Lecture 32 - Stereotopicity and Baeyer Strain Theory, Organic Chemistry
Rating
0 Visits
0 Ratings
Duration:
N/A
Source:
ACADEMIC EARTH
Found: Nov 3, 2009
Why ethane has a rotational barrier is still debatable. Analyzing conformational and configurational stereotopicity relationships among constitutionally equivalent groups reveals a subtle discrimination in enzyme reactions. When Baeyer suggested strain-induced reactivity due to distorting bond angles away from those in an ideal tetrahedron, he assumed that the cyclohexane ring is flat. He was soon corrected by clever Sachse, but Sachse’s weakness in rhetoric led to a quarter-century of confusion.
Please note that Find Internet TV does not host any videos or allow users to upload videos. The video is provided and hosted from a third party server. The source is noted to the right of the video and depending on the source, the author and copyright may be listed as well. The information provided here is aggregated from the source and provided by video search engines. Find Internet TV does not host and is not responsible for the content.