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Question 5 (27 pts.) Synthesize the target) molecules on the right from the starting molecules the...
Question 5 (27 pts.) Synthesize the target) molecules on the right from the starting molecules the...
Question 5 (27 pts.) Synthesize the target) molecules on the right from the starting molecules the left, this can not be done in one reaction. Give reagents and conditions and the intermediate molecules at each step. Do not show any mechanisms or transient intermediates. If other isomers are formed at any step then you need to indicate this but you do not need to draw their structures. NOZ CO2H SOH
22. Show how you would make the target compounds on the right form the starting compounds on the left. Show reagent...
22. Show how you would make the target compounds on the right form the starting compounds on the left. Show reagents and conditions where appropriate, and the structures of important intermediate compounds. Do not show any (arrow pushing) mechanisms!!!! (8 points) NH2 3-Steps NH2 17. Show the products and give reaction mechanisms for the following, using curved arrows to indicate the flow of electrons between intermediates.
please help asap Question 3 (36 pts.) For each of the following reactions: a) Provide the...
please help asap
Question 3 (36 pts.) For each of the following reactions: a) Provide the missing major organic product. Pay attention to stereochemistry unless directed otherwise and identify any racemic mixtures using the (1) symbol. c) Assign each reaction as OXIDATION or REDUCTION as appropriate NaBH, ETOH 1. Excess LIAIH 2. H2O nyomas La Na, Cr20;/H,SO/H, Excess PCC/CH_C12 OH Question 4 (22 pts.). Synthesize the target) molecule on the right from the starting molecule the left Give reagents and...
Design a multi-step synthesis for each of the following target molecules from the indicated starting material....
Design a multi-step synthesis for each of the following target molecules from the indicated starting material. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Draw the structures of the diene and the dienophile that reacted to form the Diels-Alder product shown. Provide the missing reagents in this multistep synthesis.
please solve thank you now how you would make the target compounds on the right form...
please solve
thank you
now how you would make the target compounds on the right form the starting npounds on the left. Show reagents and conditions where appropriate, and the structures of important intermediate compounds. Do not show any (arrow pushing) mechanisms!!!! A (6 pts) 2 Steps CH3 27 B (6 pts) 2 Steps Et B (7 pts) NH2 Et 2 Steps
5. Show how to synthesize the following molecules using the given starting material. Show all the...
5. Show how to synthesize the following molecules using the given starting material. Show all the intermediate products for multiple steps. You can use any other reagents or starting materials necessary D amer --
For 1 - 3, design reasonable syntheses of each of the target molecules using the provided...
For 1 - 3, design reasonable syntheses of each of the target molecules using the provided starting material and organic and inorganic reagents of your choice. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Please put all your answers on this sheet. Write your answers like this (actual number of starting steps may vary)material reagent(s) reagent(s) ABCD target Two equally reasonable routes are possible Can you find them both? (For...
Starting with benzene and any reagents you need, synthesize compound shown. More than one step is...
Starting with benzene and any reagents you need, synthesize compound shown. More than one step is required. Assume you can separate ortho and para-isomers. (12 pts) _CHâ‚‚
2. Devise a multistep synthesis of the target molecule from the starting material shown. Show the...
2. Devise a multistep synthesis of the target molecule from the starting material shown. Show the reagents needed for each step and the product of each step. Do not show any mechanisms.
4. In each reaction show how you would synthesize the product from the reactant. Show the...
4. In each reaction show how you would synthesize the product
from the reactant. Show the reagents, conditions, and the
structures of any important intermediates along the way. Any
organic reagent may be used, and more than one step may be used as
well. Include mechanism
(+-) H Br
Question 5 (27 pts.) Synthesize the target) molecules on the right from the starting molecules the left, this can not be done in one reaction. Give reagents and conditions and the intermediate molecules at each step. Do not show any mechanisms or transient intermediates. If other isomers are formed at any step then you need to indicate this but you do not need to draw their structures. NOZ CO2H SOH
22. Show how you would make the target compounds on the right form the starting compounds on the left. Show reagents and conditions where appropriate, and the structures of important intermediate compounds. Do not show any (arrow pushing) mechanisms!!!! (8 points) NH2 3-Steps NH2 17. Show the products and give reaction mechanisms for the following, using curved arrows to indicate the flow of electrons between intermediates.
please help asap
Question 3 (36 pts.) For each of the following reactions: a) Provide the missing major organic product. Pay attention to stereochemistry unless directed otherwise and identify any racemic mixtures using the (1) symbol. c) Assign each reaction as OXIDATION or REDUCTION as appropriate NaBH, ETOH 1. Excess LIAIH 2. H2O nyomas La Na, Cr20;/H,SO/H, Excess PCC/CH_C12 OH Question 4 (22 pts.). Synthesize the target) molecule on the right from the starting molecule the left Give reagents and...
Design a multi-step synthesis for each of the following target molecules from the indicated starting material. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Draw the structures of the diene and the dienophile that reacted to form the Diels-Alder product shown. Provide the missing reagents in this multistep synthesis.
please solve
thank you
now how you would make the target compounds on the right form the starting npounds on the left. Show reagents and conditions where appropriate, and the structures of important intermediate compounds. Do not show any (arrow pushing) mechanisms!!!! A (6 pts) 2 Steps CH3 27 B (6 pts) 2 Steps Et B (7 pts) NH2 Et 2 Steps
5. Show how to synthesize the following molecules using the given starting material. Show all the intermediate products for multiple steps. You can use any other reagents or starting materials necessary D amer --
For 1 - 3, design reasonable syntheses of each of the target molecules using the provided starting material and organic and inorganic reagents of your choice. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Please put all your answers on this sheet. Write your answers like this (actual number of starting steps may vary)material reagent(s) reagent(s) ABCD target Two equally reasonable routes are possible Can you find them both? (For...
Starting with benzene and any reagents you need, synthesize compound shown. More than one step is required. Assume you can separate ortho and para-isomers. (12 pts) _CHâ‚‚
2. Devise a multistep synthesis of the target molecule from the starting material shown. Show the reagents needed for each step and the product of each step. Do not show any mechanisms.
4. In each reaction show how you would synthesize the product
from the reactant. Show the reagents, conditions, and the
structures of any important intermediates along the way. Any
organic reagent may be used, and more than one step may be used as
well. Include mechanism
(+-) H Br
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