7. Pick two of the following compounds, and provide a synthetic scheme to produce the following compounds starting from benzene, using any inorganic material, and any organic material with 4 carbons or less. If you have produced a compound, you can use that compound in subsequent work without showing its synthesis again. NH2 H,C. CH, OH NH2 CH3 CH, CH, a) b) H3CO d) H,C

7. Pick two of the following compounds, and provide a synthetic scheme to produce the following compounds starting from benzene, using any inorganic material, and any organic material with 4 carbons or less. If you have produced a compound, you can use that compound in subsequent work without showing its synthesis again. NH2 H,C. CH, OH NH2 CH3 CH, CH, a) b) H3CO d) H,C

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter9: Nucleophilic Substitution And Β-elimination

Section: Chapter Questions

Problem 9.45P: Draw a structural formula for the major organic product of each reaction and specify the most likely...

See similar textbooks

Similar questions

14)Synthesize the molecule below from reagent and inorganic precursors. H₂C-0 H₂C .CH3 CH3 H₂C A O CH3 CH3 , methanol, an appropriate Grignard
7. Pick two of the following compounds, and provide a synthetic scheme to produce the following compounds starting from benzene, using any inorganic material, and any organic material with 4 carbons or less. If you have produced a compound, you can use that compound in subsequent work without showing its synthesis again. NH2 H;C. CH3 ОН NH2 CH3 CH3 CH3 а) b)_ H3CO d) H,C-
SYNTHESIS Synthesize (2) two of the following compounds using cyclohexanol, or any organic reagent that has 4 or fewer carbons, and any common reagents d. CH3 С. но, е.
Synthesize the following compound from cyclohexanone and any other organic compound and provided reagents. 1) (CH3); CuLi (1) Br2, CH300H (1) CH3B1 C. A. В. (2) H20 (2) Li¿CO2, LiBr, DMF (2) H20 heat NaOEt, E1OH D. OH, H20 E. (1) CH3CI, DMF F. CH2(CN)2 (2) H30" Part 1 out of 3 edit structure .. Organic compound
D. Compound KILUA can be synthesized from benzene using four steps. Show the most plausible reaction sequence that will yield KILUA from benzene using the given pool of reagents. O2N. COOH CI KILUA Available reagents: (a) Hot acidic KMNO4 (b) Cl2, UV light (c) fuming H2SO4 (d) HNO3, H2SO4 (e) CH3CH2CI, AICI3 (f) CH3COCI, AICI3 (g) Cl2, FeCl3 (h) Cl2, H20 (i) N2OH Reaction Sequence: O2N СООН CI
4 Starting from benzene, devise a synthesis for the following compounds. a. b. C. d. & مهم Br CH3 NO₂ NO₂ OH Oc-CH, 'Br
2a) (2 ) Provide the reagents or products for the following reactions. Include ALL stereochemistry, where appropriate. i). ii) iii) Z-4-octene CHO 1) MCPBA/DCM 2) H₂O* NaOCH, CH,OH .CO.I heat ol NH₂ OH
Provide the structure of the major organic product which results in the following reactions. Br (CH:)3CO Br2 1.(xs)NANH2 H&SO4 CCI4 2.H2O H2SO4 CH3
Ethers/Aldehydes/Ketones SynthesisPrepare the following compounds from any simple alkyl halide having four carbons or less,cyclohexane, and/or benzene. You may also use ethylene oxide (oxacyclopropane). SHOW ALLSTEPS AND REAGENTS with arrows.
Which set of reagents would be appropriate to synthesize bromobenzene from benzene? 1. HNO3 in H2SO4; 2. H2Cr04 and heat 1. H2CrO4 and heat; 2. H2 Pd/C Br2 and FeBr3 1. CH3CH2CHCI and AICI3; 2. H204 and heat 4B12 and Fe Heat and Br2 Br2, HCI
3. Naphthalene undergoes electrophilic substitution at the a-position. Predict the organic products of the monosubstitution reactions of naphthalene with each of the following sets of Ha H reagents. a) Br2, FeBr3 b) HNO3, H2SO4 c) CICH₂CH3, AlCl3 d) (CH3)2CHOH, H₂SO4 e) CI-C- " AICI3 H. H H H H H В
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