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A solution of tin(II) chloride containing a little hydrochloric acid is used for the tin-plating of steel, in order to make tin cans. An electric potential is applied, and tin metal is formed at the cathode via electrolysis. Tin(II) chloride is used as a mordant in textile dyeing because it gives brighter colours with some dyes e.g. cochineal ...
The tin(II) chloride reduces the chloroauric acid from the dissolution of gold in aqua regia to a colloid of elemental gold supported on tin dioxide to give a purple precipitate or coloration. When used as a test, the intensity of the color correlates with the concentration of gold present. This test was first observed and refined by a German ...
The next step is to add dilute stannous chloride reagent, which has been freshly prepared from concentrated stannous chloride reagent and distilled water, to the mixture in the tube. This will produce a blue colour (due to the formation of molybdenum blue ) and the depth of the blue colour indicates the amount of phosphate in the boiler water.
Tin(II) chloride (also known as stannous chloride) is the most important commercial tin halide. Illustrating the routes to such compounds, chlorine reacts with tin metal to give SnCl 4 whereas the reaction of hydrochloric acid and tin produces SnCl 2 and hydrogen gas.
Stannous compounds that contain the Sn 2+ ion, such as tin(II) chloride; Sulfur dioxide (sometimes also used as an oxidizing agent), Sulfite compounds; Dithionates, e.g. Na 2 S 2 O 6; Thiosulfates, e.g. Na 2 S 2 O 3 (mainly in analytical chemistry) [11] Iodides, such as potassium iodide (K I) (mainly in analytical chemistry) Hydrogen peroxide ...
Chlorides are confirmed by the chromyl chloride test. When the salt is heated with K 2 Cr 2 O 7 and concentrated H 2 SO 4, red vapours of chromyl chloride (CrO 2 Cl 2) are produced. Passing this gas through a solution of NaOH produces a yellow solution of Na 2 CrO 4. The acidified solution of Na 2 CrO 4 gives a yellow precipitate with the ...
Substitutes that increase the electron density promote the formation of the aldimine-tin chloride adduct. With electron withdrawing substituents, the formation of an amide chloride is facilitated. [4] In the past, the reaction was carried out by precipitating the aldimine-tin chloride, washing it with ether and then hydrolyzing it.
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