n-propylbenzene can be synthesized in high yield by using indirect strategy. The detailed information is given below-
Design a synthesis of n-propylbenzene from benzene. Hint: A one-step synthesis using CH,CH CH Br and...
Starting from benzene and using any other necessary reagents of your choice, design a synthesis for each of the following compounds. Some problems have more than one plausible 1 answer (a) Cl. .NO2 (b) НAN. (c) H2N (d) (e) Br СООН СООН Br (g)* in this example, what can be done to minimise the amount of the meta/para isomes. NO2 (h) Br H2N Br Cl -NH2 Cl (k) Br
Starting from benzene and using any other necessary reagents of your choice, design a synthesis for each of the following compounds. Some problems have more than one plausible 1. answer (g)* in this example, what can be done to minimise the amount of the meta/para isomes. NO2 (h) रेर Br (i) Н-N. Br NH2 (k) Br "SoH
30 Design a synthesis of m-bromostyrene from benzene. points Br Part 1 out of 12 Choose the best option for the immediate precursor to the target molecule. Br points НО 23 Design a synthesis of p-t-butylacetophenone from benzene. points Choose the best option for the immediate precursor to the target molecule. Part 2 out of 6 Choose the best option for the precursor to t-butylbenzene. 2 points NH2 OH 23 points NH2 он
Please put all 6 steps. Design a synthesis of 2-bromo-1-chloro-4-nitrobenzene from benzene or any mono-substituted benzene. Cl Br benzene or any mono-substituted benzene NO2 Part 1 out of 6 Choose the best option for the immediate precursor to the target molecule. CI Br NO2
Starting with benzene and using any other neccessary reagents of your choice, design a synthesis for each of the following: OMe COOH Br Br NO NO (b) COOH NH Cl Cl NO2 COOH NO2 Cl NO Cl Br OEt NO2 Cl (h) C (g) NO2 Br O2N
using the reagents listed below, propose a synthesis of the target compound starting from benzene. Remaining Time 58 minutes, 36 send Question Completion Status Using the registed below, propone a thesis of the target compound starting from benzene. Enter your awwer as a lof letters corresponding to the selected register you wish to use them You may assume that all reactions appropriately worked up and that matures of construtorallomers can be separed. You may use a reagent more than one...
Starting from Benzene and using reagents that we have discussed in class, design a synthesis for the Target molecule (TM). TM SM
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
8. Design a synthesis of p-nitrotoluene, starting from benzene (3 pts). from to NO2 4 9. Are the following pairs identical, enantiomers, diastereomers, or constitutional isomers? (4 points) (a) Но, Contact and "CH2CH3 H3CH2C" (b) CH2OH CH2OH HO Н HO- -H and CI Н H CI CH3 CH3
20. Starting from benzene or anisole and any other reagent of your choice, design a synthesis for each of the following compounds. (18 pts) 21. Predict the products from the Birch reductions shown below. (3 pts) Na GLO Bonus: (6 pts) Provide a synthesis for the target molecule using benzene. COH COH TM