Q5(a). Condensation of diethyl succinate
Diethyl succinate is treated with NaOEt/EtOH to give A, followed by aqueous NaOH and heating to give B. Identify A and B and explain step 1.
Answer in brief
A is diethyl 2,5-dioxocyclohexane-1,4-dicarboxylate (diethyl succinylsuccinate); hydrolysis, acidification and decarboxylation give cyclohexane-1,4-dione B.
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CoversClaisen condensationdiethyl succinylsuccinatecyclohexane-1,4-dionedecarboxylationDieckmann condensation
All parts of Question 5
- 5(a) Condensation of diethyl succinate5 marks
- 5(b) DNA bases and pairing5 marks
- 5(c) Vinylcyclopropane rearrangement5 marks
- 5(d) Oxidation of 2-acetylpyridine5 marks
- 5(e) Azobenzene and hydrazobenzene5 marks
- 5(f) Nitration of indole5 marks
- 5(g) Acidity of cyclopentadiene derivatives5 marks
- 5(h) Photoproducts of ketone excitation5 marks