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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
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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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. mopeatane to athy alkene tat occus via a syn ion and drevs on occurs vi an anti addition d dras ia stte wote out two resctions on that Markov addition and notha tht kov parloway 5.) Devise a synthesis of CH3CH2CH2CHO from two-carbon starting materials. Draw both the retrosynthesis and the forward synthesis.
Transcribed Image Text: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. mopeatane to athy alkene tat occus via a syn ion and drevs on occurs vi an anti addition d dras ia stte wote out two resctions on that Markov addition and notha tht kov parloway 5.) Devise a synthesis of CH3CH2CH2CHO from two-carbon starting materials. Draw both the retrosynthesis and the forward synthesis.
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