What reagents are suitable to carry out the conversion shown? HO Br HO (A) 1. (CH3)3SICI / (CH3CH2)3N; 2. Mg/ether; 3. i 4. H2O; 5. TBAF (B) 1. (CH3)3SICI / (CH3CH2)3N; 2. ; 2. H2O; 4. TBAF 1. (CH3)3SICI/(CH3CH2)3N; 2. Mg/ether; 3. ; 4. H2O (D) 1. (CH3)3SICI / (CH3CH2)3N; 2. Mg/ether; 3. (E) 1. (CH3)3SICI / (CH3CH2)3N; 2. Mg; 3. ; 4. H2O; 5. TBAF H H ; 4. H2O H H OH

What reagents are suitable to carry out the conversion shown? HO Br HO (A) 1. (CH3)3SICI / (CH3CH2)3N; 2. Mg/ether; 3. i 4. H2O; 5. TBAF (B) 1. (CH3)3SICI / (CH3CH2)3N; 2. ; 2. H2O; 4. TBAF 1. (CH3)3SICI/(CH3CH2)3N; 2. Mg/ether; 3. ; 4. H2O (D) 1. (CH3)3SICI / (CH3CH2)3N; 2. Mg/ether; 3. (E) 1. (CH3)3SICI / (CH3CH2)3N; 2. Mg; 3. ; 4. H2O; 5. TBAF H H ; 4. H2O H H OH

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...

See similar textbooks

Similar questions

Which set of reagents would be appropriate to synthesize bromobenzene from benzene? O 1. HNO3 in H2SO4; 2. H2CrO4 and heat O 1. H2CrO4 and heat; 2. H2 Pd/C O Br2 and FeBr3 O 1. CH3CH2CHCI and AICI3; 2. H2CRO4 and heat O4B12 and Fe O Heat and Br2 OBR2, HCI
Provide the reagents necessary to carry out the following conversion. A) 1. CH3CH₂C/AICI3; 2. Cl₂/FeCl3; 3. KMnO4, H₂O, heat B) 1. CH3CH₂CI/AICI3; 2. (CH3)₂CHOH/AICI³Cl₂/FeCl³; 3. 3. H₂O, heat O CH₂CH₂Cc C) 1. (CH3)2CHCI/AICI3; 2.; CH3CH₂CCI/AICI3 3. Zn(Hg)/HCI, heat 1 CH₂CH₂CC₁/ D) 1 CH3CH₂CCI / AICI 3 2. CH3CH₂CI/AICI3; 3. Zn(Hg)/HCI, heat
select 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
(a) 2-methyl-2-pentanol Draw the structure of the alkene that was used to prepare the alcohol in highest yield. AAVIL ? ChemDoodleⓇ Which process does this employ? 1. Hg(OAc)2, H₂O; 2. NaBH4 01. BH3; 2. H₂O2, NaOH OsO4, H₂O2 On n [ ]#
H3C H C=C CH3 H m-chloroperoxybenzoic acid CH2Cl2, rt C-C--. H3CH2CC H H3C CH3 Cl₂ H₂O NaOH H₂O D. S- E. CH3 H₂O₂, H₂O It CH₂O Na + CHI F. HI, H₂O heat G. 4 OH CH3CHCH3 + ICH2CH3 1. NaH (CH3)3COH (CH3)3 COCHCH2CH3 2. CH3
What reagents are necessary to carry out the conversion shown? O O Br O MgBr; Mg/ether; CrO3, H₂SO4; O 1. Mg/ether; 2. H O LIAIH; H3O+; PCC/CH₂Cl2 O ; H30¹; PCC/CH₂Cl₂ H ; H3O+; PCC/CH₂Cl₂ O O O H CI ; H3O+ ; 3. H30; 4. AICI 3
Which of the following would accomplish the transformation below? a) 1. HSCH2CH2SH, H+; 2. H2, Raney Ni b) H2N-NH2, NaOH(aq), heat c) H2, Pd d) All of the above
ll mobily ? 4:13 PM O 21% O < Homework - carboxylic a... CH3CHCH2CH2CHCH3 CH3CCO2H CH3 (c) .CO2H (d) CH3 CH3CCN CH3 (g) Br (h) CN BRCH2CHCH2CH2CO2H Q2: Draw structures corresponding to the following IUPAC names: (a) cis-1,2-Cyclohexanedicarboxylic acid (b) Heptanedioic acid (c) 2-Hexen-4-ynoic acid (d) 4-Ethyl-2-propyloctanoic acid (e) 2-Cyclobutenecarbonitrile Q3: How could you convert butanoic acid into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert each of the following compounds into butanoic acid? Write each step showing all reagents. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert butanenitrile into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) Butylamine
H3C OH OH CH3 1,3-pentanediol + B OMe OME OME MeO... CH3 H3C OMe benzaldehyde dimethylacetal catalytic Me 0:0 OH FO (p-TsOH) CH3CN H... MeO, OMe OMe e a & H3C CH3 H3C CH3 H3C CH3 C D A HO E HO OCH3
Draw the products formed when ethylene oxide is treated with each reagent. a. HBr b. H2O(H2SO4) c. [1] CH3CH2O; [2] H2O d. [1] HC ≡ C−; [2] H2O e. [1] −OH; [2] H2O f. [1] CH3S−; [2] H2O
O (1) H20, H*; (2) Jones reagent (1) H20, H*; (2) PCC, CH2CI2 (1) conc. H2SO4: (2) Jones reagent O (1) H20, H*; (2) Tollens reagent (1) conc. H2SO4: (2) PCC, CH2CI2 O (1) conc. H2SO4: (2) Tollens reagent
None