12. Name the following compounds and draw the structure of the given name. (12 pts) Structure...
bond line structure of the following compounds on the lines 2. (5 pts.) Name or draw the bond line struc provided: a. (25, 6R)-cis-3-hepten-2,6-diol b. (hint: use R/ S nomenclature in the name) HO
Name or draw the following compounds. Please? Section 3: Nomenclature Name the following compounds using lUPAC nomenclature- or-provide the correct structure for the provided name. 32. 36. Br Cl 33. 5-fluoro-2-methylphenol 37. 34. 38. Ethyl 3-hydroxybutanoate 35. он 39. 4-hydroxy-4-methyl-2-pentanone
4.23 4.25 156 CHAPTER 4 Woction to Organic Compounds 4.27 Give the correct IUPAC name for each following compounds: b. Br Practice Problems 4.23 Draw the condensed structural formula for each of the following groups: a propyl bmethyl 4.24 Give the correct name for each of the following substituents: 2. CH.CH b. CH3CH-CH-CH- c.- 4.25 Draw the skeletal structure for each of the following compounds: a. 2,3-dimethylpentane b. 2-ethyl-1,4-dimethylcyclohexane c. 1,2-dichlorohexane 4.26 Draw the skeletal structure for each of the...
1. Please provide either the correct IUPAC name for the following compounds or the structure from the given IUPAC name. Pay attention to any stereochemistry N-phenyl-4-hydroxybutanamide Ethyl (R)-3-bromopentanoate
Can anyone name these 10-25? IUPAC WORKSHEET...continued Draw the structure for each of the following: (Show all hydrogens & their bonding as in EX 1.) 10. 3-methylhexane 11. 2.2-dimethylbutane 12. 3.propyinonane 13. 3-ethyl-4,4-dimethyldecane 14. 1.2-dimethylcyclohexane 15. 3-ethyl-1,1-dimethylcyclopentane Name the following: 16. CH3-CH2-CH=CH-CH 17. CH3-CRC-CH-CH3 CHE 18. CH3-CH-CH-CH2 ato . 19. CHo CH = CHO Draw the structure for each of the following: 22. 3-hexene 23. 3-ethylcyclooctene 24. 2-methyl-4-heptyne 25. 4,4,5-triméthyl-2-heptyna
PLEASE PROVIDE EXPLANATION 24. Draw the structures for 4 of the following 5 compounds. a. 4-(1,1-dimethylethyl)heptane b. 2,6-dimethyl-4-(2-methylpropyl)decane c. 1-bromo-4-(3,3,3-trifluoro-2-methylpropyl)-7-fluorooctane d. 6-ethyl-2,6,7-trimethyl-5-propylnonane e. 4-sec-butyl-1,2-dimethylcyclohexane 24. Draw the structures for 4 of the following 5 compounds. a. 4-(1,1-dimethylethyl)heptane b. 2,6-dimethyl-4-(2-methylpropyl)decane c. 1-bromo-4-(3,3,3-trifluoro-2-methylpropyl)-7-fluorooctane d. 6-ethyl-2,6,7-trimethyl-5-propylnonane e. 4-sec-butyl-1,2-dimethylcyclohexane
Review questions Name the following compounds. NAME: NAME: NAME: Draw a structure that corresponds with each name given below. 3-bromo-4-propylphenol 5-chloronona-2,5-dien-8-yne-2,7-diol 2-ethoxy-1-1-dimethylcyclobutane 2,4,6-trinitrotoluene Classify each of the following compounds as aromatic, antiaromatic, or nonaromatic. Assume planarity of the π network. To receive full credit, briefly explain your classification. Predict the major organic product of each of the following reactions.
2. Signature (8 p.) Draw the appropriate structure for each of the following compounds a) (S)-3-allylcyclobutene b) (R)-1.1.3-triiodocycloheptane c) 1,7,7-tribenzylbicyclo[2.2.1 heptane d) meso-4.7-decanediol 3. (9 pts.) Name the following compounds in an unambiguous manner (use an accepted common or L.U.P.A.C. me): Me-16-H Mets Mesh Ao T-methyl-4-phenyl bicyclo [2.2.0/nexane (R)-2-methyl-3-pentanol
Name the first two and draw the last two Cl 2. Draw the following compounds 1,3-dibromo-4-methylheptane 6-butyl-1-iodo-3-methyldecane
8. (a) Draw the structure of (4R,5R)-4-ethyl-5-fluoro-2-methyl heptane. Use solid and dashed wedges to show the proper configurations of the chiral centers. (0.4 pts) (b) Now draw a Newman projection for the most stable conformation of the C(4)-C(5) bond. (0.4 pts) H (c) Draw a diastereomer of (4R,5R)-4-ethyl-5-fluoro-2-methyl heptane (0.2 pts)