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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 is the mechanism by which hydraulic binders such as Portland cement develop strength. A hydraulic binder is a material that can set and harden submerged in water by forming insoluble products in a hydration reaction. The term hydraulicity or hydraulic activity is indicative of the chemical affinity of the hydration reaction. [2]
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
The reaction thus provides a more stereospecific and complementary regiochemical alternative to other hydration reactions such as acid-catalyzed addition and the oxymercuration–reduction process. The reaction was first reported by Herbert C. Brown in the late 1950s [2] and it was recognized in his receiving the Nobel Prize in Chemistry in 1979.
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.
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 ...
If the hydration energy is greater than the lattice energy, then the enthalpy of solution is negative (heat is released), otherwise it is positive (heat is absorbed). [3]The hydration energy should not be confused with solvation energy, which is the change in Gibbs free energy (not enthalpy) as solute in the gaseous state is dissolved. [4]
The classic example of a dehydration reaction is the Fischer esterification, which involves treating a carboxylic acid with an alcohol to give an ester RCO 2 H + R′OH ⇌ RCO 2 R′ + H 2 O. Often such reactions require the presence of a dehydrating agent, i.e. a substance that reacts with water.