alkyl halide การใช้

• In a related reaction, alkyl halides undergo nucleophilic displacement by phenoxides.
• They also react with alkyl halides to form carbocations and.
• The Appel reaction is also useful for preparing alkyl halides.
• Lithium aluminium hydride also reduces alkyl halides to alkanes,.
• Heating alkyl halides with sodium hydroxide or water gives alcohols.
• The Wurtz reaction reductively couples two alkyl halides to couple with sodium.
• Metal acetylides can be coupled with primary alkyl halides.
• Vinyl, aryl and tertiary alkyl halides are unreactive.
• Secondary alkyl halides are coupled with aryl silanes with good yields using this reaction.
• Deprotonation with lithium diisopropylamide and addition of an alkyl halide affords the alkylated product.
• Alkyl halides differ greatly in the ease with which they undergo the Finkelstein reaction.
• The latter reaction is also significant for involving a traditionally inaccessible alkyl halide coupling.
• This transformation include alkylations with other classes of activated alkyl halides of synthetic interest.
• However, phenols can be used to replace the alcohol, while maintaining the alkyl halide.
• Chemically, halothane is an alkyl halide ( not an ether like many other anesthetics ).
• As mentioned above, the Wittig reagent itself is usually derived from a primary alkyl halide.
• Additionally, the presence of ?-hydrogens makes alkyl halides susceptible to competitive elimination processes.
• The compound is used as a reagent for the preparation of primary amines from alkyl halides.
• The coupling of alkyl halides with organo-halo-silanes as alternative organosilanes has also been performed.
• Silanes can also incorporate the same functional groups as alkanes, e . g . alkyl halide ).