Mercury(II) sulfate

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Mercury(II) sulfate
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Names
Other names
Mercuric sulfate, Mercurypersulfate, Mercury Bisulfate[1]
Identifiers
7783-35-9 YesY
PubChem 24544
Properties
HgSO4
Molar mass 296.653 g/mol
Appearance white monoclinic crystals
Odor odorless
Density 6.47 g/cm³, solid
450 °C Decomposes[2]
Decomposes in water to yellow mercuric subsulfate and sulfuric acid[3]
Solubility soluble in hot H2SO4, NaCl solution
insoluble in alcohol, acetone, ammonia
Structure
rhombic
Thermochemistry
−707.5 kJ mol−1[4]
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Mercury(II) sulfate, commonly called mercuric sulfate, is the chemical compound HgSO4. It is an odorless solid that forms white granules or crystalline powder. In water, it separates into an insoluble sulfate with a yellow color and sulfuric acid.[4]

History

In 1932, the Japanese chemical company Chisso Corporation began using mercury sulfate as the catalyst for the production of acetaldehyde from acetylene and water. Though it was unknown at the time, methylmercury is formed as side product of this reaction. Exposure and consumption of the mercury waste products, including methylmercury, that were dumped into Minamata Bay by Chisso are believed to be the cause of Minamata disease in Minamata, Japan.[5]

Production

Mercury sulfate, HgSO4, can be produced By heating concentrated H2SO4 with elemental mercury:[6]

Hg + 2 H2SO4 → HgSO4 + SO2 + 2 H2O

Or by dissolving solid yellow mercuric oxide in concentrated sulfuric acid and water. [7]

Uses

Denigés' reagent

An acidic solution of mercury sulfate is known as Denigés' reagent. It was commonly used throughout the 20th century as a qualitative analysis reagent. If Denigés' reagent is added to a solution containing compounds that have tertiary alcohols, a yellow or red precipitate will form.[8]

Production of Acetaldehyde

As previously mentioned, HgSO4 was used as the catalyst for the production of acetaldehyde from acetylene and water.[9]

The use of HgSO4 as a catalyst in the production of Acetaldehyde

Oxymercuration-Demercuration of Alkenes

Mercury Compounds such as mercury sulfate and mercury(II) acetate are commonly used as catalysts in the oxymercuration-demercuration, a type of Electrophilic Addition reactions. The hydration of an alkene results in an alcohol that follows regioselectivity that is predicted by Markovnikov's Rule[citation needed].

Hydration of Alkynes

The reaction scheme is provided below. The conversion of 2,5-dimethyhexyn-2,5-diol to 2,2,5,5-tetramethylte-trahydrofuran using aqueous mercury sulfate without the addition of acid.[10]

Conversion of 2,5-dimethyhexyn-2,5-diol to 2,2,5,5-tetramethylte-trahydrofuran-3-one

Health Issues

Inhalation of HgSO4 can result in acute poisoning: causing tightness in the chest, difficulties breathing, coughing and pain. Exposure of HgSO4 to the eyes can cause ulceration of conjunctiva and cornea. If mercury sulfate is exposed to the skin it may cause sensitization dermatitis. Lastly, ingestion of mercury sulfate will cause necrosis, pain, vomiting, and severe purging. Ingestion can result in death within a few hours due to peripheral vascular collapse.[1]

It has, however, been successfully used in the late 19th century to induce vomiting for medical reasons. [1]

References

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  3. chembook
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  5. http://www.hgtech.com/Information/Minamata_Japan.html
  6. http://www.epa.gov/hg/pdfs/mercury-rpt-to-congress.pdf
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External links