Silver chloride nitrate

Addition of silver nitrate to a solution of a chloride in dilute nitric acid gives a white precipitate of silver chloride, AgCl, soluble in ammonia solution. This test may be used for gravimetric or volumetric estimation of chloride the silver chloride can be filtered off, dried and weighed, or the chloride titrated with standard silver nitrate using potassium chromate(VI) or fluorescein as indicator. 

Addition of silver nitrate to a solution of a bromide in nitric acid produces a cream-coloured precipitate of silver bromide, soluble in ammonia (but not so readily as silver chloride). The reaction may be used quantitatively, as for a chloride. 

A compound of cobalt has the formula Co(NH3)jtCl. 0.500 g of it was dissolved in 50.00 cm M hydrochloric acid the excess acid required 40.00 cm M sodium hydroxide solution to neutralise it. Another 0.500 g portion of the compound was dissolved in water and allowed to react with excess silver nitrate solution. 0.575 g of silver chloride was precipitated. 

All the silver halides are sensitive to light, decomposing eventually to silver. In sunlight, silver chloride turns first violet and finally black. The use of these compounds in photography depends on this (see below). (All silver salts are, in fact, photosensitive—the neck of a silver nitrate bottle is black owing to a deposit of silver.)... 

Add a few drops of the distillate to an aqueous silver nitrate solution containing some dilute nitric acid and warm gently no silver chloride should be precipitated, indicating the complete absence of unchanged acetyl chloride. 

Silver Bromide. Silver bromide, AgBr, is formed by the addition of bromide ions to an aqueous solution of silver nitrate. The light yellow to green-yeUow precipitate is less soluble in ammonia than silver chloride, but it easily dissolves in the presence of other complexing agents, such as thiosulfate ions. 

Silver Chloride. Silver chloride, AgCl, is a white precipitate that forms when chloride ion is added to a silver nitrate solution. The order of solubility of the three silver halides is Cl" > Br" > I. Because of the formation of complexes, silver chloride is soluble in solutions containing excess chloride and in solutions of cyanide, thiosulfate, and ammonia. Silver chloride is insoluble in nitric and dilute sulfuric acid. Treatment with concentrated sulfuric acid gives silver sulfate. 

Qualitative. The classic method for the quaUtative determination of silver ia solution is precipitation as silver chloride with dilute nitric acid and chloride ion. The silver chloride can be differentiated from lead or mercurous chlorides, which also may precipitate, by the fact that lead chloride is soluble ia hot water but not ia ammonium hydroxide, whereas mercurous chloride turns black ia ammonium hydroxide. Silver chloride dissolves ia ammonium hydroxide because of the formation of soluble silver—ammonia complexes. A number of selective spot tests (24) iaclude reactions with /)-dimethy1amino-henz1idenerhodanine, ceric ammonium nitrate, or bromopyrogaHol red [16574-43-9]. Silver is detected by x-ray fluorescence and arc-emission spectrometry. Two sensitive arc-emission lines for silver occur at 328.1 and 338.3 nm. 

Medicinal Preparations. Silver nitrate is used in medicine in the form of a stick, usually containing 1—3% silver chloride, or in solutions of varying concentrations. Uses of silver in medicine as of the 1990s are much reduced from earlier in the twentieth century because of the availabiHty of a... 

Other Uses. Photochromic glass contains silver chloride (80) and silver molybdate [13765-74-7] (81) (see Chromogenic materials). An apparatus coated with silver nitrate has been described for the detection of rain or snow (82). Treatment with silver-thiosulfate complex has been reported as dramatically increasing the post-harvest life of cut carnations (83). Silver sulfate has been used in the electrolytic coloring of aluminum (84). Silver sulfate also imparts a yellowish red color to glass bulbs (85). 

It has been prepared synthetically by Ewins in the following manner Meta-oxybenzoic acid is converted with the aid of dimethyl sulphate into m-methoxybenzoic acid, which is then nitrated, and from the nitration products 2-nitro-3-methoxybenzoic acid is separated. This is reduced to 2-amino-3-methoxybenzoic acid which on heating with methyl iodide, yields 2-methylamino-3-methoxybenzoic acid. On warming this with freshly precipitated silver chloride it yields damascenine hydrochloride. 

Iron(III) nitrate is soluble, but silver chloride is not When these two solutions are mixed, silver chloride precipitates. 

In Experiment 8 you determined the number of moles of silver chloride formed in the reaction of some sodium chloride with a known amount of silver nitrate. How many moles of sodium chloride reacted with the silver nitrate Compare this with the number of moles of sodium chloride you added. 

For example, sodium chloride continues to dissolve in water at 20°C until the concentration is about six moles per liter. The solubility of NaCl in water is 6 M at 20°C. In contrast, only a minute amount of sodium chloride dissolves in ethyl alcohol at 20°C. This solubility is 0.009 M. Even in a single liquid, solubilities differ over wide limits. The solids calcium chloride, CaCl2, and silver nitrate, AgNOa, have solubilities in water exceeding one mole per liter. The solid called silver chloride, AgCl, has a solubility in water of only 10 5 mole per liter. 

Though both silver nitrate and sodium chloride have high solubility in water, silver chloride is very slightly soluble. What will happen if we mix a solution of silver nitrate and sodium chloride Then, we will have a solution that includes the species present in a solution of silver chloride, Ag+(aq) and Cl (ag), but now they are present at high concentration The Ag+(agJ came from reaction (8) and the Cl (aq) came from reaction (6) and their concentrations far exceed the solubility of silver chloride. The result is that solid will be formed. The formation of solid from a solution is called precipitation ... 

