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(3 pts each, unless otherwise noted, 16 pts total) 1-5. Nomenclature: provide an acceptable name for...
(3 pts each, unless otherwise noted, 16 pts total) 1-5. Nomenclature: provide an acceptable name for each of the following molecules, but do NOT Google. 1. 2. 3 H2N CO H H-C-N(CH)2 CO, NA (7 pts) 4. НО. CH3 N H CHE
(3 pts each, unless otherwise noted, 17 pts total) 1-5. Nomenclature: provide an acceptable name for each of the following compounds, but do NOT Google. 1. 2. 3. -CO No HN -CO,H COM 5. (5 pts) Name IUPAC ONLY. i HN-CHE H-C-N(CH)2 (4 pts each, unless otherwise noted, 16 pts total) 6-9. Structures: provide an acceptable structure for: 6. the isobutyl diester of B-bromopimelic acid (5 pts) 7. N-ethyl-B-ethyl-y-valerylactam. 8. benzoic B-chloropropionic anhydride (3 pts) 9. o-bromobenzoyl chloride
Need help with #5-8 (5 pts each, unless otherwise noted, 19 pts total) 5-8. Structures: provide an acceptable structure for: (4 pts) 5. the sec-butyl monoester of B-bromopimelic acid 6. N-methyl-B-isopropyl-5-valerolactam 7. a-chloropropionic ß-aminobutyric anhydride NH2 Br- 8. ethylisopropylmethylpropylammonium bromide
(4 pts each, unless otherwise noted, 47 pts total) 9-17. Syntheses: draw / provide the likely organic product(s) generated in each of the reactions (or reaction sequences) below. As appropriate, pay attention to regiospecificity (new bond formation and location in the product formed) and stereochemistry (direction in space of new bond(s) formed). Indicate ALL likely products; where one product does not predominate, label / indicate the MAJOR product(s). Where a product mix results, indicate the MINOR or TRACE product(s). (12...
(4 pts each, unless otherwise noted, 45 pts total) 10-18. Syntheses: draw / provide the likely organic product(s) generated in each of the reactions (or reaction sequences) below. As appropriate, pay attention to regiospecificity (new bond formation and location in the product formed) and stereochemistry (direction in space of new bond(s) formed). Indicate ALL likely products: where one product does not predominate, label / indicate the MAJOR or predominant product(s). Where a product mix results, indicate the MINOR or TRACE...
CH3 но SH 1. Name the following thiol using IUPAC nomenclature (5 pts). 2. Name the following organometallic compound according to IUPAC nomenclature (5 pts) CH CH:CHa) CuLi 3. Write the product of the following reaction while carefully considering the underlying mechanism (5 pts) 1. LiAID4, Et20 2. H20 4. Complete the following retrosynthetic scheme and while applying an organometallic reaction (5 pts). CH3 CH H3
please provide nomenclature for a through j. thanks! Nomenclature Provide the IUPAC name for the following a. CHỊCH-CH(CH3)CH2CH(CHO)CH, C. (CH3)3CCH2C(CH3)3 d. C(CH3)4 f. CH3C(CI)2CH(CH3)2 h. (CH2CH2)2CHCH(CH3)CH2CH3 j. CH2CH(CH3)CCCH2CH3
12. (5 pts) Nomenclature: Provide the systematic IUPAC name for each of the following molecules. Indicate stereochemistry if applicable (R,S). CI
18. (15 pts) Nomenclature: Provide the systematic IUPAC name for each of the following molecules. Indicate stereochemistry if applicable (Cis, Trans). 19. (6 pts) Draw all constitutional isomers of C&H Brz.
Provide the structure(s) of the expected major organic product(s). Unless mentioned otherwise, you can assume that all reagents are present in one mole. Show stereochemistry where needed and write NR if there is no reaction. + NH2 CO2H 2 moles NaOH H2N N + H NH3 CH2CH(CH3)2 ОН bia H2N