| 1. | Lithium aluminium hydride also reduces alkyl halides to alkanes,.
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| 2. | Lithium aluminium hydride does not reduce simple alkenes or arenes.
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| 3. | Quantitative analysis of hydroperoxides is performed using potentiometric titration with lithium aluminium hydride.
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| 4. | The hydride is lithium aluminium hydride and the leaving group a phosphonium salt.
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| 5. | The reaction with lithium aluminium hydride ( LAH ) results in an explosion.
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| 6. | LiBHEt 3 is far more reducing than lithium borohydride and lithium aluminium hydride.
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| 7. | Lithium methylborohydride can be made by reacting a methylboronic ester with lithium aluminium hydride.
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| 8. | Lithium aluminium hydride ( ) is commonly used as a reducing agent in organic synthesis.
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| 9. | Azoalkanes may be reduced to primary amines by the Staudinger reduction or lithium aluminium hydride.
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| 10. | Leading candidates are lithium hydride, sodium borohydride, lithium aluminium hydride and ammonia borane.
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