Design a synthesis of N,N-diethyl-1-methyl-1-phenyl-1-propen-1-amine from benzaldehyde and any compound containing...
Design a synthesis of 2-ethyl-N,N-dimethyl-5-hexen-1-amine from any cyclic secondary amine containing only C, H, and N. CH₃ any cyclic secondary amine containing only C, H, and N CH3 1 1 Part 1 out of 6 Choose the best option for the immediate precursor to the target molecule. CHE N CH3 A H C CH3 N CH3 CH3 C HCTCH, © Br. CH3
Design a synthesis of ethyl 2-ethyl-3-oxohexanoate from alcohols containing 4 carbons or fewer. points COET alcohols containing 4 carbons or fewer Part 1 out of 9 Choose the best option for the precursor to the target molecule. Part 2 out of 9 19 Choose the best option for the carboxylic acid precursor to the intermediate ethyl butanoate. points TOET OET carboxylic acid alcohol oị © © carboxylic acid alcohol points ОН он о носH,CH, но Design a synthesis of ethyl...
Design a synthesis of ethyl N-(ethylimino)propanoate from ethyl formate, ethyl acetate, and ethyl propanoate. and CH3CH2 OCH2CH3 OCH2CH3 OCH CH3 OCH CH3 Part 1 out of 11 Choose the best option for the immediate electrophile precursor to the target molecule. CH3CH2 nucleophile OCH2CH3 electrophile А) C3 CH3CH2 A CH3CH2 OH OCH2CH3 CH3CH20 OCH2CH3 D CH3CH2 CH3CH2
Part 9 out of 11 6 Choose the most appropriate reagent(s) for the conversion of 1-butanol to butanal. PCC CH2Cl2 points COH Cl2 FeCl3 OH reagent(s) Trayers) points A NaOH,H,O, heat B PCC, CH.CH C 1.0 ) LAIH, diethyl ether 2. S(CH) e Na Cr»0», H,804, H,0 13 Design a synthesis of 2-cyclohexenone from 2-methylcyclopentanone. points Part 1: Choose the best option for the precursor to the target molecule. i i Part 2 out of 10 Choose the best option...
Concept- Design a synthesis of 4-Cyanocyclohexene Design a synthesis of 4-cyanocyclohexene from 2-bromopropanenitrile and any other compounds using a Diels-Alder cycloaddition reaction. CN Br CN and any other compounds Part 1 out of 7 Choose the best option for the diene precursor to the target molecule CN diene dienophile CN CN
Design a synthesis of ethyl 3-10-2,4-diphenylbutancate from alcohols possessing eight carbons or fewer.Choose the best option for the immediate precursor to the target molecule.
Design a synthesis of ethyl 3-oxo-2,4-diphenylbutanoate from alcohols possessing eight carbons or fewer. Ph OEt - alcohols possessing eight carbons or fewer Part 1 out of 9 Choose the best option for the immediate precursor to the target molecule. ther OEt Ph
Design a synthesis of 1-chloro-2-propanol from 1-propanol.Choose the best option for the immediate precursor to the target molecule.An alkene can be used to introduce both an alcohol and a halide functional group to each of the carbons of the double bond in a controlled and predictable manner in one step. Choose the best option for the precursor needed to make the alkene.
Design a synthesis of (Z) 5-methyl-2-hexene from propyne and 2-methyl-1-propanol. H -CH3 and OH Part 1 Choose the best option for the immediate precursor to (Z) 5-methyl-2-hexene. CH Br Br This alkyne can be converted to (z 5-methyl-2-hexene in one step. Part 2 out of 9 Choose the best option for the nucleophile precursor to 5-methyl-2-hexyne. CH3
Amine Synthesis I Prepare the following compounds from any simple alcohol containing four carbons or less, benzene, toluene, and/or cyclohexane. Be sure to show all steps, reagents used, etc. 2. NH2 NH2 3. 6. 5. NH2 NH2 NHCH2CH3 7. 10. NHCH CH3 9. Amine Synthesis I Prepare the following compounds from any simple alcohol containing four carbons or less, benzene, toluene, and/or cyclohexane. Be sure to show all steps, reagents used, etc. 2. NH2 NH2 3. 6. 5. NH2 NH2...