about 5% by quenching the reaction with sodium carbonate. A kinetic study117 of a similar reaction involving dimethyl sulphoxide showed no significant yield improvement but postulated that the mechanism proceeds via an equilibrium step forming a bromosulph-onium type intermediate which reacted slowly with water giving dimethyl sulphone as indicated in equation (35). [Pg.981]

Predicting Write a balanced equation for the reaction that takes place when sodium carbonate and copper(II) sulfate solutions are mixed. [Pg.144]

Hydrolysis of diphenyl phosphorochloridate (DPPC) in 2.0 M aqueous sodium carbonate is also believed to be a two-phase process. DPPC is quite insoluble in water and forms an insoluble second phase at the concentration employed (i.e. 0.10 M). It seems highly significant that the hydrophobic silicon-substituted pyridine 1-oxides (4,6,7) are much more effective catalysts than hydrophilic 8 and 9. In fact, 4 is clearly the most effective catalyst we have examined for this reaction (ti/2 < 10 min). Since derivatives of phosphoric acids are known to undergo substitution reactions via nucleophilic addition-elimination sequences 1201 (Equation 5), we believe that the initial step in hydrolysis of DPPC occurs in the organic phase. Moreover, the... [Pg.206]

Another indispensable carbonate is sodium carbonate, which is also known as soda ash. Centuries ago, impure sodium carbonate was obtained from the places where brine solutions had evaporated and from dry lake beds. The major source of soda ash today is once again from a natural source, but prior to 1985, it was synthesized in large quantities. The synthetic process most often used was the Solvay process, represented by the equations... [Pg.454]

Thus, the equivalent weight of sodium carbonate may be equal to either the formula weight divided by 1 (105.99 g per equivalent, Equation (4.6)) or the formula weight divided by 2 (52.995 g per equivalent, Equation (4.7)), depending on which reaction is involved. [Pg.69]

As stated above, the equivalent weight of sodium carbonate as used in Equation (4.7) is the formula weight divided by 2 because it accepted two hydrogens in the reaction. Thus, utilizing Equation (4.3), we have the following ... [Pg.70]

In a standardization experiment, 0.4920 g of primary standard sodium carbonate (Na2C03) was exactly neutralized by 19.04 mL of hydrochloric acid solution. What is the molarity of the HC1 solution Refer to Equation (4.7) for the reaction involved. [Pg.76]

Which of the following best represents the net ionic equation for the reaction of calcium hydroxide with an aqueous sodium carbonate solution ... [Pg.18]

The indirect method of diazotization is often used for aminoarenesulfonic acids which are relatively insoluble in acid solution where they are present as zwitterions (3 in the case of sulfanilic acid see equation 3). The easily soluble anion 4 is obtained by introducing the required amount of sodium carbonate or hydroxide, and nitrite is added to the approximately neutral solution, which is then run into mineral acid. Indirect diazotization is particularly recommended for the aminosulfonic acids of greater molecular mass but, contrary to some statements in the literature, the three anilinesulfonic acids themselves can be diazotized directly in suspension, the reaction proceeding quite smoothly after some practice. [Pg.630]

The action of the valine derivatives 87 on the diene 86 under EtAlCU catalysis resulted in a mixture of cycloadducts 88, which on hydrolysis with aqueous methanolic sodium carbonate furnished a mixture of the dihydro-2-pyridones 89 and 90 and the esters 91 and 92. In the case of imines derived from aliphatic aldehydes, e.g. 87 (R = Pr), all four types of product were isolated, whereas imines from aromatic aldehydes, 87 (R = Ph, 3-CIC6H4 etc.), gave only the esters 91 and 92 (equation 55). All products were formed in yields of 64-84% and in high de49. [Pg.500]

Treatment of a mixture of a chloro oxime 177 (R = H, Ph, 4-BrCgH4 or 2-furyl) and a diene (cyclopentadiene or 2,3-dimethylbuta-l,3-diene) with solid sodium carbonate results in the formation of a dihydrooxazine, the intermediate nitrosoalkene 178 having reacted as a heterodiene (equation 98)94. In contrast, l,l-dichloro-2-nitrosoethene and cyclopentadiene yield the epoxyepimine 179 (equation 99)94. [Pg.515]

