Organic chemistry: Overview of nucleophilic attacks on carboxylic acids and acid derivatives through the addition-elimination mechanism. How to make 1,3-dicarbonyls through the Claisen condensation; the Dieckmann condensation (intramolecular Claisen condensation). Reactions of 1,3-dicarbonyls—acetoacetic ester synthesis; malonic ester synthesis This is a recording of a tutoring session, posted with the students permission. These videos are offered on a "pay-what-you-like" basis. You can pay for the use of the videos at my website: http://www.freelance-teacher.com/videos.htm For a list of all the available video series, arranged in suggested viewing order, go to my website. For a playlist containing all the videos in this series, click here: http://www.youtube.com/watch?v=3N8rvTXfAnI&feature=PlayList&p=F860F2E81C2AE642&index=0&playnext=1 (1) Overview of nucleophilic attacks on carboxylic acids and acid derivatives through the addition-elimination mechanism (2) Continued. Claisen condensation (3) Continued (4) Continued (5) Continued (6) Continued. Dieckmann condensation (intramolecular Claisen condensation) (7) Continued. Claisen condensation with enolates formed from ketones (8) Synthesis with the Claisen condensation; retrosynthesis (9) Alkylation of 1,3-dicarbonyls. Decarboxylation (10) Continued (11) Continued. Acetoacetic ester synthesis (12) Continued (13) Malonic ester synthesis
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