Consider the molecule 3-hexyne, shown helow tf vou partially hydrogenated the molecule (1.e. generated nnalkene, rather than an alkane) and then treated the tina alken clemental bromine, illustrate the resultsif you hydrogenated over the Lindlar catalyst compared to hydrogenation via lithium or sodium in ammonia.CHgCH2C=CCH2CH3Alkynes can be directly reacted with elemental bromine as well. Assuming that you could control this process tolimit it to a single addition (i.e. generate an alkene), what would happen if you reacted first with bromine andthen hydrogenated the result? Explain in the context of your answer above.

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alkene, rather than an alkane) and then treated the resulting alkene with elemental bromine, illustrate the results Consider the molecule 3-hexyne, shown below. If vou natially hydrognated the molecule (ie. generaa a if you hydrogenated over the Lindlar catalyst compared te hydroeenation via lithium or sodium in ammonia CH3CH2C=CCH2CHS

alkene, rather than an alkane) and then treated the resulting alkene with elemental bromine, illustrate the results Consider the molecule 3-hexyne, shown below. If vou natially hydrognated the molecule (ie. generaa a if you hydrogenated over the Lindlar catalyst compared te hydroeenation via lithium or sodium in ammonia CH3CH2C=CCH2CHS

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter8: Haloalkanes, Halogenation, And Radical Reactions

Section8.6: Allylic Halogenation

Problem 8.5P: Given the solution to Example 8.5, predict the structure of the product(s) formed when 3-hexene is...

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Given the solution to Example 8.5, predict the structure of the product(s) formed when 3-hexene is treated with NBS.
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