MgCO3 Increasing acidity will cause the following reaction Mg.pdf

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MgCO3: Increasing acidity will cause the following reaction: MgCO3(s) + 2H+ ==> Mg(2+) + H2O + CO2(g) and thus the solubility will increase. AgI: Increasing acidity will NOT affect the solubility. CuS: Increasing acidity will cause the following reaction: CuS(s) + 2H+ ==> Cu(2+) + H2S(g) and thus the solubility will increase. PbBr2: Increasing acidity will NOT affect the solubility. Ba(OH)2 The solubility of Ba(OH)2 in water is only 5.6 g/100 g. By acidifying the solution, the following reaction take place: H+ + OH- ==> H2O and thus [OH-] would drop, and thus Ba(OH)2 solubility would be increased. Solution MgCO3: Increasing acidity will cause the following reaction: MgCO3(s) + 2H+ ==> Mg(2+) + H2O + CO2(g) and thus the solubility will increase. AgI: Increasing acidity will NOT affect the solubility. CuS: Increasing acidity will cause the following reaction: CuS(s) + 2H+ ==> Cu(2+) + H2S(g) and thus the solubility will increase. PbBr2: Increasing acidity will NOT affect the solubility. Ba(OH)2 The solubility of Ba(OH)2 in water is only 5.6 g/100 g. By acidifying the solution, the following reaction take place: H+ + OH- ==> H2O and thus [OH-] would drop, and thus Ba(OH)2 solubility would be increased..

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and thus the solubility will increase.
PbBr2:
Increasing acidity will NOT affect the solubility.
Ba(OH)2
The solubility of Ba(OH)2 in water is only 5.6 g/100 g. By acidifying the solution, the following
reaction take place:
H+ + OH- ==> H2O
and thus [OH-] would drop, and thus Ba(OH)2 solubility would be increased.

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The water must be boiled to remove traces of dissolved carbon dioxide (CO2). CO2 dissolves in water to form carbonic acid (H2CO3): CO2 + H2O => H2CO3 H2CO3 is a weak acid and partially ionizes to give H+ ions: H2CO3 => H+ + HCO3- HCO3- => H+ + CO32- The H+ ions can decompose thiosulfate ions and reduce the concentration of sodium thiosulfate according to the reaction: 2 S2O32- + H+ => HSO3- + S Solution The water must be boiled to remove traces of dissolved carbon dioxide (CO2). CO2 dissolves in water to form carbonic acid (H2CO3): CO2 + H2O => H2CO3 H2CO3 is a weak acid and partially ionizes to give H+ ions: H2CO3 => H+ + HCO3- HCO3- => H+ + CO32- The H+ ions can decompose thiosulfate ions and reduce the concentration of sodium thiosulfate according to the reaction: 2 S2O32- + H+ => HSO3- + S.

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What property of proteins us used to separate them in HIC Hydrophobic interaction chromatography (HIC) isolates Proteins in light of their hydrophobicity, and is regularly utilized as a middle stride as a part of a cleaning plan. Proteins are bound to a stationary stage in a high ionic quality cushion and, along these lines, HIC can commonly be performed instantly after particle trade chromatography with no cradle trade or weakening required. HIC is likewise usually performed after an ammonium sulfate precipitation, a strategy that can be utilized to rapidly expel proteins by accelerating a few, yet not all, proteins with salt. HIC is infrequently material in early strides of a purging plan or as a last stride in the expulsion of follow polluting influences from the protein of intrigue. ==================================================== Described mobile and stationary phase in HIC Hydrophobic association chromatography (HIC) is an other option to turned around stage chromatography for abusing the hydrophobic properties of proteins. The expansion of a salt to the mobile stage support and test arrangement advances protein- medium connections. The proteins are adsorbed to the medium in a mobile stage containing a high grouping of salt. The vast majority of the bound proteins are viably desorbed by essentially washing with water or a weaken, close impartial support. Since HIC utilizes a more polar, less denaturing environment than RPLC, it is getting to be well known for protein filtration, regularly in blend with particle trade or gel filtration chromatography. Solution What property of proteins us used to separate them in HIC Hydrophobic interaction chromatography (HIC) isolates Proteins in light of their hydrophobicity, and is regularly utilized as a middle stride as a part of a cleaning plan. Proteins are bound to a stationary stage in a high ionic quality cushion and, along these lines, HIC can commonly be performed instantly after particle trade chromatography with no cradle trade or weakening required. HIC is likewise usually performed after an ammonium sulfate precipitation, a strategy that can be utilized to rapidly expel proteins by accelerating a few, yet not all, proteins with salt. HIC is infrequently material in early strides of a purging plan or as a last stride in the expulsion of follow polluting influences from the protein of intrigue. ==================================================== Described mobile and stationary phase in HIC Hydrophobic association chromatography (HIC) is an other option to turned around stage chromatography for abusing the hydrophobic properties of proteins. The expansion of a salt to the mobile stage support and test arrangement advances protein- medium connections. The proteins are adsorbed to the medium in a mobile stage containing a high grouping of salt. The vast majority of the bound proteins are viably desorbed by essentially washing with water or a weaken, close impartial support. Since HIC uti.

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