File:Benzaldehyde and diethyl malonate aldol addition.svg

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Español: La adición aldólica del malonato de dietilo 1 y el benzaldehído 2 conduce a un solo producto 3. El control se produce porque los átomos de hidrógeno α lábiles en 1 están doblemente activados por la presencia de dos grupos carbonilo adyacentes. El benzaldehído 2 carece de átomos de hidrógeno α lábiles. El enolato que se forma es del éster y se obtiene el producto de adición cruzada (el producto de autocondensación está inhibido estéricamente).
English: Diethyl malonate 1 and benzaldehyde 2 aldol addition, leading to a lone product 3. The chemical outcome is controlled because labile α-hydrogen atoms in 1 are highly activated because there are two adjacent carbonyl groups. Benzaldehyde 2 lacks labile α-hydrogen atoms. The enolate formed comes from the ester, so the crossed addition product is obtained (the self-addition product is sterically inhibited).
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Author Omegakent

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current21:22, 15 March 2010Thumbnail for version as of 21:22, 15 March 2010391 × 73 (16 KB)Omegakent (talk | contribs){{Information |Description={{es|1=La adición aldólica del malonato de dietilo '''1''' y el benzaldehído '''2''' conduce a un solo producto '''3'''. El control se produce porque los átomos de hidrógeno α lábiles en '''1''' están doblemente activado

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