(a)
Interpretation: The Wittig reagent and carbonyl compound that are needed to prepare the given
Concept introduction: One should follow the two steps retrosynthesis to find out the starting materials that are needed to prepare the given alkene. The first step is cleaving of
(b)
Interpretation: The Wittig reagent and carbonyl compound that are needed to prepare the given alkene are to be predicted, and the preferred route is to be identified, if any.
Concept introduction: One should follow the two steps retrosynthesis to find out the starting materials that are needed to prepare the given alkene. The first step is cleaving of
(c)
Interpretation: The Wittig reagent and carbonyl compound that are needed to prepare the given alkene are to be predicted, and the preferred route is to be identified, if any.
Concept introduction: One should follow the two steps retrosynthesis to find out the starting materials that are needed to prepare the given alkene. The first step is cleaving of
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ORGANIC CHEMISTRY BOOK& SG/SM
- Draw the organic products formed when each alkyne is treated with two equivalents of HBr.arrow_forwardDraw the structure of a dihalide that could be used to prepare each alkyne. There may be more than one possible dihalide.arrow_forwardWhat product is formed when each alkene is treated with HCl?arrow_forward
- Draw the products formed when each alkyne is treated with O3 followed by H2O.arrow_forwardWhat Wittig reagent and carbonyl compound are needed to prepare each alkene? When two routes are possible, indicate which route, if any, is preferred.arrow_forwardDraw the products formed when each alkene is treated with Grubbs catalyst.arrow_forward
- Using ethynylcyclohexane as a starting material and any other needed reagents, how can the following compounds be synthesized?arrow_forwardWhat alkyne yields each ketone as the only product both with acid-catalyzed hydration and after hydroboration–oxidation?arrow_forwardWhat is the major monobromination product formed by heating each alkane with Br2?arrow_forward
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