bond line structure of the following compounds on the lines 2. (5 pts.) Name or draw...
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
1) 2-amino-3-hydroxybutanoic acid 2) 2,3-dinitrobutane A. Draw the skeletal structure (line-bond) for the following compounds. B. Convert the structures to the Most Stable and the Least Stable Newmann projections around (looking down) C2-C3 bond. (The numbering is based on the nomenclature locator numbers) C. On your skeletal structures, label the stereogenic centers (chiral carbons) if there are any. D. Draw all the possible stereoisomers for the compounds. Indicate which are enantiomer pairs. which are diastereomers to each other, and if...
Question 1: Provide the systematic name or draw the bond-line structure for the following compounds: CH3 Нас CH c) 4,4-dimethyl-2-pentyne
2. Draw structure (or) name the molecules according to IUPAC rules. (10 pt) i. 2,6-dimethyl-5-propyloctane Name the following compounds according to IUPAC nomenclature. ii. E: CH.CH C(CH3) 3. Give five different structures of CH3 alkyl groups, and identify the carbon at the point of attachment as primary, secondary or tertiary as appropriate. (10 pt)
12. Name the following compounds and draw the structure of the given name. (12 pts) Structure Name c) (4R,8S)-4-iodo-2.2,8- trimethyldecane d) (R)-2-ethyl-1.1- dimethylcyclohexane
1.) 2-amino-3-hydroxybutanoic acid 2.) 2,3-dinitrobutane A. Draw the skeletal structure (line-bond) for the following compounds. B. Convert the structures to the Most Stable and the Least Stable Newmann projections around (looking down) C2-C3 bond. (The numbering is based on the nomenclature locator numbers) C. On your skeletal structures, label the stereogenic centers (chiral carbons) if there are any. D. Draw all the possible stereoisomers for the compounds. Indicate which are enantiomer pairs. which are diastereomers to each other, and if...
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.
draw a structure for the following compounds compounds: Draw a structure for the following 14-(1,1-Dimethylethyl) – 4-octanal <3 - Chloro-2-(4-hydroxyethyl) -6- nitrophenol ③ 3-(2-Fluoro-2-ProPenyl)-5-hepten-2-one 6 4-(1-methylethyl)-5-methyl-3-hexanal
ох 1. Provide the name of the following compounds. så stk 2. Provide the name of the following compounds. 3. Provide the line structure given the following names. A. 2,6,6,8-tetramethyl-5-neopentyldecane R. 7-methylbicycln[4.2.2]decane ох 4. A. Draw the Newman Projection of pentane looking down the C2-C3 bond in a stageered confirmation B. Draw an energy diagram showing the conformational analysis using the Newman Projection above (showing a 360 degree total rotation, 60 degrees at a time). Hint - see Figure 46,...
Write the IUPAC name for each of the compounds drawn below on the line provided. Be sure to include stereochemical information if applicable (R, S, Cis, Trans, E, Z) Instructions: write the IUPAC name for each of the compounds drawn below on the line provided. Be sure to include stereochemical information if applicable (R, S, cis, trans, E, Z) CI Cl Br Instructions: write the IUPAC name for each of the compounds drawn below on the line provided. Be sure...