Which compound will produce an alkyl iodide via an SN2 mechanism? Select one: a. 1 b. Il c. III d. IV I CH3CH₂OH + 10 II + CH3CH₂OH2 III (CH3)3COH IV (CH3)3COH + Select one: O al O b. ll O c. III O d. IV 10 show work of all options.don't give Ai generated solution
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- Select the best reagents for the reaction below. O 1. OsO4; 2. NaHSO3, H₂O O 1. Hg(OAc)2, H₂O; 2. NaBH4 O 1. RCO3H; 2. H3O+ O H₂SO4, HO O 1. 03: 2. DMS OH OH + enantiomerDraw the main products B-C of each of the following reactionsIdentify the best reagents to complete the following reaction. I HO O A B C D E LIAIH4 DMP (Dess-Martin Periodinane) mCPBA 1. KMnO4, NaOH 2. Neutralizing work-up PCC
- hw34Identify the best reagents to complete the following reaction. 1 HO 8 A B O D E LIAIH4 DMP (Dess-Martin Periodinane) mCPBA 1. KMnO4, NaOH 2. Neutralizing work-up PCC W Submit 110:10 AM Mon Nov 27 2 of 2 a. b. OH CH3 i) H₂SO4 (CH3)3COCH₂CH₂CH3 HBr (2 eq) H 0.84 c) d) tert-butoxide + iodopropoane → e) 1-bromopentane + sodium benzenethiolate → upvisayas.net CH₂Cl₂ solvent f. What products can be formed when each alcohol: OH OH OH 1. Is dehydrated with H₂SO4? (Identify the major and minor product if any). 2 Is oxidized with Ka @ 95%
- Suggest the mechanism for each reaction (consider stereochemical aspects when necessary). a. b. C. CH3 1.H₂C=CHMgBr 2. H₂O CHO CH3 NaCN HCI (CH3)2NH mild acid ? ? NUCLEOPHILIC ADDITION ?with detail mechanism plzselect reagents: cyclopentanone Reagents a. C6H5CHO b. NaOH, ethanol c. Pyrrolidine, cat. Hj. d. H₂C=CHCN e. H3O+ f. LDA g. A) bg EtOC(=O)CO₂Et h. i. B) ka k. I. m. O: BrCH₂CH=CH₂ NatOEt, ethanol Br₂, H+ K+ t-BUO™ CH2(CO2Et)z heat C) jh CO₂Et D) Im
- NoneSelect an appropriate synthetic route of the diol shown starting with 1,1,3,3-tetramethyl-2-ethylcyclohexane. OH ОН + enantiomer 1. Br2, hv; 2. KOtBu; 3. HBr, ROOR; 4. KOtBu; 5. Br₂; 6. xs NaNH2; 7. CH3Br; 8. H₂, Lindlar's catalyst; 9. RCO3H; 10. H3O+ O 1. Br2, hv; 2. KOtBu; 3. HBr, ROOR; 4. KOtBu; 5. Br₂; 6. xs NaNH2; 7. CH3Br; 8. H₂, Pt; 9. OsO4, NMO; 10. NaHSO3, H₂O 1. Br2, hv; 2. KOtBu; 3. HBr, ROOR; 4. KOtBu; 5. Br₂; 6. 1 equiv. NaNH2; 7. CH3Br; 8. H₂, Lindlar's catalyst; 9. OsO4; 10. H3O+ O 1. Br2, hv; 2. KOtBu; 3. HBr, ROOR; 4. KOtBu; 5. Br₂; 6. xs NaNH2; 7. CH3Br; 8. H₂, Lindlar's catalyst; 9. OsO4, NMO; 10. NaHSO3, H₂O O 1. Br2, hv; 2. KOtBu; 3. HBr, ROOR; 4. KOtBu; 5. Br₂; 6. xs NaNH2; 7. CH3Br; 8. H2, Pd; 9. RCO3H; 10. H3O+Which alkene cannot be converted into an alkyl bromide with HBr, ROOR, hv, A? III IV A. B. C. D. E. All react Which synthetic route is best to give the major product shown below. ? x XA OH A. 1. BH3; 2. H₂O2, NaOH; 3. HBr; 4. CH3CO₂H B. 1. Br₂, 2. NaCCH; H₂, Lindlar's; 3. O3; 4. H₂O C. 1. NBS, hv, A; 2. H₂, Pd; 3. NaO₂CCH3 D. 1. NBS, hv, A; 2. NaCCH; 3. H₂2, Pd; 4. O3; 5. H₂O E. 1. NBS, hv, A; 2. H₂, Pd; 3. NaCCH; 4. 03; 5. H₂O Which synthetic route is best for the transformation shown below? OH ? OH A. 1. H₂SO4/heat; 2. HgOAC2, H₂O; 3. NaBH4 B. 1. HBr; 2. NaOH, DMSO C. 1. TsCl, pyr; 2. NaOH, DMSO D. 1. TsCl, pyr; 2. KOtBu; 3. BH3-THF; 4. H₂O2, NaOH E. 1. H₂SO4/heat; 2. BH3-THF; 3. H₂O2, NaOH =B