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(3 pts each, unless otherwise noted, 17 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, 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
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...
NOMENCLATURE: Choose the correct IUPAC name for each of the structures below. If the correc name doesn't appear, choose "none of the above." (3 pts each) a. 2-butyl-2-methylepoxide b. 1,2-epoxy-2-methylbutane c.2-butyl-2-methyloxirane d. 1,2-epoxy-2-methylpropane e. none of the above a. 1-ethoxy-2-isopropyl ether b. ethyl isobutyl ether c. 1-ethyl-2-methylbutane d. 1-ethoxy-2-isobutyl ether e. none of the above 3. I a. 1-sec-butyl-2-methylcyclopentene b. 1-iso-butyl-2-methylcyclopentane c. 1-methyl-2-sec-butylcyclopentene d. 1-sec-butyl-2-methylcyclohexene e, none of the above 4. Provide the structure for pyridine in the box below:...
12. (5 pts) Nomenclature: Provide the systematic IUPAC name for each of the following molecules. Indicate stereochemistry if applicable (R,S). CI
(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...
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.
1) Draw the structure for each named compound: a) (Z)-N-ethyl-3-bromo-2-isopropyl-5- b) propanoyl chloride methyl-2-hexenamide c) benzoic anhydride d) (R)-3-chloro-4-ethylhexanoic acid e) ethyl 4-methylpentanoate f) pentanenitrile g) cyclohexanecarboxamide h) octyl butanoate 2) Provide an IUPAC name for each structure: b) 9 CH d) CH.CH нс снсон TH Page
1. Nomenclature and stereochemistry: Provide Name or Structure (3 pts cach) a) (2S,3S)-2-bromo-3-fluoro-pentane b) cis- 1-cyclobutyl-3-isopropyl-cyclopentane d) Br f) Butyl acetate g) 3,3-difluoro-2-propyl-hexanoic acid h) Methyl ethyl ketone i) N,N-diethylamide