Question
Write chemical reactions for the following:
(i) Kolbe Schmidt reaction
(ii) Strecker synthesis
(iii) Dieckmann cobndensation
(iv) Knoevenagel reaction
(v) Perkin condensation
Answer :
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The Kolbe–Schmitt reaction proceeds via the nucleophile addition of a phenoxide, classically sodium phenoxide (NaOC6H5), to carbon dioxide to give the salicylate. The final step is reaction of the salicylate with acid to form the desired salicylic
The Strecker synthesis is a two-stage procedure used to synthesize alpha amino acids from aldehydes.
Deprotonation of an ester at the α-position generates an enolate ion which then undergoes a 5-exo-trig nucleophilic attack to give a cyclic enol. Protonation with a Brønsted-Lowry acid (H3O+ for example) re-forms the β-keto ester.
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