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Experiments for 'hydrogen peroxide'
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Results for 'hydrogen peroxide':
EXPERIMENT 1 --------------- Nitrous vapors react with thiocyanate, building a red/brown compound, which disappears again, when left in contact with air.
EXPERIMENT 2 --------------- Thiocyanate reacts with nitrogen dioxide to form a red/brown compound. It does not react with nitrogen monoxide. When a reaction occurs with NO2, a white fume is produced.
EXPERIMENT 3 --------------- Vanadium(III) hydroxide apparently forms a precipitate and does not dissolve in strongly alkaline liquids. Vanadium (III) and (IV) are oxidized by peroxodisulfate to vanadium (V).
EXPERIMENT 4 --------------- Hydrogen peroxide builds complexes with vanadium (IV) and vanadium (V) species. These compounds are not stable and result in dissociation of the complex and formation of vanadium (IV) compounds. The net result of adding hydrogen peroxide to a solution containing vanadium (V) can be reduction to vanadium (IV) with the formation of oxygen.
EXPERIMENT 5 --------------- Vanadium (III) apparently builds a coordination complex with EDTA in strongly acidic environments. This complex is brown.
EXPERIMENT 6 --------------- Vanadyl builds an intensely colored complex with thiocyanate in acidic environments. In alkaline environments this complex is destroyed. When H2O2 is added, this complex is destroyed as well, but in this case some heating is required.
EXPERIMENT 7 --------------- Vanadium (IV) does not readily yield precipitates with alkaline compounds. Carbonate is not capable of precipitating this. Hydrogen peroxide builds a complex with vanadium (V) and possibly with vanadium (IV). Diverse coloured compounds are formed in sequence. What is their constitution?
EXPERIMENT 8 --------------- Vanadyl ions do not form a special complex with tartaric acid in strongly acidic environments. When hydrogen peroxide is added, a complex is formed, but is this due to the presence of tartaric acid? When tartaric acid is added to a solution of vanadyl sulfate in an environment, which is only slightly acidic, then a green complex is formed. On making the liquid more basic, a vague sequence of color changes occurs, through grey/blue, finally going to brown.
EXPERIMENT 9 --------------- Vanadium (V) compounds form yellow compouds with hydrogen peroxide in alkaline environments, with strong solutions and very high alkalinity grey and blue compounds are formed, which, however, decompose easily.
EXPERIMENT 10 --------------- Vanadium (V) is capable of forming many peroxo compounds, whose appearance strongly depends on pH.
EXPERIMENT 11 --------------- Without the help of a strong acid, vanadium pentoxide is not capable of oxidizing formic acid, not even when heated. When some sulfite is added, then incomplete reduction of the V2O5 can be observed. With the help of a strong acid and when in solution, vanadium (V) is capable of oxidizing formic acid, but only very slowly. With formic acid and vanadium (IV), apparently a coordination complex is formed. Another explanation is given below at the end of the description.
EXPERIMENT 12 --------------- Vanadium in its +4 oxidation state forms a blue compound, vanadyl, in acidic environments. In near neutral to alkaline environments, the situation is less clear. Reduction of neutral or alkaline vanadium (V) compounds yields a dark and turbid liquid. Vanadium in its +5 oxidation state gives light yellow compounds in mildly alkaline environments. Al lowering the pH, the color becomes more intense, until a maximum is reached. When the pH is lowered even more, then lighter yellow compounds are formed again. Vanadium (IV) cannot coexist with hydrogen peroxide. In alkaline media it is oxidized to vanadium (V), which with excess peroxide gives a yellow peroxo complex. In acidic media, vanadium (IV) is oxidized to vanadium (V) which gives a deep brown/red peroxo complex with excess poroxide.
EXPERIMENT 13 --------------- Copper (II) reacts with thiocyanate in a complex way.
EXPERIMENT 14 --------------- Copper is oxidized by a mix of concentrated hydrochloric acid and hydrogen peroxide. When the peroxide is used up and there is still an excess amount of hydrochloric acid, then the copper (II) appears to oxidize the copper metal, under the formation of an intensely colored complex. (What is the constitution of this complex??) When the solution is diluted with water, then the intensely colored complex is destroyed and a white crystalline precipitate of CuCl is formed. If too much water is used, then no clear precipitate is formed.
EXPERIMENT 15 --------------- Copper (II) reacts with metallic copper, in the presence of a large amount of hydrochloric acid, forming an intensely colored compound. This compound contains copper (I). If copper (II) is used alone, with hydrochloric acid and peroxide, then the strong coloration does not occur.
