Скачать или смотреть Making Triptycene with the Weird Molecule Benzyne

Benzyne is one of the most reactive and unstable organic intermediates, but today, we’re harnessing its power to synthesize Triptycene, a fascinating molecular structure that resembles a paddlewheel. This experiment dives into the chemistry behind benzyne generation, the Diels–Alder reaction, and the step-by-step process of making triptycene in the lab.

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References and uses:
Adams, R., Johnson, J. R., & Wilcox, C. F. (1979). Laboratory experiments in Organic Chemistry. Macmillan.
Noyes, W. A. (n.d.). n-BUTYL NITRITE. Organic Syntheses. http://www.orgsyn.org/Content/pdfs/pr...
PhET Simulation: Ideal Gas Law. (PhET, Boulder). Retrieved March 5, 2023, from https://phet.colorado.edu/en/simulati....
Jmol: an open-source Java viewer for chemical structures in 3D. http://www.jmol.org/

Chapters:
00:00 Introduction
00:38 n‑butyl nitrite synthesis
06:47 Solvent Problem
09:14 Triptycene Synthesis
09:30 Reaction Rate
11:10 Triptycene Synthesis Cont.
15:05 Analysis

Thanks for watching!