| | LECTURE 5 |
 | | The cannizaro reaction is very slow and as such an advantage is taken of the time lag to synthesis polyhydroxy compounds using such aldehydes in cross-aldol condensation as carbanion acceptors. |
 | | A controlled reaction of Aldol formation followed by elimination of water is called the Claisen-Schmidt condensation of aromatic aldehydes with aliphatic aldehydes or ketones in the presence of 10% mineral alkali. |
 | | In aldol condensation, nucleophilic attack leads to addition, which is a typical reaction of aldehydes and ketones, whereas in claisen condensation, the nucleophilic attack leads to substitution, which is also the typical reaction of acyl compounds. |
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