6. Devise a synthesis of molecule 1 using compound only sources of carbons. You can use any appropriate orga ecule...
6. Devise a synthesis of molecule 1 using compounds A, B, C, and D, compounds A, B and C are your only sources of carbons. You can use any appropriate organometallic and inorganic reagents as long as they are relevant to your synthesis. Show all your steps clearly, Recall: Aldehydes are typically more reactive that ketones. CH3CH2! OHC Php CHME
2) Devise a synthesis of the following compound using only ethanol. You may also use any needed Inorganic or organic reagents but all of the carbons in the target molecule must come from ethanol. Hint: this synthesis will require you to use a Claisen reaction
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...
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 synthesis of the following compound using the given compounds (you may use each one more than once if needed). You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials.
need help with this one 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
3) Devise a synthesis of the following compound using the given compounds (you may use each one more than once if needed). You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials. Hint: this synthesis will require you to use ozonolysis and a reaction that starts with the letter DI
9. Devise a synthesis of the following compound using the given lactone. You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials.
9. Devise a synthesis of the following compound using the given lactone. You may also use any needed inorganic or organic reagents but all of the carbons in the target molecule must come from the given starting materials.
Using any of the reagents drawn below as the only sources of the carbons in your target molecule, propose a multistep synthesis for the molecule drawn in the box below. Show all reagents and intermediate products that are formed in each step of the way. (8 pts) Reagents - Only Source of Carbons corocco tante como Target Molecule Using any of the reagents drawn below as the only sources of the carbons in your target molecule, propose a multistep synthesis...