E2 elimination , epoxidation followed by acid in the presence of ethanol gives the final product.
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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
From the table of reagents shown below, show how you synthesize the product from the given reactant. Reagents available (Enter the letter(s) of the reagent(s) needed in the box, in the order that they must be used. No more than two steps are required to perform the synthesis. Note that a retrosynthetic arrow is used, and therefore the reactant is shown on the right.) Answer:
Show how you can synthesize the compound from a benzene Show how you can synthesize the compound from benerene COOH - Br NH2
1)How would you synthesize the following product from the assigned reactants? a. You have to show the shortest and most effective reaction schemes using the ONLY given compounds as carbon sources to make the product. You can use proper reagent(s) for each step. b. Only two reactants allowed to build the carbon backbone are shown below. c. Explain how you would confirm each step using 1H-NMR, 13C-NMR, IR, and UV-Vis spectroscopie. (no spectrums needed) o - and to make Use
Show how you would synthesize the following compounds from 1-methylene cyclopentane Q3. (i) Show how you would synthesize the following compounds from (Note; More than one step may be required) (8) - CH2 a). - NAPH NHPh
sbow how you woukd synthesize each of the following compounds from benzene (a) Show how you would synthesize each of the following compounds from benzene. Br (b) (c) (d) NHA Br. Br. (e) HN NH2
show the steps required to synthesize the product from the given starting material 6ts n Show the steps required to synthesize the product from the given starting material. (6pts) Question 11 6 pts OH Upload Choose a File
Show how you would synthesize 4-bromo-2-nitrotoluene from benzene.
Show how to synthesize the target molecule from the given material as the only source of carbon. Show the reagents needed for each step and the product of each step.
What is the major product from a reaction of nitrobenzene with Fe/HCL? How would you synthesize 3-chlorobenzoic acid, starting with benzene?