EXPERIMENT 16 --------------- Hydroquinone is capable of reducing copper (II) to copper (I) in alkaline environments. The copper is not reduced to its metallic form.
EXPERIMENT 17 --------------- Copper builds higher oxides than CuO when strong oxidizing agents are present in alkaline environments. Probably these are not copper (III) compounds, but the oxo-ion probably is replaced by peroxo or superoxo.
EXPERIMENT 18 --------------- Decomposition of hydrogen peroxide is catalyzed by cuprammine complex.
EXPERIMENT 19 --------------- In alkaline environments, copper (II) shows remarkable behavior, when brought in contact with strong oxidizers or reductors.
EXPERIMENT 20 --------------- Copper builds a remarkable complex with ascorbic acid and is easily reduced by ascorbic acid in alkaline environments. Copper (II) builds a brown compound with hydrogen peroxide in alkaline environments.
EXPERIMENT 21 --------------- Copper and nickel carbonates (basic), which do not dissolve in water, do dissolve in ammonia, due to formation of a complex with ammonia. Cobalt carbonate also dissolves, but now an additional reaction occurs, taking up oxygen from the air.
EXPERIMENT 22 --------------- Copper (II) builds a coordination complex with acetate ions. On addition of hydrogen peroxide, this complex is destroyed and a new compound is formed.
EXPERIMENT 23 --------------- Copper (II) amine complex is reduced to a colorless copper (I) amine complex by hydroxyl amine. The copper (I) complex is oxidized by oxygen from the air very easily.
EXPERIMENT 24 --------------- Copper (II) salts give a cyan precipitate with bicarbonates. The color of this precipitate is the same as the color of commercially available basic copper carbonate. This precipitate reacts with hydrogen peroxide, forming a dark green/brown compound. With sulfite it also reacts, forming a brownish compound, which on acidification dissolves, forming a light yellow/brown clear liquid.
EXPERIMENT 25 --------------- Copper (II) is reduced by metabisulfite / sulphur dioxide to a copper (I) compound, but some heating is required in order to make this reaction fast.
EXPERIMENT 26 --------------- When copper (II) is present in hydrochloric acid, then it does not react immediately with hydroxyl ammonium, some heating is required to have a reaction, resulting in formation of a dark green/brown compound. When the liquid is made alkaline with excess ammonia, then it quickly becomes colorless, due to reduction of copper (II) to copper (I), which forms a colorless complex with ammonia. A very peculiar reaction occurs on oxidation by oxygen from air. The liquid is covered by a very thin shiny layer, looking like a strongly coloured oil on water. It is not clear what it is, more research is needed.
EXPERIMENT 27 --------------- Copper (II) carbonate gives a very dark compound with H2O2, is this a peroxide compound or just copper oxide?
EXPERIMENT 28 --------------- Palladium (II) is not oxidized by H2O2 in acidic environments.
EXPERIMENT 29 --------------- Titanium slowly dissolves in concentrated hydrochloric acid, forming deep blue/violet titanium (III) ions. On addition of hydrogen peroxide these are oxidized to titanium (IV), which in turn forms a deep red coordination complex with hydrogen peroxide. The deep red coordination complex is only stable in acidic to neutral media. It also is easily reduced by nitrite. It is not affected strongly by persulfate. With fluoride, a light yellow compound is formed, but the formation of that may also be due to rise of pH.
EXPERIMENT 30 --------------- Zinc (II) gives a white precipitate with ferrocyanide. This precipitate becomes pale yellow, when treated with hydrogen peroxide (at least, when in acidic environment).
EXPERIMENT 31 --------------- Cobalt (II) appears to react with ammonia, but only when an oxidizer is available. The resulting compound has an intense color.
EXPERIMENT 32 --------------- Cobalt gives a green coordination complex with tartrates, when oxidized to the +3 state.
EXPERIMENT 33 --------------- Cobalt (II) gives a coordination complex with catechol (or is this due to formation of a cobalt (III) complex with catechol????).
EXPERIMENT 34 --------------- Cobalt (II) is stable in acidic environments, but in alkaline environments in the presence of ammonia it reacts with oxygen from the air, resulting in the formation of a dark red/brown coordination complex.
EXPERIMENT 35 --------------- Cobalt (II) gives a precipitate with bicarbonate, which reacts with hydrogen peroxide, probably forming a cobalt (III) compound.
