Reduction of nitro group to amine with iron and acetic acid
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Reduces aldehydes and ketones to corresponding alcohols. Sodium borohydride is not reactive to esters, epoxides, lactones, carboxylic acids, nitro compounds and nitriles, but reduces acyl chlorides. In combination with CeCl3 allows for selective reductions of α,β-unsaturated carbonyls without reacting with С=С-bonds.
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it is the reduction of nitro group admin with iron and acetic acid
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