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