Show by means of retrosynthesis, synthetic schemes and EXPLANATORY NOTES, how would you carry out the following synthesis shown below. You are allowed to use any other reagents and starting materials you choose as long as the chosen substance(s) is/are used properly. Remember the principles of selectivity and control, and note any regiochemical or stereochemical problems that may possibly arise. Provide BRIEF NOTES and COMMENTS for EACH of the steps made, indicating any special reaction conditions, catalysts and solvents normally associated with the transformations that you propose. Reaction mechanisms are not required, however, remember the notes aforementioned. Please comment on what is happening at each step of the retrosynthesis.
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Show by means of retrosynthesis, synthetic schemes and EXPLANATORY NOTES, how would you carry out the following synthesi...
show how to carry out the following synthetic transformations using any compounds with one or two carbon atoms, any necessary solvents, and any Inorganic reagents. Clearly indicate reaction conditions. More than one synthetic step will be required (work backwards!) 1-Bromopentane- 2-Chloropenia H-C=C-H H₃C Br H-C=C-H - Br CH3 CHO H-C=c-H HO HIC TOH meso H-C=C-H c=CH₂ H3C CH(CH2).CHCI - CH(CH2),CHCHCI Наснас н H3CH2CCECH 4 CH₂CH₃ H3CH2CCECCH2CH3 Br Br CH,CH,CHCHCH.CH meso trans Ph trans OH show in most stable chair conformation)...
? How would you carry out the following conversion? Show only the reagents needed for each step and the structure of any intermediate formed with appropriate stereochemistry if necessary. More than one step may be necessary. No need to provide mechanisms but make sure you clearly indicate all reagents and intermediates. etb eo h flowing cosvesian? [10 marks] OH HO HO