Show how to complete the following transformations. More than one step will be required.
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Show how to complete the following transformations. More than one step will be required. OH a...
2. Show how to complete the following transformations. More than one step will be required. OH -CO2CH2CH3 Na o H3C-CECH ОН. H3C-CECH H3C
3) Show how you would carry out the following transformations. More than one step is required. Use any organic or inorganic reagents that you need. Show all reagents and intermediate products. (24 pts) H2CH2C CH3 HEH HH OH + enantiomer | Ph = Ph- H + 4
complete the transformation and more than one step will be required. use any reagents and show all of them and intermediate structures 어 ОН Br don Br
Synthesis version: 7. Provide reagents for the following two transformations. If more than one step is required, number individual steps. Use your answers to 6a and 6b to help you with this! Br CH,CH3 + E H CIWC- H, OH HzC CH3 CEC CH,CHz . HC Br H C-CICH "CH + E HO CH2CH3
1) Show how you would make the following synthetic transformations. More than one step may be required. a) Benzene to 3,5-dibromo-1-ethylbenzene b) benzene to benzylamine (aminomethyl benzene, not aniline) c) benzene to benzonitrile d) methyl orange from sulfanilic acid
5. Provide the complete reaction conditions (reagents, solvents) required transformations. More than one step may be required for each reaction arrow, be numbered 1), 2) etc. (12 marks) ents, solvents) required to complete the following uired for each reaction arrow, in which case the steps must DO
Provide reagents for The following transformations. If more than one step is required, number individual steps.
2) Show how you would accomplish the following transformations. These are all essentially one step reactions (depending on how you count). OH Br OH OH OH он OH он 0 но
Please answer a-c 3. Show how you would carry out the following transformations. More than one step is required. Use any organic or inorganic reagents that you need. Show all reagents and intermediate products. Hint: Don't forget reactions you already learned from previous chapters. (16pt) sys
44. Propose efficient methods for accomplishing each of the following transformations. Most will require more than one step HO H Br meso-2R,35-isomer) H OH HO HO H (Racemate of 2R,3R and 2S,3S isomers) нон HO H но 44. Propose efficient methods for accomplishing each of the following transformations. Most will require more than one step HO H Br meso-2R,35-isomer) H OH HO HO H (Racemate of 2R,3R and 2S,3S isomers) нон HO H но