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It is sometimes necessary to isomerize a cis
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- How could the following compund be prepared using an alkene as one of the starting materials? You can use the suitable reactives for this reaction while showing the reaction mechanism.arrow_forwardHow many alkene products, including E, Z isomers, might be obtained by dehydration of 3-methyl-3-hexanol with aqueous sulfric acid?arrow_forward6) 25pts. Draw the structure of the major alkene product (or products) formed by treatment of each of the following haloalkanes with sodium ethoxide in ethanol. Assume the mechanism is E2 elimination. t-BuO K t-BUOH Br CH3 Eto Na F ETOH CH2CH3 CI H- Eto Na -CH2CH3 ELOH H- ČH3 Br Eto Na ELOH CH3 CI, H Eto Na CH2CH3 H3C H D ELOHarrow_forward
- Which of the following reaction sequences would you use to convert 1- methylcyclohexene to the product 2 ? OH 2 O A) Oxymercuration-Demercuration O B) Hydroboration-Oxidation O C) Os04 / Pyridinc- NalHSO3 O D CH3CO3H- H30+arrow_forward6. Complete the following reduction reactions, Draw the structure of the product. Name tne reactant and product. a) Cty-CH-C=0 Ni + Hs It CH3 b) o-と-CH--cng Ni Ni c) CHy-CH-CHy + Hz CHz d) CH + Hz 7. Complete the following reactions for the formation of hemiacetals. Draw the structure of the product. Name the reactants. a) acid Cら-と-A + Ho-CHCH Sつっつ (。 + Ho-CH3 acid Ho-CH-CH, + C-CH-C-C-CH d CH3 c)arrow_forwardAnother important pattern in organic synthesis is the construction of C-C bonds. Us- ing your reaction roadmap as a guide, show how to convert propane into hex-1-en-4- yne. You must use propane as the source of all of the carbon atoms in the hex-1-en-4-yne product. Show all reagents needed and all molecules synthesized along the way. Propane Hex-1-en-4-ynearrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning