8) Using benzene and any other reagents or catalysts, devise areaction to easily synthesize the following...
8) Using benzene and any other reagents or catalysts, devise grcaction to casily synthesize the following molecule: (20 pt.) CH3 -с-сн, CH3 9) Why have we discontinued use and/or made it illegal to use DDT and other halogenated pesticides in the United States? (10 pt.) 10) Predict the products for the following reactions: (20 pt.) a) (Spts.) FeBr3 - CH2- CH3 Br2 b) (5 pts.) ??? CH-C CH-CH HCI CH3 (5 pts.) ??? PEROXIDES - CHCH3 HCI CH3—С- CH3 (5...
E. Synthesis: 13 Points Synthesize the molecule below using any of the following reagents: benzene, bromobenzene, any alkenes, alcohols, or alkyl halides of three carbons or less, ethylene oxide; any inorganic reagents, oxidizing or reducing agents, and any peroxyacids. CH2CH3 CH2CH2N CH3 CH3 0%0% E. Synthesis: 13 Points Synthesize the molecule below using any of the following reagents: benzene, bromobenzene, any alkenes, alcohols, or alkyl halides of three carbons or less, ethylene oxide; any inorganic reagents, oxidizing or reducing agents,...
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic reagents any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. (Bonus: make your cyclohex-2-enone using only the other reagents given) other reagents glven) MS, Bones он Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons...
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic reagents, any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. (Bonus: make your cyclohex-2-enone using only the other reagents given) он Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic...
show how to synthesize this molecule using benzene, 1-bromocyclopenta-1,4-diene and any other reagents containing less than two carbons. steriochmistry does matter this is for organic chemistry 2 so the synthesis should involve reactions covered in that class such as a diels-alder reaction or using a organolithium reagent о: т
. Starting with acetylene, any halide ($4C), and any other reagents required, synthesize the target molecule. (8 pts) TM Starting with acetylene, any halide (S4C), and any other reagents required, synthesize the target molecule. (7 pts) 2. OH TM
E Synthesis: (17 Points) Noting stereochemistry, synthesize the molecule below using any of the following reagents: alkanes, alkenes, or alkynes having no more than two carbon atoms, any inorganic reagents, any oxidizing or reducing agents, any peroxyacids, benzene, and phenol. (깨
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformation in good yield. Use the given compounds as the only organic source of carbon atoms. You may use any common organic solvents as well as any needed inorganic reagents (14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI....
Synthesis 18.63) Synthesize each compound from benzene and any other organic or inorganic reagents. Br- CICINO, OYNH2 COOH O2N. -C NH2 НО ОН SO3H HOOC (PABA) sunscreen component
6. Starting with benzene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there may be more than one plausible answer 7. Starting with benzene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there may be more than one plausible answer 8. Starting with benene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there...