Which, reagent combination will achieve this transformation? CN Ho но- A) 1) HBr 2) NaCN 3) H20 B) 1) NaCN 2) H2SO4 C) 1) MСРВА 2) NaCN 3) H20 D) None of the above O A O B O C O D
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- Which will complete the following reactions? Choices: A. HBr / ether B. PBr3 / ether C. SOCl2 / pyridine D. Br2 / NBS E. Chlorocyclopentane F. Cyclopentanol G. IodobenzeneProvide the reagents necessary to affect each transformationPlease give IUPAC names and R/S and E/Z designations for each molecule.
- First calculate r value of each then draw all possible structural and stereochemical isomers. Include enols and enamines and any e and z isomers. -C3H4O -C3H6O -C4H8O -C4H9Nhi! i need answers on letters d to f. The instructions says give the IUPAC name of each compound. Thank u!Hi! Could someone help me find the correct IUPAC names for these compounds and their stereochemistry? I’ve done everything else but these two are tripping me up for some reason. Thanks!!!
- Could you help explain each product?Heating an alcohol in the presence of sulfuric or phosphoric acid will cause a dehydration to occur: the removal of the elements of water from a molecule, forming an alkene. The reaction usually follows an E1 mechanism. The SN1 pathway is suppressed, both by heating the reaction mixture (more energy promotes the elimination pathway) and by using a strong acid whose conjugate base is a poor nucleophile. Draw curved arrow(s) to show how the alcohol reacts with phosphoric acid.please help with this question. thank you. identify the starting material to make each acetal.