When we study a solid that does not have the characteristic lustrous appearance of a metal, we find that the conductivity is extremely low. This includes the solids we have called ionic solids sodium chloride, sodium nitrate, silver nitrate, and silver chloride. It includes, as well, the molecular crystals, such as ice. This solid, shown in Figure 5-3, is made up of molecules (such as exist in the gas phase) regularly packed in an orderly array. These poor conductors differ widely from the metals in almost every property. Thus electrical conductivity furnishes the key to one of the most fundamental classification schemes for substances. 

We have seen in Experiment 8 that silver chloride has low solubility in water. This is also true for silver bromide and silver iodide. In fact, these low solubilities provide a sensitive test for the presence of chloride ions, bromide ions, and iodide ions in aqueous solutions. If silver nitrate... 

The solubility of silver chloride is so low that all but a negligible amount of it is precipitated when excess sodium chloride solution is added to silver nitrate solution. What would be the weight of the precipitate formed when 100 ml of 0.5 M NaCl is added to 50.0 ml of 0.100 M AgNOs ... 

The theory of the process is as follows. This is a case of fractional precipitation (Section 2.8), the two sparingly soluble salts being silver chloride (Xsol 1.2 x 10 10) and silver chromate (Kso] 1.7 x 10 12). It is best studied by considering an actual example encountered in practice, viz. the titration of, say, 0.1M sodium chloride with 0.1M silver nitrate in the presence of a few millilitres of dilute potassium chromate solution. Silver chloride is the less soluble salt and the initial chloride concentration is high hence silver chloride will be precipitated. At the first point where red silver chromate is just precipitated both salts will be in equilibrium with the solution. Hence ... 

Procedure. Pipette 25 mL of the standard OAM sodium chloride into a 250 mL conical flask. Add 10 drops of either fluorescein or dichlorofluorescein indicator, and titrate with the silver nitrate solution in a diffuse light, while rotating the flask constantly. As the end point is approached, the silver chloride coagulates appreciably, and the local development of a pink colour upon the addition of a drop of the silver nitrate solution becomes more and more pronounced. Continue the addition of the silver nitrate solution until the precipitate suddenly assumes a pronounced pink or red colour. Repeat the titration with two other 25 mL portions of the chloride solution. Individual titrations should agree within 0.1 mL. 

Discussion. The chloride solution is treated with excess of standard silver nitrate solution, and the residual silver nitrate determined by titration with standard thiocyanate solution. Now silver chloride is more soluble than silver thiocyanate, and would react with the thiocyanate thus ... 

Determination of chloride as silver chloride Discussion. The aqueous solution of the chloride is acidified with dilute nitric acid in order to prevent the precipitation of other silver salts, such as the phosphate and carbonate, which might form in neutral solution, and also to produce a more readily filterable precipitate. A slight excess of silver nitrate solution is added, whereupon silver chloride is precipitated ... 

The supporting electrolyte may be 0.5 M potassium nitrate for bromide and iodide for chloride, 0.5 M potassium nitrate in 25-50 per cent ethanol must be used because of the appreciable solubility of silver chloride in water. 

This electrode is perhaps next in importance to the calomel electrode as a reference electrode. It consists of a silver wire or a silver-plated platinum wire, coated electrolytically with a thin layer of silver chloride, dipping into a potassium chloride solution of known concentration which is saturated with silver chloride this is achieved by the addition of two or three drops of 0.1M silver nitrate solution. Saturated potassium chloride solution is most commonly employed in the electrode, but 1M or 0.1 M solutions can equally well be used as explained in Section 15.1, the potential of the electrode is governed by the activity of the chloride ions in the potassium chloride solution. 

Prepare an approximately 0.1 M silver nitrate solution. Place 0.1169 g of dry sodium chloride in the beaker, add 100 mL of water, and stir until dissolved. Use a silver wire electrode (or a silver-plated platinum wire), and a silver-silver chloride or a saturated calomel reference electrode separated from the solution by a potassium nitrate-agar bridge (see below). Titrate the sodium chloride solution with the silver nitrate solution following the general procedure described in Experiment 1 it is important to have efficient stirring and to wait long enough after each addition of titrant for the e.m.f. to become steady. Continue the titration 5 mL beyond the end point. Determine the end point and thence the molarity of the silver nitrate solution. 

Instead of using an indicator, an ion-sensitive electrode can be used. An aqueous solution is titrated potentiometrically against 0.04 N hyamine 1622 solution using a nitrate ion-selective electrode and a silver/silver chloride reference electrode [106]. 

Some ionic compounds are soluble, others are not. Consider what happens when we pour a solution of sodium chloride (a strong electrolyte) into a solution of silver nitrate (another strong electrolyte). A solution of sodium chloride contains Na+ cations and Cl anions. Similarly, a solution of silver nitrate, AgNO, contains Ag+ cations and NO, anions. When we mix these two aqueous solutions, a white precipitate, a cloudy, finely divided solid deposit, forms immediately. Analysis shows that the precipitate is silver chloride, AgCl, an insoluble white solid. The... 

FIGURE 1.5 (a) Silver chloride precipitates immediately when sodium chloride solution is added to a solution of silver nitrate, (b) If we imagine the removal of the spectator ions from the complete ionic reaction (top), we can focus on the essential process, the net ionic reaction (bottom). 

Silver bromide Silver chloride Silver perchlorate Silver cyanide Silver fluoride Silver iodide Silver permar>gate Silver nitrate Silver carbonate Silver oxide Silver sulphate Silver sulphide Silver phosphate... 

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