Pls help ASAP Using the reagents below, list in order (by letter, no period) those necessary to transform benzene into p-chlorobenzenesulfonic acid.You may assume any undesired regioisomers can be separated.Note: Not all spaces provided may be needed. Type "na" in any space where you have no reagent.A.H₂, PdB.H2, Pd/CaSO4, quinoline M. SOCI₂2C. H₂, Ni₂B(P-2)N. Br2, FeBr 3D. Zn(Hg), HCI, refluxO. Cl2, hvE. i.O3, H₂O ii. Zn, H₂OP. Cl2, FeCl3F. MMPP, CH3CH₂OHQ. H₂OG. i. BH3; ii. H₂O2, NaOHR. CH3CH₂CH₂CI, AICI 3H.KOC(CH3)3, HOC(CH3)3S. (CH3)3CCI, AICI3PapaL.HCI, peroxide ■niKalincI. HNO3, H₂SO4J. SO3, H₂SO41K. HCI, CH3CH₂OCH₂CH3 V.Step #1T. CH3 CH₂CH₂-C2016-1U. CH₂ CH₂NStep #2CICICI, AICI 3, AICI 3, AICI 3ΝΑStep #3ΝΑStep #4

Chlorination:-Benzene can react with Cl2, FeCl3 and forms chlorobenzene as a product.This is…

Using the reagents below, list in order (by letter, no period) those necessary to transform benzene into p-chlorobenzenesulfonic acid. You may assume any undesired regioisomers can be separated. Note: Not all spaces provided may be needed. Type "na" in any space where you have no reagent. A.H₂, Pd B.H₂, Pd/CaSO4, quinoline M. SOCI₂ C. H₂, Ni₂B(P-2) N. Br2, FeBr 3 D. Zn(Hg), HCl, reflux O. Cl₂, hv E. i.O3, H₂O ii. Zn, H₂O P. Cl2, FeCl3 F. MMPP, CH3CH₂OH Q. H₂O G. i. BH3; ii. H₂O2, NaOH R. CH3CH₂CH₂CI, AICI 3 H.KOC(CH3)3, HOC(CH3)3 S. (CH3)3CCI, AICI 3 L. HCI, peroxide

Using the reagents below, list in order (by letter, no period) those necessary to transform benzene into p-chlorobenzenesulfonic acid. You may assume any undesired regioisomers can be separated. Note: Not all spaces provided may be needed. Type "na" in any space where you have no reagent. A.H₂, Pd B.H₂, Pd/CaSO4, quinoline M. SOCI₂ C. H₂, Ni₂B(P-2) N. Br2, FeBr 3 D. Zn(Hg), HCl, reflux O. Cl₂, hv E. i.O3, H₂O ii. Zn, H₂O P. Cl2, FeCl3 F. MMPP, CH3CH₂OH Q. H₂O G. i. BH3; ii. H₂O2, NaOH R. CH3CH₂CH₂CI, AICI 3 H.KOC(CH3)3, HOC(CH3)3 S. (CH3)3CCI, AICI 3 L. HCI, peroxide

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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Question

Pls help ASAP

Using the reagents below, list in order (by letter, no period) those necessary to transform benzene into p-chlorobenzenesulfonic acid.
You may assume any undesired regioisomers can be separated.
Note: Not all spaces provided may be needed. Type "na" in any space where you have no reagent.
A.H₂, Pd
B.H2, Pd/CaSO4, quinoline M. SOCI₂
2
C. H₂, Ni₂B(P-2)
N. Br2, FeBr 3
D. Zn(Hg), HCI, reflux
O. Cl2, hv
E. i.O3, H₂O ii. Zn, H₂O
P. Cl2, FeCl3
F. MMPP, CH3CH₂OH
Q. H₂O
G. i. BH3; ii. H₂O2, NaOH
R. CH3CH₂CH₂CI, AICI 3
H.KOC(CH3)3, HOC(CH3)3
S. (CH3)3CCI, AICI3
Papa
L.HCI, peroxide

■ni
Kal
inc
I. HNO3, H₂SO4
J. SO3, H₂SO4
1
K. HCI, CH3CH₂OCH₂CH3 V.
Step #1
T. CH3 CH₂CH₂-C
2016-1
U. CH₂ CH₂
N
Step #2
CI
CI
CI
, AICI 3
, AICI 3
, AICI 3
ΝΑ
Step #3
ΝΑ
Step #4

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Step 1: Chlorination reaction of benzene

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Step 2: Chlorination reaction mechanism of benzene

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Step 3: Sulfonation reaction mechanism of chlorobenzene

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