Select all the following statements that are correct.1BrBr2Br34BrCompound 1 will react faster than Compound 3 in the Nal/2-butanone reactivitytest.Compound 1 will be the fastest to react with Nal/2-butanone because it is aprimary alkyl halide.Compound 4 will be the fastest to react with Nal/2-butanone because it is ahighly substituted alkyl halide.Compound 2 will be the fastest to react with Nal/2-butanone because it is atertiary alkyl halide.Compound 2 will react faster than Compound 3 in the Nal/2-butanone reactivitytest.

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Answered: Select all the following statements…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter21: Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions

Section21.SE: Something Extra

Problem 54AP: The following reactivity order has been found for the saponification of alkyl acetates by aqueous...

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Choose the right reagent or series of reagents from the ones listed below to prepare 2-pentanone from acetylene. NaNH2NaNH2 followed by CH3CH2CH2BrCH3CH2CH2Br, then disiamylborane followed by H2O2H2O2, HO−HO− H2H2, Lindlar followed by H2OH2O, H+H+ NaNH2NaNH2 and CH3CH2CHOCH3CH2CHO NaNH2NaNH2 followed by H2OH2O, H+H+ NaNH2NaNH2 followed by CH3CH2CH2BrCH3CH2CH2Br, then H2OH2O, H2SO4H2SO4, HgSO4 Choose one.
Which of the following starting materials and reagents would be best to produce a racemic mixture of 3-methyl-3-hexanol? heptanone and 1. CH3MgBr 2. H3O+ hexanal and 1. CH3MgBr, 2. H3O+ 3-hexanone and 1. CH3MgBr, 2. H3O+ butanal and 1. CH3CH2MgBr, 2. H3O+
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How would you synthesize the following compounds from cyclohexanone using reagents from the table? Use letters from the table to list reagents in the order used (first at the left). Reagents a 1. CH3MgBr/dry ether 2 H3O+ e 1. OsO4 i 1. BH3/THF 2. NaHSO3/H2O 2. H₂O₂ / NaOH b 1. C6H5MgBr / dry ether f 1. NaBH4 j Mg / dry ether 2 H3O+ 2. H3O+ с PBr3 g HOCH2CH2OH/HCI k H2/Pd d m-chloroperbenzoic h H3O+ / heat I CrO3 / H3O+ acid m cyclohexanone a) cyclohexylbenzene b) 2-phenylcyclohexanone Submit Answer Try Another Version 3 item attempts remaining
How would you synthesize the following compounds from cyclohexanone using reagents from the table? Use letters from the table to list reagents in the order used (first at the left). Reagents a 1. CH3MgBr / dry ether 2 H3O+ e 1. OsO4 i 1. BH3/THF 2. NaHSO3/H₂O 2. H₂O₂ / NaOH b 1. C6H5 MgBr / dry ether f 1. NaBH4 j Mg / dry ether 2 H3O+ 2. H3O+ C PBг3 g HOCH2CH2OH/HCI k H2/Pd d m-chloroperbenzoic h H3O+ / heat 1 CrO3 / H3O+ acid a) 2-phenylcyclohexanone b) cyclohexylbenzene m cyclohexanone
Treatment of acetylene with a suitable base affords lithium acetylide, which was used as a reagent in a partial synthesis of the antitumor natural product (+)-acutiphycin. (Org. Lett. 2014, 16, 1168-1171) Possible bases to consider H-C=C-H Acetylene Step 1 Li :Base T H-O: Li Lithium hydroxide (LiOH) three steps Lithium acetylide Draw the structure of lithium acetylide. Draw Your Solution di. Η Η Η Η | | | | H-C-C-C-C: II HH HH Butyllithium (BuLi) OR CEC- Li OH CH3 -H CH3 Lithium diisopropyl amide (LDA) OMe H3C H H₂C many steps Li HO OH I (+)-Acutiphycin CH3 CH₂ "OH
What is the best choice of reagent to achieve the following reaction? ? H2/Pd NaOH, H₂O H2SO4 K2Cr2O7, H2SO4 CH3 + CH3CH2OH
Please don't provide handwritten solution
show the missing reagents and intermediates in the reaction sequence below
Question 13 Propose best Williamson ether syntheses for the following compounds. Select all applicable options (multiple answers can be possible). Note: Some compounds cannot be made using Williamson synthesis reaction. ΚΗ A: + ⚫OH ΕΘ OK SN2 KH ΘΘ + -Br B: -OH OK SN1 C: ☐ A B ☐ C Cannot be synthesized using Williamson ether syntheses.
Show the reagents for the conversion below: OMe

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