ze COOH 2. (36 pts, 4 pts each) Draw a structure for the following compounds: a....
Чно CH,-CH,-CH-CH,-CH-C,-CN Br HOOD "р но Сно. н'о "ю 1. (48 pts, 4 pts each) Give an acceptable IUPAC name for the following compounds: Y'A CH h. он i. сно k. СООН Br NO2 2. (36 pts, 4 pts each) Draw a structure for the following compounds: a. 2-amino-2-methylbutanol b. 4-hexynol
1. (48 pts, 4 pts each) Give an acceptable IUPAC name for the following compound: CH) i 0 CO,H CH, OH Font Font COOH CH,_ch, bi-ch, bi-CH, CN CH OH CHO Font соон NO 2. (36 pts, 4 pts each) Draw a structure for the following compounds: a. 2-Amino-2-methylbutanol b. 4-Hexynol C. 3-Methoxycycloheptanecarboxylic acid d. 2-Phenylethanol e. 3-Hydroxycyclopentanecarboxamide f. 4-Bromobenzaldehyde Font g. 6-Bromohexanoic acid h. 2, 3, 4-Hexanetriol L1-Decanthi 3. (16 pts, 4 pts each) Draw a structural formula for...
Name and draw following benzene derivatives 4. Name or Draw the following compounds: COOH COOH 1. p-carboxybenzenesul fonic acid C(CH3)3 3. mmethoxyanisole 4. 3,4-dimethoxybenzaldyde OCH3 5. H2N OCH3
JI) Name the compounds or draw the structures from their names. (2 pts) 1,2-chovo mul COOH a) NO2 b) CI c) 4-phenyl-2-pentanol; •DH d) 1-bromo-2-chloro-4-ethylbenzene; 2. Arrange the compounds in each set in order of decreasing reactivity (fastest to slowest) toward EAS. Explain. (2 pts) 0-C-CH3 -C-0-CH3 a) (A) (B) (C) CH2CH3 -NH2 ( C1) do nosotros (B) b) (A) 3. Account for the observation that trifluoromethyl groups is meta directing, as shown in the following example. (1 pt) CF3...
Draw the starting materials (diene and dienophile) for the preparation of the following compounds. COOH COOH
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
52. Arrange the relative pKa's of the following compounds:( P (2 pts) соон соон COOH pKa's: 53. Arrange th compounds: (2 pts) e relative reaction rates for the electrophilic aromatic substitution of the following CH3 OCHa NO2 Reaction rates: 54. Arrange the relative base strength of the following compounds: (2 pts) NHCOCH3 NH2 NH2 NH2 NH. OCH3 OCH3 Basicity 55. What is the splitting pattern for the labeled hydrogens in the following compounds? (5 pt CH CH 56. Provide one...
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
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
Draw the structure of following compounds 3. Draw the structure of following compounds. 4-Bromo 3- chlorobenzoic acid 4-Chlorobutyl-3-chloro hexanoate Isobutyl acetate MacBook Air esc F1 F2 20 F $ 4 2 3 % 5 & 7 6 & Pentandjoic acid Cyclo propane dicarboxylic aad MacBook Air F2 F3 FS 97 # $