Please draw the appropriate reagent(s) required to accomplish for each of the indicated transformations. You can assume that more than one step would be necessary to accomplish the synthesis. H₂N CH3 OH
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- Draw the structures of all possible products formed from the following reaction. Specifiy the type of substitution or elimination pathway. Demonstate the stereochemical outcomes of the reaction by drawing your products in wedge dash form when necessary.How would you convert cyclohexanone to each of the following compounds?If the following sesquiterpene is synthesized in a medium containing acetate with a 14C-labeled carbonyl carbon, which carbons will be labeled?
- 1) Please draw the mechanism for the following transformation. он NABH4 ELOHdraw a correct mechanism to react with 2-methylocta-4,6-dien-1-amine with the given reagent. Again, disregard any parts of the molecule represented by R-groups and focus on the given portion of the molecule. Be sure the correct mechanism arrives at the correct product of the reaction. The incorrect mechanism may or may not have the correct productProvide a synthesis for the following transformation OH
- Match each reagent to the product that it forms. Multiple reagents may form the same product. нох Reagent Reagents SOCI2, pyridine: C CISO2CH3, pyridine: E HCI: A PCI 3: A A) B) "It "ft "bl H₂O D) E) F) پہلے علی علیہThe following molecule undergoes an intramolecular reaction in the presence of pyrrolidinium acetate, the protonated form of pyrrolidine. Draw the product of this reaction, assuming that a dehydration reaction takes place.Identify the lettered compounds in each reaction sequence.Draw the product formed when phenylacetonitrile (C6H5CH2CN) istreated with below reagent. H2O, −OH