Elimination of hydrogen bromide to form alkenes [E1 and E2].
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Conversion of an alcohol to a halogenoalkane. Elimination of water from an alcohol to give an alkene [acid catalysed, E1 and E2]. Nucleophilic addition of hydrogen cyanide to form a hydroxy-nitrile.
The iodination of ketones e. Hydrolysis of acid chlorides with water to give a carboxylic acid.
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Esterification of acid chlorides with alcohols to give an ester. Amide formation from reaction of acid chlorides with ammonia or primary amines. Nitration to give nitro-aromatics like nitrobenzene. Chlorination to chloro-aromatics like chlorobenzene. Please wait while we load your content Something went wrong. Try again? Cited by.
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Back to tab navigation Download options Please wait Article type: Review Article. DOI: Download Citation: Org. Hypervalent iodine reactions utilized in carbon—carbon bond formations I. Hyatt, L. Dave, N. David, K. Kaur, M. Medard and C.
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Mowdawalla, Org. Search articles by author I. Dempsey Hyatt. Loma Dave. Navindra David. Kirandeep Kaur. Marly Medard. View WJEC revision.
View Eduqas revision. Summary Alkyl halides are organic compounds containing carbon — halogen bond. The polarizability of carbon — halogen bond greatly influences the chemical reactivity of alkyl halides. Alkyl halides undergo nucleophilic substitution reaction.
Substitution reaction can follow SN1 or SN2 mechanisms. Both mechanisms follow different conditions and offer different products. Alkyl halides also form important Grignard Summary Chloroalkanes are organic compounds containing carbon and chlorine atoms. These organic compounds pose serious threat to our lovely planet. They are responsible for ozone depletion. The chemical reaction for ozone depletion is catalyzed by UV radiations.
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Comprehensive efforts are in place now to combat emission of these chloroalkanes Montreal protocol has been a great