Practice: Determine the product from the following Heck Reaction.
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Electron Configuration of Elements | 46 mins | 0 completed | Learn |
Coordination Complexes | 20 mins | 0 completed | Learn |
Ligands | 24 mins | 0 completed | Learn |
Electron Counting | 11 mins | 0 completed | Learn |
The 18 and 16 Electron Rule | 13 mins | 0 completed | Learn |
Cross-Coupling General Reactions | 40 mins | 0 completed | Learn |
Heck Reaction | 40 mins | 0 completed | Learn |
Stille Reaction | 14 mins | 0 completed | Learn |
Suzuki Reaction | 25 mins | 0 completed | Learn |
Sonogashira Coupling Reaction | 17 mins | 0 completed | Learn |
Fukuyama Coupling Reaction | 16 mins | 0 completed | Learn |
Kumada Coupling Reaction | 13 mins | 0 completed | Learn |
Negishi Coupling Reaction | 17 mins | 0 completed | Learn |
Buchwald-Hartwig Amination Reaction | 19 mins | 0 completed | Learn |
Eglinton Reaction | 18 mins | 0 completed | Learn |
Example #1: Determine the product from the following Heck Reaction.
Example #2: Rank the following alkenes in order of increasing reactivity towards the Heck Reaction.
Practice: Determine the product from the following Heck Reaction.
Practice: Predict the product formed from the following intramolecular Heck reaction.
Practice: Using ethyl-2-butenoate as your starting material, prepare the following compound by a Heck reaction.
Example #3: A Heck reaction between (Z)-3-hexene and bromoethene creates both (Z)-3-ethyl-1,3-hexadiene and (E)-3-ethyl-1,4-hexadiene. Illustrate how both products can be formed.
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