Chemistry
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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please just fill out reaction coordinate diagram
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?
expand button
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.
expand button
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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