Starting with benzene and using any inorganic reagents, provide a stepwise synthesis of Benzylamine and the reaction conditions and give the major organic product for each step
Starting with benzene and using any inorganic reagents, provide a stepwise synthesis of Benzylamine and the...
u.Propose a synthesis of the following molecule from benzene and any organic or (" inorganic reagents necessary. In your synthesis, you can only separate isomers in the middle of the synthesis, the final step should give only the desired product. (Hint! Don't forget about carbocation rearrangements.)
1) Starting with methylcyclohexane and using any inorganc
reagents, peroxides or alkoxides provide a step-by-step synthesis
of a cyclohexanone (ketone) and carbone dioxide. Show the
reactants/conditions for each step and the major organic product
molecule for each step. Assume isomers can be separated (be regio-
and stereospecific)
2)
2. Fill in the major product/s or reagents wherever appropriate. Be regio- and stereo-specific. NBS, hy
Starting with nitrobenzene (PhNO2) and using any other inorganic reagents, synthesize phenol (PhOH). Show the conditions and major organic product for each step.
4. Synthesis. You may use benzene (that is the starting material for a), any organic reagents that contribute four or fewer carbon atoms to the final product, and any inorganic reagents OH OH HN NH
4. Synthesis. You may use benzene (that is the starting material for a), any organic reagents that contribute four or fewer carbon atoms to the final product, and any inorganic reagents OH OH HN NH
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic reagents, any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. (Bonus: make your cyclohex-2-enone using only the other reagents given) он
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic...
Provide a stepwise synthesis for the following reaction. you may
use the indicated starting materials as well as any organic or
inorganic reagents.
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic reagents any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. (Bonus: make your cyclohex-2-enone using only the other reagents given) other reagents glven) MS, Bones он
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons...
Please explain the mechanisms!
1. Propose a synthesis for each of the following problems starting with reagent shown and using any other organic or inorganic reagents allowed in each problem. Multiple steps are required. The number of steps you use does not matter. Reactions should give the desired product as a major product. For full credit show the product of each step (reaction). If you make use of organometallic reagents such as Grignard, Wittig, organolithium, organosodium, organocopper, etc. you must...
Name: 4. Starting with benzene and any inorganic or organic reagents, outline all steps in the synthesis of the following compounds. No mechanisms required but correct order is. (HINT: think clectrophilic aromatic substitution) (10 points): (A) (B)
Provide a synthetic route for the following compound from
benzene and any other necessary organic and inorganic reagents.
List the required reagents and conditions for each step and draw
the product for each step
14. Provide a synthetic route for the following compound from benzene and any other necessary organic and inorganic reagents. List the required reagents and conditions for each step and draw the product for each step. (4 pts) 0-V