Design a synthesis of the following target molecule from cyclohexane. Make sure it is at least 4 steps long.
Design a synthesis of the following target molecule from cyclohexane. Make sure it is at least...
Design a 4 step synthesis of the following target
molecule form cyclohexane. Name all the organic products for each
step.
Br
Design a 4 step synthesis of the following target
molecule from any alkene. Name all the organic products in each
step.
— О
3. Design a synthesis of the following molecule starting from
benzene and molecules of two or less carbon atoms. You are not
limited in your choice of reagents or number of steps.
ΝΟ2 ΝΗ2 12 Br 10 Cl CO2H он CI
ΝΟ2 ΝΗ2 12 Br 10 Cl CO2H он CI
Provide multistep synthesis for the following target molecule from
the indicated starting materials
NH2 from 0 from NO2 Br
(B) () Devise a synthesis of the following "target molecule" from the given starting material.(i) Also, expláin why you would make this "target molecule" this way rather than a one-step synthesis of monoalkylating ammonia (NH3). from: NH2 HN I TARGET MOLECULE Hydro lysis
Design a synthesis of the target from the starting material and
any other reactants and reagents.
4) Br
Propose a synthesis using the target molecule with
retrosynthetic analysis.
Provide complete reagents for each step of your proposed
synthesis.
from Target molecule
from Target molecule
4. Design a synthesis for the following molecule. You may only use carbon containing reagents if they are in the list on the right. You may use any other non-carbon containing reagents that you would like. Target molecule: Carbon containing molecules that you may use (you don't have to use all of them): -Br Out NaCN Br CO2
Concept- Design a synthesis of 4-Cyanocyclohexene Design a synthesis of 4-cyanocyclohexene from 2-bromopropanenitrile and any other compounds using a Diels-Alder cycloaddition reaction. CN Br CN and any other compounds Part 1 out of 7 Choose the best option for the diene precursor to the target molecule CN diene dienophile CN CN
Design an efficient synthesis for the following target molecule, using any hydrocarbons with three or less carbon atoms as starting materials to build the target molecule; also using any solvents or reagents that do not contribute carbon atoms to the final structure. SHOW YOUR ANSWER AS A STEPWISE REACTION SCHEME SHOWING THE REAGENT REQUIRED AND PRODUCT OF EACH STEP DO NOT SHOW MECHANISMS (i.e. curly arrows are NOT required) Any solvents or reagents that do not contribute carbon atoms to...