4) Design a synthesis for the following molecule from any 3 carbon haloalkane
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
Design a 4 step synthesis of the following target molecule from any alkene. Name all the organic products in each step. — О
4. Design a synthesis for the following molecule. You may be use carbon containing reagens they are in the list on the right. You may use any other non-carbon containing reagents staining recents that you would like. Target molecule: Carbon containing molecules that you may use you don't have to use all of them): NaCN CO2 5. Predict the products of the following reaction and draw a detailed step wise mechanism H20 H30+
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...
3) Propose a synthesis scheme for the following molecule from benzene using any reaction conditions. 4) Propose a synthesis scheme for the following molecule from benzene using any reaction conditions. NH2
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
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
Design a synthesis of the following target molecule from cyclohexane. Make sure it is at least 4 steps long. muli Br
Starting with a 4-carbon alcohol, a 4-carbon diol, and ethanol, design a synthesis for 3-ethyl-2-heptanone. (please show mechanism)
3. Design a synthesis of the molecule at right from an organometallic reagent and: он a) a ketone b) a different ketone c) an ester