EXPERIMENT 36 --------------- Cobalt forms many complexes with ammonia and it forms these complexes easily, but when cobaltosic oxide (Co3O4, black oxide) is used, then no such reactions can be observed. Co3O4 appears to be very inert.
EXPERIMENT 37 --------------- Cobalt (II) salts give a blue/green precipitate when dilute ammonia is added. This precpitate is fairly stable towards air. When more concentrated ammonia is used, then a dark brown compound is formed, but this compound is formed by contact with air. On addition of hydrogen peroxide also a very dark brown compound is formed. When the pH is increased strongly, then the blue precipitate is not stable anymore, instead a dark bright blue compound is formed, which, however, quickly turns pink. When a large amount of ammonia is replaced by ammonium, then the blue precipitate is not formed anymore, but a coordination complex is formed, which is very easily oxidized by oxygen from the air.
EXPERIMENT 38 --------------- Cobalt sulfide does not dissolve in dilute acids and it does not dissolve in concentrated hydrochloric acid (at least not easily). With the help of hydrogen peroxide it is possible, however, to dissolve the compound.
EXPERIMENT 39 --------------- Cobalt (II) gives a green precipitate with ferrocyanide and a dark red/ purple precipitate with ferricyanide. The green precipitate cannot be converted to the red one by means of oxidation by hydrogen peroxide, but another, dark blue, compound is formed.
EXPERIMENT 40 --------------- The hexanitrito cobaltate (III) ion can be reduced by SO2 to cobalt (II), but this reduction requires heating. Some brown compound remains, this probably is due to the inertness of many cobalt (III) coordination complexes. With nitrite, a brown complex is formed again. This differs from the gold/yellow hexanitrito cobaltate (III).
EXPERIMENT 41 --------------- The hexanitrito cobaltate (III) ion is affected by concentrated nitric acid. It changes from yellow to brown. What is the nature of this change?
EXPERIMENT 42 --------------- The hexanitrito cobaltate (III) ion is stable towards dilute sulphuric acid. Addition of hydrogen peroxide also does not destroy the yellow complex.
EXPERIMENT 43 --------------- In this experiment, some of Werner's experiments are repeated. Here it is shown that cobalt forms beautifully colored carbonato complexes. The exact complex formed, depends on the experimental conditions. It is remarkable what kinds of reactions are shown by cobalt in its complexes and it is really difficult to precisely determine what is happening and it even is difficult already to get the same results without precisely specifying the exact experimental conditions (e.g. using HCl instead of H2SO4 already results in a different outcome).
EXPERIMENT 44 --------------- Acetone can be mixed with water in any ratio, but when sodium hydroxide is added, then the liquids are not miscible in any ratio anymore. Sulphur reacts with acetone in the presence of sodium hydroxide. Sulfide does not show such a reaction.
EXPERIMENT 45 --------------- Sodium sulfide is oxidized by acidic hydrogen peroxide with extreme violence.
EXPERIMENT 46 --------------- When molybdates are reduced, then intense blue compounds are formed. It is believed that these intensely coloured compounds are multi-nuclear Mo-compounds, with different nuclei having different oxidation states.
EXPERIMENT 47 --------------- In strongly alkaline environments, molybdates are not as easily reduced as in neutral or acidic environments.
EXPERIMENT 48 --------------- Molybdate forms strongly colored, but unstable, complexes with hydrogen peroxide.
EXPERIMENT 49 --------------- Molybdate forms blue or green compounds, when reduced with mild reducing agents or when little quantitities of reducing agents are used.
EXPERIMENT 50 --------------- Molybdates and orthophosphates give a yellow complex, which is reduced more easily than molybdates alone.
EXPERIMENT 51 --------------- Hydroquinone is oxidized by hydrogen peroxide. This reaction is slow in a neutral environment.
EXPERIMENT 52 --------------- Ferric chloride enhances the oxidation of hydroquinone by hydrogen peroxide considerably. Besides this, a coordination complex appears to be formed when ferric chloride is added to an hydroquinone/peroxide solution.
EXPERIMENT 53 --------------- Diverse phenol-derivatives, can be oxidized easily by bromine, yielding intensely colored oxidation products.
EXPERIMENT 54 --------------- Hydroquinone is not oxidized to the dark brown product by hydrogen peroxide as it is done by oxygen from the air in alkaline environments.
EXPERIMENT 55 --------------- Photography developers, based on phenol-like structures, are easily oxidized by air in alkaline environments and the oxidation products are such, that a reverse process does not occur anymore (probably the oxidation products are large polymerized species).
