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The k' pathway implicates a reaction between the doubly charged anion (RCHO 2 2−) and the aldehyde. The direct transfer of hydride ion is evident from the observation that the recovered alcohol does not contain any deuterium attached to the α-carbon when the reaction is performed in the presence of D 2 O.
Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.
Hydroboration–oxidation reaction is a two-step hydration reaction that converts an alkene into an alcohol. [1] The process results in the syn addition of a hydrogen and a hydroxyl group where the double bond had been. Hydroboration–oxidation is an anti-Markovnikov reaction, with
The hydride reacts with the weak Bronsted acid releasing H 2. Hydrides such as calcium hydride are used as desiccants, i.e. drying agents, to remove trace water from organic solvents. The hydride reacts with water forming hydrogen and hydroxide salt. The dry solvent can then be distilled or vacuum transferred from the "solvent pot".
Reduction via the net transfer of hydrogen from one organic molecule to another is known as transfer hydrogenation. Transfer hydrogenation to ketones leads to alcohols (the Meerwein-Ponndorf-Verley reduction ), and in the presence of a chiral transition metal catalyst, this process may be rendered enantioselective.
The substrate is coordinated to the zinc and this enzyme has two zinc atoms per subunit. One is the active site, which is involved in catalysis. In the active site, the ligands are Cys-46, Cys-174, His-67, and one water molecule. The other subunit is involved with structure. In this mechanism, the hydride from the alcohol goes to NAD +. Crystal ...
Aluminium hydride reduces acetals to half protected diols. [1] Acetal reduction using aluminium hydride. Aluminium hydride reduces epoxide to the corresponding alcohol: [1] Epoxide reduction using aluminium hydride. The allylic rearrangement reaction carried out using aluminium hydride is a S N 2 reaction, and it is not sterically demanding: [1]
Potassium hydride is produced by direct combination of the metal and hydrogen at temperatures between 200 and 350 °C: 2 K + H 2 → 2 KH. This reaction was discovered by Humphry Davy soon after his 1807 discovery of potassium, when he noted that the metal would vaporize in a current of hydrogen when heated just below its boiling point. [4]: p.25