Design a synthesis of 4,4-dimethyl-2-cyclohexenone from any acyclic compounds.
Design a synthesis of 4,4-dimethyl-2-cyclohexenone from any acyclic compounds.
Design a synthesis of 2-cyclohexenone from 2-methylcyclopentanone. &-& Part 1 out of 10 Choose the best option for the precursor to the target molecule. الله
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
condensed structure fir 4,4-dimethyl-2-hexanol
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
4. Design a synthesis to make the following compounds -och- from T H and A and any other reagents jom from He
Synthesis Experiment #2: Design syntheses to produce the following compounds starting with ethylene and any methyl halide. Note that once a compound has been synthesized in one process it can be used in a different process if you reference where it was first made.
Devise a synthesis of (Z)-4,4-dimethyl-2-pentene using one of the starting materials and any of the reagents below using the fewest steps possible. If you need fewer than the 3 steps allowed, enter "none" for reagents in the remaining unused steps. Starting materials HCBCH HC=C–CH, HC=C=CH-CH, HC=C=CH-CH-CH-CH, остаток сн. HC=C–C–CH, Η. сн. HC=C–C–CH, CH, . Reagents a NaNH, NHI) diodoethane g 1-bromo-3-methylbutane į Hy / Lindlar catalyst b NaOH ІН,0 e 1-bromopropane ht-butyl bromide k H, NH (1) c iodomethane f...
Design an effective synthesis for each of the following amino acids starting from the compounds shown on the left. You may also use any monofunctional organic compound containing four or less carbon atoms, and any inorganic reagents in your syntheses.
20. Starting from benzene or anisole and any other reagent of your choice, design a synthesis for each of the following compounds. (18 pts) OCH
Give the products (if any) expected from the treatment of each of the following compounds with ozone followed by dimethyl sulfide.A. 3-methyl-2-pentane _______ + (CH3)2SOB. _______ + (CH3)2SO