:woled On each of the three resonance structure intermediates, for the Electrophilic Substitution Reaction v) shown below, first add the missing carbocation “ (+) “ charge and second show by drawing in the correct flow of electrons using arrows. 66 66 -E H. alod rwoda Н abogo Н H. vi) Reactions by E1/E2: Circle the two incorrect products and box the most stable alkene product in the reaction shown below. NaOH ETOH Br
:woled On each of the three resonance structure intermediates, for the Electrophilic Substitution Reaction v) shown below, first add the missing carbocation “ (+) “ charge and second show by drawing in the correct flow of electrons using arrows. 66 66 -E H. alod rwoda Н abogo Н H. vi) Reactions by E1/E2: Circle the two incorrect products and box the most stable alkene product in the reaction shown below. NaOH ETOH Br
Chemistry
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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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v and vi please

Transcribed Image Text::woled
On each of the three resonance structure intermediates, for the Electrophilic Substitution Reaction
v)
shown below, first add the missing carbocation “ (+) “ charge and second show by drawing in the
correct flow of electrons using arrows.
66
66
-E
H.
alod rwoda
Н
abogo
Н
H.
vi)
Reactions by E1/E2: Circle the two incorrect products and box the most stable alkene product in
the reaction shown below.
NaOH
ETOH
Br
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