| 11. | The reduction of Si 2 Cl 6 with lithium aluminium hydride affords disilane in modest yield.
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| 12. | Especially for fine chemical syntheses, lithium aluminium hydride is used to reduce esters to two primary alcohols.
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| 13. | However, with lithium aluminium hydride it can simply be reduced to directly form amphetamine in moderate yields.
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| 14. | Molecular copper hydride can be formed by reducing copper iodide with lithium aluminium hydride in ether and pyridine.
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| 15. | Particularly common are sodium borohydride ( NaBH 4 ) and lithium aluminium hydride and hindered reagents such as DIBAL.
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| 16. | Similar to lithium aluminium hydride, it is a salt consisting of separated sodium cations and tetrahedral AlH anions.
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| 17. | They are the final precursor, reduced with lithium aluminium hydride to the final product ( an amine ).
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| 18. | Acyl chlorides are reduced by strong hydride donors such as lithium aluminium hydride and diisobutylaluminium hydride to give primary alcohols.
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| 19. | Carboxylic acid can be reduced to the alcohol by hydrogenation or using stoichiometric hydride reducing agents such as lithium aluminium hydride.
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| 20. | 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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