1. indicate the reagents, in the correct order, needed to
perform the transformations shown below. More than one step will be
needed.
2. explain why only one product is made and not the other.
Include use of the mechanism and appropriate drawings.
3. clearly explain why the alkyl bromide below produces mostly
substitution product under one set of conditions, but yeilds almost
exclusivly elimination products with a slight change in
conditions.
Show transcribed image text 5.(4 pts ca) Indicate the reagents, in the correct order, needed to perform the transformations shown below. More than one step will be needed DM50 But I RCE RECOH. Y MSO CH, Oct> OCH 6.(6 pts)Explain why only one is and not the other use of the product made . Include mechanism and appropriate drawings. Ph CH H Br NaOCH Ph Ph Ph PT CH CHOH HCHg Ph Product not produced S7rcadou The Porbitals of Phoe-s much formation of a double bond which will cause overlap and Oh thcarbons . eng 7(6pts)Clearly explain why the alkyl bromide below produces mostly substitution product under one set of conditions, but yields almost exclusively elimination products with a slight change in conditions Ethanol X — LCD A AM 3; NOEt 99 Ethanol In the substitution reacHon the ethanol acts as a strong nucleophie, which favors substitut on because Chronoſ wi U also fore onitoon. In the elimination reaction the N-OE+ wi | as a weak base ushnick will accopt the 4¢ grader Omnia.
5.(4 pts ca) Indicate the reagents, in the correct order, needed to perform the transformations shown below. More than one step will be needed DM50 But I RCE RECOH. Y MSO CH, Oct> OCH 6.(6 pts)Explain why only one is and not the other use of the product made . Include mechanism and appropriate drawings. Ph CH H Br NaOCH Ph Ph Ph PT CH CHOH HCHg Ph Product not produced S7rcadou The Porbitals of Phoe-s much formation of a double bond which will cause overlap and Oh thcarbons . eng 7(6pts)Clearly explain why the alkyl bromide below produces mostly substitution product under one set of conditions, but yields almost exclusively elimination products with a slight change in conditions Ethanol X — LCD A AM 3; NOEt 99 Ethanol In the substitution reacHon the ethanol acts as a strong nucleophie, which favors substitut on because Chronoſ wi U also fore onitoon. In the elimination reaction the N-OE+ wi | as a weak base ushnick will accopt the 4¢ grader Omnia.
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