16) Provide a synthesis for the following transformation. (8 points) O2N
5. (8 points) Devise a synthesis to the following target using both of the organic precursors from the chemical bank and any transformation we have learned in organic I and II. Target: Chemical Bank: CI он CI O O2N NO2
5. (8 points) Devise a synthesis to the following target using both of the organic precursors from the chemical bank and any transformation we have learned in organic I and II. Target: Chemical Bank: CI он CI O O2N NO2
Provide a synthesis for the following reaction
Provide a synthesis for the following transformation.
Synthesis. Provide a reasonable synthetic route for the following transformation: Provide the major product Please provide a mechanistic explanation for the following synthesis:
Provide multiple step synthesis scheme for the following
transformation.
Provide a synthesis for the following product
Provide reagents for the following transformation. If more than one step is required, number individual steps.
chemistry please help
16. (a) (6 points) Show how to accomplish the following synthesis. mia Eto OET ОН (b) (4 points) Propose an efficient synthesis for the following transformation. Br
Provide the reagents necessary for the following transformation. HINT: this is a multi-step synthesis. (10 pts) 9. ?? ?? ?? H2N
Use ANY needed reagents to effect the following transformation. Br ÇO2Et O2N starting material product
Provide a synthesis and mechanisms for the following transformation. Include all reagents and intermediate products. Please upload your answer as a PDF or Word document. H3CO
Synthesis please
Synthesis from benzene please.
NMe2 NH2 O2N CI ОН HO35 ZI