3. Propose a synthesis for the following? Remember it's more than 1 step [6]
Propose a synthesis for the following conversion. It will take more than one step. Show the product of each reaction you propose to use. [6 points] CN
Propose a synthesis for the following transformation. More than one step is required. NO2 НО,
8 This synthesis requires more than 1 step-propose a route giving all reagents (include solvents) required and drawing the structure of all stable, neutral intermediate compounds. [6 pts 9. Nether of the reactions drawn below will give the product shown. Draw the product that will form instead giving a mechanism as an explanation. [10 pts) HBr ether Br 11. Are these statements True or False? (2 pts each = 4 pts] a) Fluoride ion is a more reactive nucleophile in...
22 Name: ID: A 4. Propose a synthetic route which includes more than one step to carry out the following transformation (6 pts) vi ?vi S. Briefly explain why the following reaction would be unsuccessful. (6 pts) 6. Fill in the missing reagents and intermediates to complete the synthesis below. (8 pts) 1. NO 1. NaOH
1) Propose a synthesis of the following 2) Propose a synthesis. HOL 3) Propose a synthesis. 4) Provide the structure of the polyamide formed in this reaction. H2O) Polyamide Heat 5) Propose a synthesis. 2 / OH
Propose methods for each of the following syntheses. More than one step is necessary in each synthesis. Show the complete mechanism using curved arrow formalism for each step. (a) cyanocyclohexane from cyclohexanol (b) (S)-2-cyanobutane from (S)-2-chlorobutane (c) cyclohexyl methyl ether from any alcohol and any haloalkane (d) 1,1-dichloro-2,2,3,3-tetramethylcyclopropane from 2-bromo-2,3dimethylbutane
Show a good laboratory synthesis of the following compounds. If more than one step is required, provide each step in the synthesis, reagents required for the step, and write the structures of the products of each step.
4. 1) LIAIH 2) H20 5. Propose an efficient synthesis for one of the following transformations. Please circle the synthesis you are completing. More than one step will be required; be sure to number each step. It will be significantly easier to award partial credit if you show the intermediate product after each step. CN Br ОН OR OH + enantiomer
4. Propose a synthetic pathway for the following reaction (there may be more than one correct way), then show the mechanism for each step (Hint: To save time make sure your synthesis pathway is absolutely coret before you work on mechanism) но Br
3. Propose a plausible synthesis for each of the following transformations: 3. Propose a plausible synthesis for each of the following transformations: 2x - 2 x 2x 0-5 •♡-