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Date: 27-9-2020
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Date: 1-8-2018
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Date: 24-9-2020
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Clemmensen Reduction
This alternative reduction involves heating a carbonyl compound with finely divided, amalgamated zinc. in a hydroxylic solvent (often an aqueous mixture) containing a mineral acid such as HCl. The mercury alloyed with the zinc does not participate in the reaction, it serves only to provide a clean active metal surface. The first example below shows a common application of this reduction, the conversion of a Friedel-Crafts acylation product to an alkyl side-chain. The second example illustrates the lability of functional substituents alpha to the carbonyl group. Substituents such as hydroxyl, alkoxyl & halogens are reduced first, the resulting unsubstituted aldehyde or ketone is then reduced to the parent hydrocarbon. A possible mechanism for the Clemmensen reduction will be displayed by clicking the "Show Mechanism" button.
Mechanisim
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تفوقت في الاختبار على الجميع.. فاكهة "خارقة" في عالم التغذية
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أمين عام أوبك: النفط الخام والغاز الطبيعي "هبة من الله"
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خدمات متعددة يقدمها قسم الشؤون الخدمية للزائرين
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