With Carbon,—If caustic soda is heated to dull redness with charcoal or anthracite or some other form of pure carbon, hydrogen is evolved and sodium carbonate and sodium oxide produced, in accordance with the following equation —... [Pg.60]

Wang and Li have reported the determination of procaine hydrochloride injections, and the quality control of 4-aminobenzoic acid [144]. The column packing used for this work consisted of 8 g of silanized siliceous earth support with 5 mL of hexanol as the stationary phase, previously percolated with 20 mL of 0.05 M sodium carbonate. The drug injection solution (containing 10 mg of procaine hydrochloride) was applied to the column, and eluted with 30 mL of 0.05 M sodium carbonate. The eluent was diluted to 50 mL with water, and 4-aminobenzoic acid was determined by an absorbance measurement at 266 nm. Procaine was then eluted from the column using 60 mL of 0.1 M hydrochloric acid. This eluent was treated with 10 mL of acetate buffer (pH 6), and diluted to 100 ml with water. The analyte was determined on the basis of its absorbance at 290 nm. Equations for the computation of procaine and 4-aminobenzoic acid concentrations were presented. [Pg.441]

A range of isothiazolo[5,4-3]pyridines were prepared by cyclization of thiopyridines with iodine/sodium carbonate (Equation 68) <2000FA669>. [Pg.477]

The best way to spot Bronsted-Lowry acids and bases is to keep careful track of hydrogen ions in a chemical equation. Consider, for example, the dissociation of the base sodium carbonate in water. Note that although sodium carbonate is a base, it doesn t contain a hydroxide ion. [Pg.225]

Pour 2-3 ml of a 1 N sodium hydroxide solution into a test tube and pass carbon(IV) oxide through it until the solution becomes almost neutral. Heat the solution. What gas evolves After this, test the reaction of the solution with indicators. Write the equations of the reactions and explain the difierence in the action of the solutions on indicators. What salt hydrolyzes more—sodium carbonate or bicarbonate Why ... [Pg.163]

See how the carbonates of various metals change when heated. For this purpose, roast the following salts in test tubes basic copper carbonate, magnesium, calcium, and sodium carbonates, and sodium bicarbonate. Pass the evolving gas into lime water. Write the equations of the reactions. Explain why the thermal stability of the studied carbonates differs. [Pg.163]

Lithium Carbonate. Add a saturated sodium carbonate solution to 2-3 ml of a saturated lithium sulphate or chloride solution. What do you observe Write the equation of the reaction. Acquaint yourself with the solubility of the alkali metal carbonates in water. [Pg.183]

Magnesium Basic Carbonate (Magnesia Alba). Add a sodium carbonate solution to a magnesium sulphate or chloride solution heated to 50 °C up to complete precipitation. What is the composition of the precipitate Filter off the latter, wash it with water, and dry it in a drying cabinet at 100-150 °C. Heat the filtrate up to boiling. What do you observe Write the equations of the reactions. [Pg.191]

Add an equal volume of a sodium carbonate solution to a cerium nitrate one, next add dropwise a potassium permanganate solution. What is the composition of the precipitate Write the equation of the reaction. [Pg.206]

Preparation of Sodium Vanadate. Put a thoroughly triturated mixture of 0.5 g of vanadium(V) oxide and 1 g of sodium carbonate into a crucible and place it into a crucible furnace. Raise the furnace temperature to 800 °C and control the course of the process. Lower the hot crucible into a beaker with water to separate the melt easily from the crucible walls. Crush the melt in a mortar and treat it with water while heating. Evaporate the solution until crystallization begins. Examine the crystals under a microscope. Write the equation of the reaction. [Pg.212]


See other pages where Equations Sodium carbonate is mentioned: [Pg.317]    [Pg.197]    [Pg.115]    [Pg.1038]    [Pg.425]    [Pg.732]    [Pg.64]    [Pg.70]    [Pg.107]    [Pg.127]    [Pg.443]    [Pg.225]    [Pg.720]    [Pg.731]    [Pg.732]    [Pg.762]    [Pg.203]   
See also in sourсe #XX -- [ Pg.286 ]




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