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Module 2 Alcohols, halogenoalkanes and analysis
Module 2 Alcohols, halogenoalkanes and analysis

... Figure 4 Oxidation reactions of three alcohols (labelled) by orange acidified potassium dichromate solution (H2SO4/ K2Cr2O7). The dichromate is reduced when it reacts, forming a green solution. Primary and secondary alcohols can be oxidised, forming carboxylic acids and ketones respectively. Tertiar ...
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Nucleophilic acyl substitution



Nucleophilic acyl substitution describe a class of substitution reactions involving nucleophiles and acyl compounds. In this type of reaction, a nucleophile – such as an alcohol, amine, or enolate – displaces the leaving group of an acyl derivative – such as an acid halide, anhydride, or ester. The resulting product is a carbonyl-containing compound in which the nucleophile has taken the place of the leaving group present in the original acyl derivative. Because acyl derivatives react with a wide variety of nucleophiles, and because the product can depend on the particular type of acyl derivative and nucleophile involved, nucleophilic acyl substitution reactions can be used to synthesize a variety of different products.
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