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Chemistry
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ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Transcribed Image Text:6. Suggest a synthesis for the following product starting with benzene. You may use any other organics or inorganics.
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Br
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- Draw balanced chemical equations for the Birch reduction of the following benzene derivatives. Please explain steps 1a)Anisole 1b) Aniline 1c) Phenol 1d) Toluenearrow_forwardPropose a multi-step synthetic route to form the polycyclic molecule on the right hand side using the following reagents on the left hand side of the arrows: i) cyclic ketone; ii) a,ẞ-unsaturated ketone; iii) either the organocuprate OR the organolithium reagent listed; and ii) any other reagents or solvents of your choosing The depicted reagents represent all necessary building blocks that are directly incorporated into the molecule on the right, however you should use additional reagents to help facilitate its construction based on Chem 110 content from Chapters 21 and 23. This is a multi-step synthesis and not all reagents will be used at the same time. When describing your solution, show the stable intermediates along your proposed synthetic route and number the individual synthetic steps. You do not have to worry about stereochemistry in this particular question. For two (2) of your proposed steps, show individual mechanistic arrows that show the flow of electrons during that…arrow_forwardDevise concise syntheses for the following transformations. Clearly show the reagent and product foreach step.arrow_forward
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