EXPERIMENT 56 --------------- Phenidone is oxidized by air, but is much less susceptible to oxidation than developers, such as hydroquinone, pyrogallol.
EXPERIMENT 57 --------------- It appears that copper (II) ions catalyse the oxidation of pyrogallol by hydrogen peroxide.
EXPERIMENT 58 --------------- The coordination complexes formed by iron-salts and phenol-like photographic developers show very typical reactions with hydrogen peroxide. Many times these reactions result in oxidation products which are not dark colored, as opposed for oxidation by atmospheric oxygen.
EXPERIMENT 59 --------------- When p-aminophenol is oxidized in an acidic environment, then a compound is formed, with a deep indigo/purple color.
EXPERIMENT 60 --------------- When hydroquinone is oxidized by hydrogen peroxide in acidic environments, then a pale yellow compound is formed. This is in strong contrast with oxidation by oxygen from air in alkaline environment, where a dark brown/ black compound is formed.
EXPERIMENT 61 --------------- P-aminophenol, when oxidized, forms a deeply colored compound. The color of this compound is deep blue/purple, but the environment and the used oxidizer have some influence on the color of the liquid as a whole (other compounds may make the color less pure).
EXPERIMENT 62 --------------- Vanadium pentoxide catalyzes the oxidation of hydroquinone to quinone by hydrogen peroxide.
EXPERIMENT 63 --------------- Bromide is oxidized by hydrogen peroxide in acidic environments. Addition of nitric acid strongly enhances the reaction.
EXPERIMENT 64 --------------- Potassium bromate is capable of oxidizing hydrogen peroxide, itself being reduced to bromine.
EXPERIMENT 65 --------------- Selenium dissolves in a sulfide solution, forming a deep red/brown solution. Hydrogen peroxide is capable of oxidizing this solution.
EXPERIMENT 66 --------------- Rhenium is oxidized easily by nitric acid. The oxidation product is a color- less compound, soluble in water (according to literature it is perrhenic acid, HReO4). Perrhenic acid is not a really strong oxidizer. It can be reduced by zinc, but addition of sodium sulfite does not result in formation of the same compound. Hydrogen peroxide is capable of oxidizing back to perrhenic acid, but some light yellow compound remains. What is it?
EXPERIMENT 67 --------------- Chromium (III) can be converted to chromium (VI) in strongly alkaline environments.
EXPERIMENT 68 --------------- Oxidation of chromium (III) to chromium (VI).
EXPERIMENT 69 --------------- Chromium (III) can be oxidized to chromium (VI) by persulfate in alkaline environments.
EXPERIMENT 70 --------------- Chromium (III) does not quickly build a coordination complex with ammonia, such as is the case with copper (II) and nickel (II). Even in a slightly alkaline environment of dilute ammonia, chromium (III) can be oxidized to chromium (VI) by the action of hydrogen peroxide. Reduction, back to chromium (III) is not easily accomplished in alkaline environment.
EXPERIMENT 71 --------------- Bleach is capable of oxidizing chromium (III) to its hexavalent state, but this is not accomplished easily and completely.
EXPERIMENT 72 --------------- When chromium (III) is created by reduction from dichromate with acidified sulfite, then a green ion is formed. When acidified sulfite is added to violet chromium (III), then the ions remain violet. Apparently the way of creating chromium (III) determines its color (and hence to what it is coordinated).
EXPERIMENT 73 --------------- Chromium (III) builds a green coordination complex with metabisulfite, not with thiosulfate. When hydrogen peroxide is added, then the complex with metabisulfite is destroyed.
EXPERIMENT 74 --------------- Sodium dichromate dissolves in water very well, much better than potassium dichromate. When it is reduced, then it is hard to crystallize a chrome (III) salt or a mixed sodium chrome (III) salt.
EXPERIMENT 75 --------------- From ice cold strongly alkaline solutions of potassium chromate, one can create peroxochromate by adding hydrogen peroxide carefully.
EXPERIMENT 76 --------------- Chromium (III) gives coordination complexes of all kinds of colours, when formed from a redox reaction, starting with dichromate.
EXPERIMENT 77 --------------- When dichromate is brought in contact with peroxide, then after an initial transient, a green variation of chromium (III) is produced. This compound, however, slowly changes to a bluish/violet compound.
