ynthesis will take more than one step. For each reaction you use, show the reagents you would use and the product of that step. In each step, your desired product should be formed as the major product. Assume chiral products are formed as racemic mixtures. Your reactions should give the correct diastereomer. In addition to the provided starting material, you may use any other organic compound as well as any reagents we have discussed. Could someone please help me with this practice problem? Thank you
Propose a series of reactions that would convert the provided starting material into the given product. The synthesis will take more than one step. For each reaction you use, show the reagents you would use and the product of that step. In each step, your desired product should be formed as the major product. Assume chiral products are formed as racemic mixtures. Your reactions should give the correct diastereomer. In addition to the provided starting material, you may use any other organic compound as well as any reagents we have discussed.
Could someone please help me with this practice problem?
Thank you!
Terminal alkynes having hydrogen is attached to sp carbon is acidic in nature becuase in sp hybridization there are 50% s character. Hence, this carbon is more acidic as compared to sp2 and sp3 carbon.
The acidic hydrogen is abstracted and produces the carbanion.
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