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Hydration reaction mechanism from 1-methylcyclohexene to 1-methylcyclohexanol. Many alternative routes are available for producing alcohols, including the hydroboration–oxidation reaction , the oxymercuration–reduction reaction , the Mukaiyama hydration , the reduction of ketones and aldehydes and as a biological method fermentation .
Hydration reaction, a chemical addition reaction where a hydroxyl group and proton are added to a compound; Hydration shell, a type of solvation shell; Hydration system, an apparatus that helps its user drink enough liquid while engaged in physical activity Hydration pack, a type of hydration system composed of a carry-on pack used for hydration
Application of mukaiyama hydration in the total synthesis of (±)-Garsubellin A. The hydration reaction is catalyzed by Co(acac)2 (acac = 2,4-pentanedionato, better known as acetylacetonato) and carried out in the presence of air oxygen & phenylsilane. With isopropanol used as solvent, yields of 73 % are obtained.
The analysis of the possible pathways for this reaction has been cited as an example of the importance of considering activation energy of each mechanistic step. [2] The hydration of the carbonyl of ketene, which formally involves an addition reaction of one water molecule onto the carbonyl group, is likely catalyzed by a second water molecule. [3]
As it hydrates, an exothermic reaction results and the solid puffs up. The hydrate can be reconverted to quicklime by removing the water by heating it to redness to reverse the hydration reaction. One litre of water combines with approximately 3.1 kilograms (6.8 lb) of quicklime to give calcium hydroxide plus 3.54 MJ of energy.
This reaction is considered Markovnikov because the halogen substituent attaches to the more substituted carbon. Hydration: Can occur either in syn or anti addition fashion, depending on the solution it is in; 50% of each orientation. This reaction is considered Markovnikov because the hydroxyl group attaches to the more substituted carbon.
Mercury sulfate, as well as other mercury(II) compounds, are commonly used as catalysts in oxymercuration-demercuration, a type of electrophilic addition reaction that results in hydration of an unsaturated compound. The hydration of an alkene gives an alcohol. The regioselectivity is that predicted by Markovnikov's rule.
In organic chemistry, a hydrate is a compound formed by the hydration, i.e. "Addition of water or of the elements of water (i.e. H and OH) to a molecular entity". [5] For example: ethanol , CH 3 −CH 2 −OH , is the product of the hydration reaction of ethene , CH 2 =CH 2 , formed by the addition of H to one C and OH to the other C, and so ...