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Claisen condensation. 1,3-dicarbonyls (11)

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. [8:00] 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. [3:00] Acetoacetic ester synthesis (12) Continued (13) Malonic ester synthesis
Length: 11:00

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