Mechanism of alkaline hydrolysis of bromoethane
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in the alkaline hydrolysis of esters and amides the hydroxide ion nucleopjile attacks the carbonyl carbon in a nucleophilic acyl substitution reaction . this mechanism is supported by isotopes labeling experiments .
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in the alkaline hydrolysis of esters and amides the hydroxide ion nucleopjile attacks the carbonyl carbon in a nucleophilic acyl substitution reaction . this mechanism is supported by isotopes labeling experiments .
I hope this answer helps u
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Explanation:
Alkaline hydrolysis, in organic chemistry, usually refers to types of nucleophilic ... absent from the sodium propionate product and is found exclusively in the ethanol formed .
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