(9) 8. Show how you would accomplish the following multistep synthesis: Synthesize the insect repellent N,N-diethyl-n-toluamide...
The top half of the image depicts the reaction of the synthesis of N,N-diethyl-m-toluamide (DEET). The bottom half of the image attached shows the table of chemicals used in the reaction. How would I calculate the theoretical yield and furthermore, the percent yield? This experiment had a lot of chemicals used, and I don't know where to start. SOC (CH, CH2), NH -(CH₃ CH₂)₂NH₂ cr CN(CH₂ CH₂), - HD, -50, mame molecular formula Quantity density maar gwel thinyl chloride sou,...
Propose a stepwise mechanism for the synthesis of N,N-diethyl-m-toluamide (DEET). please show all steps! thanks (CH,CHy), WH -CH,CH) NHCr N(CH, CH,) SOCI -HCI CAM3 -5 CAM
Chem2020 Provide a multistep synthesis to accomplish the following transformations. Be sure to show all starting materials, reagents, reaction conditions, and products for each step. Each synthesis will be more than 1 step. +2 CO HO. OH c Chem2020 Provide a multistep synthesis to accomplish the following transformations. Be sure to show all starting materials, reagents, reaction conditions, and products for each step. Each synthesis will be more than 1 step. +2 CO HO. OH c
8. Devise a multistep synthesis for the following transformation. Show all intermediates and reagents. ??? Br Br (additional reagents must have no more than 2 carbons.)
6) Multistep synthesis from cyclohexane Using cyclohexane as your starting material, show how you would synthesize cach of the following compounds. Once you have shown how to synthesize a compound, you may use it as the starting material in any later parts of this problem.) a) bromocyclohexane (b) cyclohexene e) ethoxycyclohexane (d) 3-bromocyclohex-l-ene (e) cyclohexa-1,3-diene (1) cyclohexanol
① ( 38 Points) Synthesis for the cases below show how you would synthesize the desired product from the given starting material using any Reaction in Chapters 1-9, Use any recessary Reagents and any alcohol up to 6 carbons H-C=C-17 myh Acetylene Starting material heptanal starting maker
How would you synthesize each of the following from either ethyl acetoacetate or diethyl malonate? Show retrosynthesis and forward synthesis|. a) b)
8. Show how you would accomplish the following syntheses. You may use whatever additional reagents you need. The synthesis should not take more than three or four reactions. At least one of the reactions should come from the aldehydes and ketones chapter. (6 pts) a) CO2H b)
Show how you would accomplish each of the following multistep conversions. Include all reagents and condtitions and show all reaction products. 4. Al Use conditions to selectively make the Z-alkene
Show how you would synthesize the following a n d beginning with 1-butene, Bromma and any necessary additional reagents. More than one step is needed. Br Bromobenzene, 1-Butene < Show how you woull Synthesize 4.- Nonanone, begining with 1-Butanol and any other non-organic reagents. (1-Butanol is the only Organic compouno available). only organ n