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- Why does the final product has the opposite configuration compared to the reactant? Shouldn’t it form OMs first, then OMs gets substituted by Cl- via Sn2 (the 1st inversion of configuration) then the Cl- gets substituted by OCH3- (the 2nd inversion of configuration? To my understanding 2 inversions = same configurationProduct the product from the reaction. Then provide an electron push mechanism for the reaction. Solve it asapWhat is the main product of the following reaction? Please show all the steps of the mechanism
- Which statement best describes the stereochemistry of the product?For 10.29, the trans product (major product) and the cis product (third product) are displayed as possible E2 products. However, for 10.30, only the trans product (major product) is shown. How come the cis product is not needed?Please give full reaction in ha Identify the product of this reaction
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