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ih vghene In icho (OM bela bru Ol b) Using the axes below, draw a complete reaction coordinate diagram for the formation of both products from D-Br addition to 1,3 butadiene. Be sure to show the structures of the starting materials, intermediates and respective products on the diagram. c) Finally, on the diagram, clearly indicate which pathway would be favored at low temperature and which pathway would be favored at high temperature. laldho E arfa0ste worla anollbse piwollof er vo aloubong 1o alnse reaction progress

ih vghene In icho (OM bela bru Ol b) Using the axes below, draw a complete reaction coordinate diagram for the formation of both products from D-Br addition to 1,3 butadiene. Be sure to show the structures of the starting materials, intermediates and respective products on the diagram. c) Finally, on the diagram, clearly indicate which pathway would be favored at low temperature and which pathway would be favored at high temperature. laldho E arfa0ste worla anollbse piwollof er vo aloubong 1o alnse reaction progress

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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vOTene Inee alsdicho alk LOM bala br OMOH copria b) Using the axes below, draw a complete reaction coordinate diagram for the formation of asrig-niwode ol aho both products from D-Br addition to 1,3 butadiene. Be sure to show the structures of the starting materials, intermediates and respective products on the diagram. c) Finally, on the diagram, clearly indicate which pathway would be favored at low temperature and which pathway would be favored at high temperature. lition E paerlaoeste worla.anoloss piwollot erl ol alaubong 1o alns reaction progress What are wou the following 3. In an allylic bromination (i.e. with NBS), why is it essential to keep the concentration of molecular bromine relatively low?
Transcribed Image Text:vOTene Inee alsdicho alk LOM bala br OMOH copria b) Using the axes below, draw a complete reaction coordinate diagram for the formation of asrig-niwode ol aho both products from D-Br addition to 1,3 butadiene. Be sure to show the structures of the starting materials, intermediates and respective products on the diagram. c) Finally, on the diagram, clearly indicate which pathway would be favored at low temperature and which pathway would be favored at high temperature. lition E paerlaoeste worla.anoloss piwollot erl ol alaubong 1o alns reaction progress What are wou the following 3. In an allylic bromination (i.e. with NBS), why is it essential to keep the concentration of molecular bromine relatively low?
2. Consider the reaction below. Provide the two possible products that result from the addition of DBr to 1,3-butadiene. H-Br DBr Br 1 equivalent BY a) Next, show a curved arrow mechanism that accounts for both products. + BY - Br resonance J + Br > N Br 3.
Transcribed Image Text:2. Consider the reaction below. Provide the two possible products that result from the addition of DBr to 1,3-butadiene. H-Br DBr Br 1 equivalent BY a) Next, show a curved arrow mechanism that accounts for both products. + BY - Br resonance J + Br > N Br 3.
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