1) The compound below is (1S,2R)-1-bromo-1,2-diphenylpropane. H. Br NOTE: For i) and i) below, be sure to include curved arrows, lone pairs, formal charges. Please abbreviate the phenyl ring substituents in your answers as 'Ph'. i) Using perspective diagrams, draw the product(s) of, and show a curved arrow mechanism for, the elimination reaction which would take place between (1S,2R)-1-bromo-1,2-diphenylpropane and NaOH (i.e. hydroxide ion, HO). Name the product(s). Is the process stereoselective or stereospecific? If stereoselective, indicate the major product. ii) Using perspective diagrams, draw the product(s) of, and show a curved arrow mechanism for, the elimination reaction which would take place between (1S,2R)-1-bromo-1,2-diphenylpropane and methanol, CH3OH. Name the product(s). Is the process stereoselective or stereospecific? If stereoselective, indicate the major product.

1) The compound below is (1S,2R)-1-bromo-1,2-diphenylpropane. H. Br NOTE: For i) and i) below, be sure to include curved arrows, lone pairs, formal charges. Please abbreviate the phenyl ring substituents in your answers as 'Ph'. i) Using perspective diagrams, draw the product(s) of, and show a curved arrow mechanism for, the elimination reaction which would take place between (1S,2R)-1-bromo-1,2-diphenylpropane and NaOH (i.e. hydroxide ion, HO). Name the product(s). Is the process stereoselective or stereospecific? If stereoselective, indicate the major product. ii) Using perspective diagrams, draw the product(s) of, and show a curved arrow mechanism for, the elimination reaction which would take place between (1S,2R)-1-bromo-1,2-diphenylpropane and methanol, CH3OH. Name the product(s). Is the process stereoselective or stereospecific? If stereoselective, indicate the major product.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterL4: Proton (1h) Nmr Spectroscopy

Section: Chapter Questions

Problem 18CTQ

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