| 21. | Monomethyldiborane yield is best with a ratio of 4 of diborane to 1 of trimethylborane.
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| 22. | When methyllithium reacts with diborane, monomethyldiborane is produced in about a 20 % yield.
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| 23. | Ammonia borane finds some use in organic synthesis as an air-stable derivative of diborane.
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| 24. | Adding phosphine or arsine results in slower deposition, while adding diborane increases the deposition rate.
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| 25. | Oxidation of borane gives diborane ( 6 ), being the dominant species with increasing temperature.
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| 26. | The yield of trimethyldiborane is maximised with ratio of 1 of diborane to 3 of trimethylborane.
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| 27. | Methylboranes such as tetramethyldiborane disproportionate in the gas phase to trimethylborane and diborane at room temperature.
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| 28. | Diborane is a little bit lighter than air, but will explode spontaneously when mixed with air.
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| 29. | The bonding in the Fe-H-Fe subunit is described using concepts developed for diborane.
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| 30. | Reactions requiring borane as opposed to diborane ( 6 ), must be carried out in solution.
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