Design a synthesis of ethyl N-(ethylimino)propanoate from ethyl formate, ethyl acetate, and ethyl propanoate. and CH3CH2...
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 p-t-butylacetophenone from benzene and choose the best option for the immediate precursor to the target molecule. Design a synthesis ofp-t-butylacetophenone from benzene. Part 1 out of 6 Choose the best option for the immediate precursor to the target molecule. OH
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 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
30 Design a synthesis of m-bromostyrene from benzene. points Br Part 1 out of 12 Choose the best option for the immediate precursor to the target molecule. Br points НО 23 Design a synthesis of p-t-butylacetophenone from benzene. points Choose the best option for the immediate precursor to the target molecule. Part 2 out of 6 Choose the best option for the precursor to t-butylbenzene. 2 points NH2 OH 23 points NH2 он
Please design a synthesis for trans-2-methycyclopentanol into 8 parts. Design a synthesis of trans-2-methylcyclopentanol from methylenecyclopentane. CH3 ??! Part 1 out of 8 Choose the best option for the immediate precursor to the target molecule. CH3 ?? A CH3 CH3 CH2 ?? CH3
Help Save & Exits Amines Part 2 out of 11 Choose the best option for the nucleophile precursor to the target molecule. US CHCH2 nucleophile OCH CH3 OCH2CH3 A CH3CH2 B (CH,CH), C (CH,CH, NH но осн,Сн,он 6 CH,CHẠNH, < Prev 16 of 44 ! Next > MacBook Air
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 N,N-diethyl-1-methyl-1-phenyl-1-propen-1-amine from benzaldehyde and any compound containing three carbons or fewer. V // and any compounds containing three carbons or fewer Part 1 out of 13 Choose the best option for the nucleophile precursor to the target molecule. nucleophile electrophile 7 Z // HH B H2N
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