7. Please design a synthesis of the following compound using 2 equivalents of but-1-ene as your starting materials and source of carbon and any inorganic reagents you wish. Goal Pfar 29NAM
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- 5. Synthesize the following compounds by using cyclohexanone and propene as your only sources of carbon. Any other needed reagents are available.4) Provide a synthesis of the following compounds using the given starting material and any other reagents. starting material final product CI starting material final product OH OH OH starting material final product 5) Provide an arrow-pushing mechanism for the following reaction to get to the product shown. HON OH H₂O*, H₂O НО ملهProvide a synthetic route for the following transformation: Please provide steps and type of reactions as well as using commercially available reagents, with an explanation of steps. OH N. H
- Devise a synthesis of (E)-tetradec-11-enal, a sex pheromone of the spruce budworm, a pest that destroys r and spruce forests, from acetylene, Br(CH2)10OH, and any needed organic compounds or inorganic reagents.H₂C CH3 Show how the compound can be synthesized from benzene and alkyl chlorides.1. Propose reasonable syntheses for each of the following compounds from given starting materials. You may use any organic or inorganic reagent ( НО OH OH НО OH ОН Хон
- Fill in the missing reagents a-e in the following scheme:Using your reaction roadmap as a guide, show how to convert cyclohexane into hexanedial. Show all reagents and all molecules synthesized along the way.Devise a synthesis of (E)-tetradec-11-enal, a sex pheromone of the spruce budworm, a pest that destroys fir and spruce forests, from acetylene, Br(CH2)10OH, and any needed organic compounds or inorganic reagents.
- Devise a synthesis of CH3CH2C≡CCH2CH2CH3using CH3CH2CH=CH2as the starting material. You may use any other organic compounds or inorganic reagents.Alkyl diazonium salts are unstable even at low temperature. They decompose to form carbocations, which go on to form products of substitution, elimination, and (sometimes) rearrangement. Keeping this in mind, draw a stepwise mechanism that forms all of the following products. NANO2 он + HCI, H2O NH2 онDraw the major organic product of the following reactions. Include all arrows and steps BV NA OCH3 CH3OH 1. LDA 2.