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Question Description: Although there are two different bromine leaving groups in the cyclohexane derivative shown below, only one of them can be eliminated in this reaction. 2 Br Br NaOEt 2 3 6 4 5 EtOH 1144: Instructions: Investigate the reaction shown above and to clearly explain why the product provided for you forms exclusively by completing the following items: a Indicate what type of reaction is shown above. Briefly discuss the stereoelectronic/sigma-bond alignments required for this reaction to take place. Draw both chair conformations for the starting cyclohexane derivative and circle the one that is most relevant for undergoing the reaction indicated. Specifically, how does this chair Conformation satisfy the stereoelectronic/sigma-bond requirements indicated in item 2? C) Draw a complete arrow-pushing mechanism to illustrate the electron flow in the reaction.
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EtoA By EtoH By tr1 NooH u

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