As learned in the synthesis of 1-bromo-3-chloro-5-iodobenzene, electron donating groups enhance the reactivity of benzene tawards electrophiles and electron withdrawing groups decrease the reactivity of benzene towards electrophiles. Based on this, which of the following benzene derivatives is the MOST REACTIVE towards electrophiles? NO2 NH: HN O A. 3 O B. 4 OC.1 O D. 2

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Chapter1: Chemical Foundations
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QUESTION 15
As learned in the synthesis of 1-bromo-3-chloro-5-iodobenzene, electron donating groups enhance the reactivity of benzene tawards electrophiles,
and electron withdrawing groups decrease the reactivity of benzene towards electrophiles. Based on this, which of the following benzene
derivatives is the MOST REACTIVE towards electrophiles?
NH,
NO,
NH2
O A. 3
O B. 4
O C.1
O D. 2
QUESTION 16
Select the most acidic proton
the molecule shown below.
Click Save and Submit to save and submit. Click Save All Answers to save all answers.
nere to search
N
PrSc
*-
F11,
F12
F10
F7
Esc
F3
F4
&
@
%23
.7
8
9.
3
4.
T
U
KL
G H
S
LK
B NM
C V
Transcribed Image Text:QUESTION 15 As learned in the synthesis of 1-bromo-3-chloro-5-iodobenzene, electron donating groups enhance the reactivity of benzene tawards electrophiles, and electron withdrawing groups decrease the reactivity of benzene towards electrophiles. Based on this, which of the following benzene derivatives is the MOST REACTIVE towards electrophiles? NH, NO, NH2 O A. 3 O B. 4 O C.1 O D. 2 QUESTION 16 Select the most acidic proton the molecule shown below. Click Save and Submit to save and submit. Click Save All Answers to save all answers. nere to search N PrSc *- F11, F12 F10 F7 Esc F3 F4 & @ %23 .7 8 9. 3 4. T U KL G H S LK B NM C V
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