EXPERIMENT 78 --------------- When dichromate is reduced by means of adding hydrogen peroxide, then after the initial transient a green compound is formed, even when the acid in which the dichromate is dissolved is nitric acid (nitrate is supposed to not form a coordination complex with chromium (III)). Is this green compound a coordination complex with nitrate? or with hydrogen peroxide? This coordination complex can easily be destroyed by heating.
EXPERIMENT 79 --------------- Chromium (III) builds a nice brightly colored green complex with phosphates. This compound has no bluish hue, like sulfate gives with chromium (III). Chloride also builds a complex. Formation of these complexes is not on simple addition of a chromium (III) salt to the corresponding anions. Heating is required.
EXPERIMENT 80 --------------- Dichromate reacts with hydrogen peroxide, also when no acid is present. An initial compound is formed quickly, which decomposes slowly, releasing heat. Due to heating up, the reaction proceeds faster and faster, until all of the peroxide has been used up.
EXPERIMENT 81 --------------- Chromic acid reacts with hydrogen peroxide under formation of a dark blue compound. When more hydrogen peroxide is added, then apparently the pH of the liquid becomes too high and other almost black compounds are formed, which quickly decompose.
EXPERIMENT 82 --------------- Dichromate reacts with hydrogen peroxide, yielding chromium (III) as the final product, in acidic environments. In alkaline environments, chromium (III) yields chromate with hydrogen peroxide.
EXPERIMENT 83 --------------- Aniline gives colored compounds with chromium. The colors are remarkably intense.
EXPERIMENT 84 --------------- Manganese (II) ions apparently do not form coordination complexes with EDTA. If they do so, then the coordination complex is (almost) colorless.
EXPERIMENT 85 --------------- Manganese (II) forms a white precipitate with bicarbonate, while slowly developing a gas (probably this is CO2). This precipitate is not quickly oxidized by oxygen from the air. When the precipitate is made more alkaline by adding hydroxide, then it is oxidized fairly quickly. Addition of hydrogen peroxide causes immediate oxidation of the alkaline precipitate.
EXPERIMENT 86 --------------- Sulfide is capable of forming a brightly coloured compound with antimony (III) in a strongly acidic environment. The sulfide is not destroyed by strong acid and is not converted to hydrogen sulfide gas.
EXPERIMENT 87 --------------- Dichromate is quickly reduced by tin (II) ions. Hydrogen peroxide does not show a visible reaction with tin (II) ions.
EXPERIMENT 88 --------------- Silver (I) gives a precipitate with bicarbonate, which becomes yellow and more compact on standing. With H2O2 a dark compound is formed, which dissolves in nitric acid under formation of a gas. Is this dark compound a higher oxide of silver (e.g. Ag2O2?).
EXPERIMENT 89 --------------- Silver (I) ions, when treated with hydroxide give brown silver (I) oxide. When hydrogen peroxide is added, then that is decomposed and the precipitate of oxide does not change noticeably. When, however, hydrogen peroxide is first mixed with a solution of a silver (I) salt and then the hydroxide is added, then a black precipitate is formed. Probably this is finely divided metallic silver.
EXPERIMENT 90 --------------- Acetone reacts with sulphur in strongly alkaline environments. What products are formed? A similar reaction is observed between methyl ethyl ketone and sulphur.
EXPERIMENT 91 --------------- Lead hydroxide is oxidized by hydrogen peroxide. The resulting compound does not dissolve in dilute nitric acid.
EXPERIMENT 92 --------------- Thiosulfate gives a purple coordination complex with iron (III). This complex, however, is not stable. With iron (II) no complex is formed. Iron (III) is reduced by thiosulfate after the initial formation of the purple coordination complex. This is shown by adding ferrocyanide, which does not result in formation of an intense dark blue precipitate.
EXPERIMENT 93 --------------- Ferricyanide gives a dark brown coordination complex with ferric ions. This complex is soluble in water. It is easily transformed to the much more stable, dark blue and insoluble ferroferricyanide.
EXPERIMENT 94 --------------- The experiment described below suggests the formation of a coordination complex between iron and ascorbate. The presence of the ascorbate induces a completely different behavior of ferric/ferrous ions in alkaline environments.
EXPERIMENT 95 --------------- Ferric ions apparently form a coordination complex with glucose in alkaline environments. Normally ferric ions give a brown precipitate in strong alkaline liquids, with glucose the liquid remains clear.
EXPERIMENT 96 --------------- Aluminium (III) does not form colored compounds with ferrocyanide nor with ferricyanide. Manganese (II) reacts with both of them, but a colored compound is formed with ferricyanide only.
