Devise a synthesis for the following compounds from benzene, any alcohol with four or fewer carbos, and any other required reagent NH 0 .N. CN
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- Devise a synthesis of each compound from cyclopentanone, benzene, and organic alcohols having ≤ 3 C's. You may also use any required organic or inorganic reagentsDevise a synthesis of each compound from CH3CH2CH2CO2Et, benzene, andalcohols having ≤ 2 C's. You may also use any required organic or inorganic reagents.Devise a synthesis of each compound from cyclohexene as the starting material. More than one step is needed.
- Capsaicin, the spicy component of hot peppers, can be prepared from amine X and acid chloride Y. Devise a synthesis of Y from (E)-6-methylhept-4-en-1-ol [(CH3)2CHCH=CH(CH2)3OH], CH2(CO2Et)2, and any required inorganic reagents.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.Devise a synthesis of the ketone hexan-3-one, CH3CH2COCH2CH2CH3, from CH3CH2Br as the only organic starting material; that is, all the carbon atoms in hexan-3-one must come from CH3CH2Br. You may use any other neededreagents.
- Devise a synthesis of each compound from benzene. You may also useany organic compounds having four or fewer carbons and any requiredinorganic reagents.The key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold Helminthosporium sativum, involves the following base treatment of a keto tosylate. What kind of reaction is occurring? How would you complete the synthesis?Draw the structure of Kodel, a polyester prepared by heating dimethyl 1, 4-benzenedicarboxylate with 1, 4-bis(hydroxymethyl)cyclohexane.
- A key step in the synthesis of the antidepressant paroxetine (trade name Paxil) involves a Williamson ether synthesis of the acyclic ether in X. Draw two different routes to this ether and state which is preferred.Devise a synthesis of each compound from cyclohexene as the startingmaterial. More than one step is needed.Devise a synthesis of the following compound from styrene. You may use any inorganic or organic reagents. More than one step is required. C6H5CH(OH)CH2C≡CH