1) PCC is the first reagent we
are using for the selective oxidation of OH group.
2) then use any chlorinating agent like PCl5 which will remove one hydrohen.
3) allow the chlorinated product to react with anilinium ion which remove HCl to get the product.
in the image after the last (final arrow) the answer is the product of the reaction mentioned in question.
e an efficient multi-step synthesis for the following molecule starting from the compourd shown on the...
9. P ropose a multi-step synthesis to accomplish the overall transformation shown below (make the molecule on the right starting with the molecule on the left). Show all necessary reagents and products for each forward step. [It is not necessary to show any mechanisms.] OH 10. Propose a multi-step synthesis to accomplish the overall transformation shown below (make the molecule on the right starting with the molecule on the left). Show all necessary reagents and products for each forward step....
Justify answers.
Propose a multi-step synthesis to accomplish the overall transformation shown below (make the molecule on the right starting with the molecule on the left). Show all necessary reagents and products for each forward step. OH
3. Devise a multi-step synthesis of the target molecule from the given starting material. Show all necessary reagents and conditions for each step and the product of each step. (7) OH
3. Devise a multi-step synthesis of the target molecule from the given starting material. Show all necessary reagents and conditions for each step and the product of each step. (7) OH BONUS: Please provide the arrow pushing mechanism of this reaction. Be sure to show a charges and stereochemistry where needed. To receive full credit, what is the name of this reaction? (4) NaOE HOE Br
Devise a multi-step synthesis
of the target molecule from the given starting material. Show all
necessary reagents and conditions for each step and the product of
each step.
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Provide a multi-step synthesis for the following target molecule from the indicated starting material. T- from OH and он
1. Starting with benzene and any necessary reagents, design an efficient synthesis of the following compound: 1. Provide a detailed curved-arrow mechanism to account for the transformation below and explain why the only products formed at high and low temperatures are the ones shown. (Show all resonance contributors for all intermediates): HCl, Clos Cocha осн
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 all
8. Provide an efficient multi-step synthesis of 2 starting with 1. In your forward synthesis, indicate the reagents used for each step by writing them over the arrow leading to cach of the specified products. At some point in your synthesis you must utilize the chemical(s) specified over the arrows. opo maeneo l 5. Draw the major product for each of the following reactions or reaction sequences. Show stereochemistry where appropriate. Assume aqueous workup. 1) Fe, HCI...
5. Provide a synthesis for each molecule shown below starting from the indicated compound. In addition to the starting material, you may use any necessary reagents. OH a. Eto Et