EXPERIMENT 97 --------------- Ferrous sulfate is hard to dissolve cleanly in water. It usually is contaminated with some oxidation products and in the water it is slowly oxidized by air as well.
EXPERIMENT 98 --------------- Ferrocyanide and ferricyanide decompose on heating with dilute sulphuric acid. When the decomposition product of ferrocyanide is treated with hydrogen peroxide, then it looks very much like the decomposition product of ferricyanide.
EXPERIMENT 99 --------------- Ferrocyanide can be oxidized by hydrogen peroxide easily. This redox reaction makes the liquid alkaline: H2O2 + 2e --> 2OH-
EXPERIMENT 100 --------------- Ferrocyanide reacts with hydrogen peroxide, forming a fairly intensely colored yellow compound (probably ferricyanide), but this reaction was expected to make the liquid more alkaline, but this cannot be observed.
EXPERIMENT 101 --------------- Ferrocyanide in acidic environments reacts with bromine in a very peculiar way. An extremely dark compound is formed. This reaction does not occur in neutral environments and this cannot be observed with ferricyanides. What is the dark compound? Is it a coordination complex or a condensation product of many ferric/ferrous ions, close to formation of solid particles?
EXPERIMENT 102 --------------- Ferrous ions react with hydroxide, forming a light bluish/grey precipitate. This precipitate, however, quickly turns brown.
EXPERIMENT 103 --------------- Ferrous ions react with H2O2. At low pH, the H2O2 oxidizes the ferrous ions to ferric ions. At near neutral pH, a complex reaction occurs, the ferrous ions are converted to some complex with the H2O2. Ferric ions do not react with H2O2.
EXPERIMENT 104 --------------- Hydrogen peroxide probably serves as a reductor for an higher oxide of nickel.
EXPERIMENT 105 --------------- Catechol appears to react with nickel (II), giving a coordination complex. It is unclear, whether this is due to catechol itself or due to an oxidation product, caused by oxidation by oxygen from air.
EXPERIMENT 106 --------------- Nickel in nickel (II) hydroxide is oxidized to a higher oxidation state by hypochlorites, but not by chlorates. The oxidation product is reduced by hydrogen peroxide and ammonia. Heating of the oxidation product makes it more resistant to reduction and to breakdown by acids.
EXPERIMENT 107 --------------- Titanium metal slowly dissolves in concentrated hydrochloric acid and then forms a very dark solution of a titanium/chloride complex. This solution is much darker than an aqueous solution of titanium(III) in which the ions are present as aqua complex. With thiocyanate an even more intensely colored complex is formed. This complex has the same color, but it is very dark.
EXPERIMENT 108 --------------- Thiourea is oxidized in acidic solution to formamidine disulfide, which exists in solution as an acid salt. When a strong base is added, then the free base is formed, but this at once decomposes. One of the decomposition products is sulphur. When excess oxidizer is used and the pH is increased strongly, then the sulphur dissolves, giving rise to formation of polysulfides.
EXPERIMENT 109 --------------- Perchloric acid is very reluctant to reacting with many chemicals. This is different from what many sites are telling. Perchloric acid only is extremely reactive when it is anhydrous, the hydrous acid (60 ... 70%) is not that reactive.
EXPERIMENT 110 --------------- Chromium(III) oxide is extremely inert when it is calcined. It does not dissolve in the common acids, nor in solutions of common bases. The solid, however, can be oxidized by a solution of a bromate.
EXPERIMENT 111 --------------- Both oxone, active ion is HSO5(-), and peroxodisulfate, active ion is S2O8(2-), produce a black precipitate when added to nickel(II) ions at high pH. Hydrogen peroxide, on the other hand, only produces green nickel(II) hydroxide, and if the black precipitate is present, it is destroyed by hydrogen peroxide, with formation of oxygen and green nickel(II) hydroxide.
EXPERIMENT 112 --------------- When a solution of copper sulfate is added to a solution of hydroxyl ammonium chloride in dilute solution of NaOH, then a dirty green precipitate is formed. At some places the precipitate becomes yellow. When the liquid is shaken, then all of the precipitate dissolves and a colorless liquid is obtained. On standing, a thin layer of solid material is formed on the surface of the liquid. This layer has a dirty green color.
Hydroxyl amine reduces copper(II) at high pH and a colorless complex of copper(I) is formed, which at really high pH becomes unstable with formation of hydrous copper(I) oxide.
End of results for 'hydrogen peroxide'
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