| 21. | In a related reaction, alkyl halides undergo nucleophilic displacement by phenoxides.
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| 22. | They also react with alkyl halides to form carbocations and.
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| 23. | Hydrogen iodide, like other hydrogen halides, is toxic.
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| 24. | Another route employs acyl halides instead of the carboxylic acid.
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| 25. | Some ytterbium halides are used as reagents in organic synthesis.
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| 26. | Unlike the halides, the alkoxides dissolve in nonpolar solvents.
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| 27. | The Appel reaction is also useful for preparing alkyl halides.
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| 28. | The halides, and the oxides and their derivatives are illustrative examples.
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| 29. | Lithium aluminium hydride also reduces alkyl halides to alkanes,.
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| 30. | Primary halides are the most reactive followed by secondary halides.
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