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1R,2S-dibromocyclododecane from acetylene and anything with 10 carbons or less. To do this problem, you must realize that a 12-membered ring unlike cyclohexene can be Z or E. Think of cyclohexene which only exists as the "Z" form and what product it forms with Br2 or maybe better, 2-butene which has two possible diastereomers and which diastereomer would form 2R,3S-dibromobutane.

1R,2S-dibromocyclododecane from acetylene and anything with 10 carbons or less. To do this problem, you must realize that a 12-membered ring unlike cyclohexene can be Z or E. Think of cyclohexene which only exists as the "Z" form and what product it forms with Br2 or maybe better, 2-butene which has two possible diastereomers and which diastereomer would form 2R,3S-dibromobutane.

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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Supply synthetic routes to the following molecules using the indicated starting materials

To synthesize 1R,2S-dibromocyclododecane from acetylene and any compound comprising 10 or fewer carbons, one must understand that a 12-membered ring, unlike cyclohexene, has the potential to exist in a Z or E configuration. Consider cyclohexene, which is restricted to the “Z” form. When reacted with Br₂, determine the outcome, or alternatively, examine 2-butene which presents two possible diastereomers. Identify which diastereomer leads to the formation of 2R,3S-dibromobutane.
Transcribed Image Text:To synthesize 1R,2S-dibromocyclododecane from acetylene and any compound comprising 10 or fewer carbons, one must understand that a 12-membered ring, unlike cyclohexene, has the potential to exist in a Z or E configuration. Consider cyclohexene, which is restricted to the “Z” form. When reacted with Br₂, determine the outcome, or alternatively, examine 2-butene which presents two possible diastereomers. Identify which diastereomer leads to the formation of 2R,3S-dibromobutane.
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