lithium aluminium hydride वाक्य
उदाहरण वाक्य
मोबाइल
- Lithium aluminium hydride also reduces alkyl halides to alkanes,.
- Lithium aluminium hydride does not reduce simple alkenes or arenes.
- Quantitative analysis of hydroperoxides is performed using potentiometric titration with lithium aluminium hydride.
- The hydride is lithium aluminium hydride and the leaving group a phosphonium salt.
- The reaction with lithium aluminium hydride ( LAH ) results in an explosion.
- LiBHEt 3 is far more reducing than lithium borohydride and lithium aluminium hydride.
- Lithium methylborohydride can be made by reacting a methylboronic ester with lithium aluminium hydride.
- Lithium aluminium hydride ( ) is commonly used as a reducing agent in organic synthesis.
- Azoalkanes may be reduced to primary amines by the Staudinger reduction or lithium aluminium hydride.
- Leading candidates are lithium hydride, sodium borohydride, lithium aluminium hydride and ammonia borane.
- The reduction of Si 2 Cl 6 with lithium aluminium hydride affords disilane in modest yield.
- Especially for fine chemical syntheses, lithium aluminium hydride is used to reduce esters to two primary alcohols.
- However, with lithium aluminium hydride it can simply be reduced to directly form amphetamine in moderate yields.
- Molecular copper hydride can be formed by reducing copper iodide with lithium aluminium hydride in ether and pyridine.
- Particularly common are sodium borohydride ( NaBH 4 ) and lithium aluminium hydride and hindered reagents such as DIBAL.
- Similar to lithium aluminium hydride, it is a salt consisting of separated sodium cations and tetrahedral AlH anions.
- They are the final precursor, reduced with lithium aluminium hydride to the final product ( an amine ).
- Acyl chlorides are reduced by strong hydride donors such as lithium aluminium hydride and diisobutylaluminium hydride to give primary alcohols.
- Carboxylic acid can be reduced to the alcohol by hydrogenation or using stoichiometric hydride reducing agents such as lithium aluminium hydride.
- With other reducing agents such as sodium borohydride or lithium aluminium hydride, the unstable and very toxic gas stibine is produced.
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