From the table of reagents shown below, show how you synthesize the product from the given reactant.BrReagents availablea. NBS, (PhCO2)2 h. CH3 Cl, AIC13CUCN0.b. Br2, FeBr3i. CH3 CH2 Brр. НзО*, дс. Вг2, Н+j. CH3O¯, Aq. CH; CH2 COCI, AICI3r.k. CH3 COCI, AICI3H2NNH2,OH, Ad. OH-e. NaOH(s), A1. Mg, Et20s. H2, Pd/Cf. HNO3, H,SO4m. CO2(s) then H3O+ t. H3PO2g. H2 CrO4n. HONO 0°Cu. Cl2, FeCl3(Enter the letter(s) of the reagent(s) needed in the box, in the order that they must be used. No more than two steps are required toperform the synthesis. Note that a retrosynthetic arrow is used, and therefore the reactant is shown on the right.)Answer:

Benzene ring is brominated using Br2 and a Lewis acid catalyst. The reaction proceeds through an…

From the table of reagents shown below, show how you synthesize the product from the given reactant. Br Reagents available a. NBS, (PhCO2)2 h. CH3 Cl, AlCl3 CUCN 0. b. Br2, FeBr3 i. CH3 CH2Br p. H3O", A c. Br2, H+ j. CH3O¯, A q. CH3 CH2COCI, AICI3 r. H2NNH2, OH,A d. OH k. CH3 COCI, AIC13 e. NaOH(s), A 1. Mg, Et20 s. H2, Pа/C f. HNO3, H2 SO4 m. CO2(s) then H3O* t. H3PO2 g. H2 CrO4 n. HONO 0°C u. Cl2, FeCl3 (Enter the letter(s) of the reagent(s) needed in the box, in the order that they must be used. No more than two steps are required to perform the synthesis. Note that a retrosynthetic arrow is used, and therefore the reactant is shown on the right.) Answer:

From the table of reagents shown below, show how you synthesize the product from the given reactant. Br Reagents available a. NBS, (PhCO2)2 h. CH3 Cl, AlCl3 CUCN 0. b. Br2, FeBr3 i. CH3 CH2Br p. H3O", A c. Br2, H+ j. CH3O¯, A q. CH3 CH2COCI, AICI3 r. H2NNH2, OH,A d. OH k. CH3 COCI, AIC13 e. NaOH(s), A 1. Mg, Et20 s. H2, Pа/C f. HNO3, H2 SO4 m. CO2(s) then H3O* t. H3PO2 g. H2 CrO4 n. HONO 0°C u. Cl2, FeCl3 (Enter the letter(s) of the reagent(s) needed in the box, in the order that they must be used. No more than two steps are required to perform the synthesis. Note that a retrosynthetic arrow is used, and therefore the reactant is shown on the right.) Answer:

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...

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