Specify the reagent(s) suitable for converting 3-ethyl-4-methyl-2-pentene to 2-bromo-3-ethyl-4-methylpentane. Check all that apply. NaBr ☑ ⑤ Peroxyacetic acid Br₂ HBr BH3 Peroxides H₂ None of the above
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- The following series of reaction steps will yield __________. 1) But-1-yne plus NaNH2; 2) the product of Step 1 plus Butanone; 3) followed by H3O+ 3-methyl-hept-4-yne-3-ol formic acid, propanal and butan-2-ol an octane-based compound containing both a ketone and an alkyne CO2, propanoic acid and buta-1,2-dione 4-methyl-hept-4-yne-1-olHW9 #516 eBook Print References 3 attempts left Check my work Specify reagents suitable for converting 3-ethyl-2-pentene to 3-ethyl-3-pentanol. Select the single best answer. O H₂, Pt HCI H₂O, H₂SO4 peroxyacetic acid 1. B₂H6; 2. H₂O₂, HO™
- From the table of available reagents select the one(s) you would use to convert: 3-pentanol to 3-bromopentane. 3-pentanol to 3-methylpentane. Use the minimum number of steps; in no case are more than four steps necessary. List reagents by letter in the order that they are used; example: fa. Reagents available а. ВН3, ТHF; then H2O2, OH f. Н2, Pd b. Br2 g. Mg c. CH3MgBr; then H30+ h. NABH4; then H3O+ d. i. PB13 CrO3, H, SO4, H20 e. CH2=0; then H3O+ j. POC1 , pyridineA student wanted to try to make phenoxyacetic acid using hydroxyacetic acid (HOCH2COOH) and chlorobenzene. His plan was to use NaH to deprotonate both OH groups, and then the more basic alkoxy group would react with the chlorobenzene. Would this procedure work? Explain.Question 14 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. Br ΚΗ A: LOH 00 OK SN2 Br NaH 00 B: OH ONa SN2 C: Cannot be synthesized using Williamson ether syntheses. □ A B C
- please help and thank youHW9 #2This question has multiple parts. Work all the parts to get the most points. meta-Chloroperoxybenzoic acid (m-CPBA) is not the only peroxy acid capable of reacting with alkenes to form epoxides. For the reaction below: H3C H3C CH₂ + CF3CO3H a Draw the structure of the major organic product derived from the alkene. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Use wedge and hash bonds ONLY when needed to show reaction stereochemistry. . If the reaction produces a racemic mixture, just draw one stereoisomer. 3*2 c C -> O 000 - IF
- 15 eBook Print References 3 attempts left Check my work Specify reagents suitable for converting 3-ethyl-2-pentene to 2,3-dibromo-3-ethylpentane. Select the single best answer. HBr, peroxides NaBr, acetone Br2, CC14 1. B₂H6; 2. H₂O₂, HO™ HBr17 eBook Print References Specify reagents suitable for converting 3-ethyl-2-pentene to 2,3-epoxy-3-ethylpentane. Select the single best answer. peroxyacetic acid 1. B₂H6; 2. H₂O2, HO™ 3 attempts left Check my work O H₂O, H₂SO4 Cr₂0₂², H 03, CH3OHA lab technician planned to synthesize 2-bromopentane using 2-pentanol, heat, and HBr. However, the labtechnician did not have HBr in the lab. What other reagent(s) can the technician use to synthesize 2-bromopentane using 2-pentanol as the starting material?