Indicate the preferred product of the following reaction, as learned in the synthesis of 1-bromo-3-chloro-5-lodobenzene. NO2 SnHCI NaOH NH, NH2 NO: NO. 3 O A. 1 O B. 2 OC.4 O D.3

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QUESTION 14
Indicate the preferred product of the following reaction, as learned in the synthesis of 1-bromo-3-chloro-5-iodobenzene.
NO2
SnHCI
NaOH
NH,
NH2
NO,
1
3
O A. 1
O B. 2
O C. 4
O D.3
QUESTION 15
As learned in the synthesis of 1-bromo-3-chloro-5-iodobenzene, electron donating groups enhance the reactivity of benzene towards electrophile
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?
NH2
NO:
NH:
Click Save and Submit to save and submit. Click Save All Answers to save all ansuers.
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Transcribed Image Text:Question Completion Status: QUESTION 14 Indicate the preferred product of the following reaction, as learned in the synthesis of 1-bromo-3-chloro-5-iodobenzene. NO2 SnHCI NaOH NH, NH2 NO, 1 3 O A. 1 O B. 2 O C. 4 O D.3 QUESTION 15 As learned in the synthesis of 1-bromo-3-chloro-5-iodobenzene, electron donating groups enhance the reactivity of benzene towards electrophile 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? NH2 NO: NH: Click Save and Submit to save and submit. Click Save All Answers to save all ansuers. N here to search F10 F11 F12 F7 F8 Esc F4 F5 F1 F2 F3 ! %23 $4 % & .7 8. 9. 1 4. T Y U Q W G H J KL LL
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