### Question:From the table of reagents shown below, show how you synthesize the product from the given reactant.#### Chemical Reaction:- **Reactant:** An aromatic ring with a bromine atom at the benzylic position and a ketone at the para position.- **Product:** An aromatic ring with a ketone group at the para position without the bromine atom.#### Reagents Available:| Reagent Code | Reagent Description ||--------------|-----------------------------|| a. | NBS, (PhCO₂)₂ || b. | Br₂, FeBr₃ || c. | Br₂, H⁺ || d. | OH⁻ || e. | NaOH(s), Δ || f. | HNO₃, H₂SO₄ || g. | H₂CrO₄ || h. | CH₃Cl, AlCl₃ || i. | CH₃CH₂Br || j. | CH₃O⁻, Δ || k. | CH₃COCl, AlCl₃ || l. | Mg, Et₂O || m. | CO₂(s) then H₃O⁺ || n. | HONO 0°C || o. | CuCN || p. | H₃O⁺, Δ || q. | CH₃CH₂COCl, AlCl₃ || r. | H₂NNH₂, OH⁻, Δ || s. | H₂, Pd/C || t. | H₃PO₂ || u. | Cl₂, FeCl₃ |#### Instructions: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: [ ]**

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:

Chemistry

10th Edition

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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