4.) Use retrosynthetic analysis to show how hex-3-yne can be prepared from acetylene and anyother organic and inorganic compounds. Then draw the synthesis in the synthetic direction,showing all needed reagents.mopeatane to athyalkene tat occus via a synion and drevsonoccurs vi an anti addition d dras iasttewote out two resctions on thatMarkovaddition and notha thtkov parloway5.) Devise a synthesis of CH3CH2CH2CHO from two-carbon starting materials. Draw boththe retrosynthesis and the forward synthesis.

In presence of BH3 , H2O2/OH- , alkyne group converts into aldehyde or keto group. This is…

4.) Use retrosynthetic analysis to show how hex-3-yne can be prepared from acetylene and any other organic and inorganic compounds. Then draw the synthesis in the synthetic direction, showing all needed reagents. opentane to ahyl occus vin a syn fon and draws on oocurs via an an additiond dra stte FDefine Mar addition and another th nd wote oul woresclions that urkovnikov patloway 5.) Devise a synthesis of CH3CH2CH2CHO from two-carbon starting materials. Draw both the retrosynthesis and the forward synthesis.

4.) Use retrosynthetic analysis to show how hex-3-yne can be prepared from acetylene and any other organic and inorganic compounds. Then draw the synthesis in the synthetic direction, showing all needed reagents. opentane to ahyl occus vin a syn fon and draws on oocurs via an an additiond dra stte FDefine Mar addition and another th nd wote oul woresclions that urkovnikov patloway 5.) Devise a synthesis of CH3CH2CH2CHO from two-carbon starting materials. Draw both the retrosynthesis and the forward synthesis.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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