The target molecule above can be prepared by treating benzene with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. CH₂CH₂COCI, AICI D (CH3)₂CHCI, AICI B HNO3, H₂SO4 E Cl₂, AICI 1) CH3CH₂COMgBr 2) H₂O* F 1) (CH₂)₂CHMgBr 2) H₂O

The target molecule above can be prepared by treating benzene with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. CH₂CH₂COCI, AICI D (CH3)₂CHCI, AICI B HNO3, H₂SO4 E Cl₂, AICI 1) CH3CH₂COMgBr 2) H₂O* F 1) (CH₂)₂CHMgBr 2) H₂O

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter19: Aldehydes And Ketones: Nucleophilic Addition Reactions

Section19.SE: Something Extra

Problem 28VC

See similar textbooks

Similar questions

Starting with benzene and using any other reagents of your choice, design a synthesis for the following compound: Br XX O₂N The target molecule above can be prepared by treating benzene with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. A HNO3, H₂SO4 D Fuming H₂SO4 B E Br2, AlBr3 Dilute H₂SO4 C BrMg F MgBr axxa. AICI 3
Starting with benzene and using any other reagents of your choice, design a synthesis for the following compound: OEt CI & NO₂ The target molecule above can be prepared by treating benzene with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. A 1) EtMgBr 2) H₂O¹ D NaOEt, heat B HNO₂, H₂SO4 E NaOH, heat C D F Cl₂, AICI CH-CH₂COCI, AICI
Starting with benzene and using any other reagents of your choice, design a synthesis for the following compound: The target molecule above can be prepared by treating benzene with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. A OEt 1) EtMgBr 2) H₂O* D NaOEt, heat B HNO3, H₂SO4 E NaOH, heat с F Cl₂, AICI3 CH3CH₂COCI, AICI
Write a mechanism that accounts for the formation of ethyl isopropyl ether as one of the products in the following reaction. CI OEt HCI EtOH Write the mechanism for step one of this reaction. Show lone pairs and formal charges. Only the acidic hydrogen should be drawn out with a covalent bond. Write the mechanism for step two of this reaction (where the product of step one reacts with the solvent, ethanol). Show lone pairs and formal charges. Only the acidic hydrogen should be drawn out with a covalent bond. Write the mechanism for the last step of this reaction (formation of ethyl isopropyl ether). Show lone pairs and formal charges. Only the acidic hydrogen should be drawn out with a covalent bond. CI will act as the base in this reaction.
Starting with benzene and using any other reagents of your choice, design a synthesis for the following compound: OEL CI 13 NO₂ The target molecule above can be prepared by treating benzene with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. HNO3, H₂SO4 A 1) EtMgBr 2) HjO B C Cl₂, AICI D E F NaOEt, heat NaOH, heat CH3CH2COCI, AICI
. Please provide a forward synthesis for the following aromatic compounds using benzene as the starting material for all of your syntheses. In some cases, you might run a reaction that produces two products. This outcome is fine; just draw both products, and indicate that you will separate them, and then proceed forward with the compound needed. Br HO2C, Br CI
IF esize this compound by the → t-butyl ethyl ether Show the steps necessary to synthesize this compound by a rignard reaction. Start with an alkyl halide; after that you can add any organic or inorganic compound. → 1-hexanol Consider the following compounds:
Provide reagents/conditions to accomplish the following syntheses. Several steps are required in some cases. H2N NH2 Но TH. NH2 HO
Starting with benzene and using any other reagents of your choice, design a synthesis for the following compound: CI * Incorrect. COOH A Br The target molecule above can be prepared by treating benzene with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. ECABF D NO₂ 1) KMnO4, NaOH, heat 2) H3O+ HNO3, H₂SO4 B E 1) CO2 2) H3O+ (CH3)2CHCI, AICI 3 с Br2, AlBr3 F Cl2, AICI 3
Write the products of the following sequences of reactions. Refer to your reaction roadmaps to see how the combined reactions allow you to navigate between the different functional groups. Note that you will need your old Chapters 611, Chapters 1518, and Chapter 19 roadmaps along with your new Chapter 20 reaction roadmap for these.
Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated , -unsaturated isomers. Propose a mechanism for this isomerization.
Following is the structural formula of the tranquilizer meparfynol (Oblivon). Propose a synthesis for this compound starting with acetylene and a ketone. (Notice the -yn- and -ol in the chemical name of this compound, indicating that it contains alkyne and hydroxyl functional groups.)