1. (48 pts, 4 pts each) Give an acceptable IUPAC name for the following compound: CH)...
3. (16 pts, 4 pts each) Draw a structural formula for each of the following compounds that have a complex substituent. First interpret the name of the parent compound, then interpret the name of the substituent given in parentheses. By convention, the carbon atom of the substituent attached to the parent chain or ring is designated a. 4-(1,1-dimethylethyl)-4-octanol b. 3-chloro-2-(1-hydroxyethyl)-6-nitrophenol c. 3-2-fluoro-2.propenyl)-5-hepten-2-one d. 4-(1-methylethyl)-5-methyl-3-hexenal
Draw the structural formula for each of the following. (16 pts, 4 pts each) Draw a structural formula for each of the following compounds that have a complex substituent. First interpret the name of the parent compound, then interpret the name of the substituent given in parentheses. By convention, the carbon atom of the substituent attached to the parent chain or ring is designated C1. a. 4-(1,1-dimethylethyl)-4-octanol b. 3-chloro-2-(1-hydroxyethyl)-6-nitrophenol C. 3-(2-fluoro-2-propenyl)-5-hepten-2-one d. 4-(1-methylethyl)-5-methyl-3-hexenal
(4 pts) Ephedrine, shown below, is a potent dilator of air passages. The naturally occurring stereoisomer is levorotatory with an (a) of -41º. Assign R or S to each stereocenter. How many stereoisomers of Ephedrine are possible? H NHCH3 HOW TO 4 stereo isomers - (12 pts) Are the following pairs of drawings representing identical, enantiomeric or diastereomeric relationships? 9 R HC a Hobo oh Diastereomeric HCOH C- Id CH pe H Identical Hace Diastereomeria $ (16 pts, 4 pts...
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
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
(48 pts, 4 pts each) Give an acceptable IUPAC name for the following compounds 1. CH b. coH CH C. OH DO d. ollal ol oun COOH е. Br f. CH2 Br CH-CH,-CH-CH2-CH- CH,-CN
1. Give the IUPAC name for each of the following compounds. (2 pts each 8 pts total) OH ОН o que 2. Show the product and the mechanism for the following reaction (4 pts) [H) 2 тон
help with question #7 pts) 1. Give the IUPAC name for the following compound: NH OH H3 CH-CH2-CH-CH2-CH, D 5-amino-3-Hexanol amn 4 3 2 2 pts) 2. Draw the structural formula for 2-amino-3-oxo-pentanal. H-CH₂-CH₂-C- CH₂ - CH3 2 pts) 3. Write the balanced chemical equation (using structural formulas) for the lissociation of diethylamine in water. CH₃-CH₂-N-CH₂-CH₃ + H₂O -> CH₃-CH ₂ - N - CH₂ +OH-CH3 CAN- | CH-CH2N-CH, - Lidocaine (Xylocaine) 3 pts) 4. Lidocaine (Xylocaine) is used as...
1. Give the correct IUPAC name of the following compounds. (2 pts each) Name: 3-bromo benzoic acid çi Name: CH3CH2CH2CHCO-K+ © HOCCH2CHCOH Name: 2-methyl-1,4-branddie ce id CH3 NHCH3 Name: HN(CH3)3*CI- Name: CH3 CH3CHNHCH3 Name: 2. Draw the structural formula for the following compounds. (2 pts each) (a) 3-ethylpentanoic acid o Hok (b) methylammonium nitrate (c) cyclohexylamine (d) sodium o-methylbenzoate
Question 2 Give the chemical name of the following compounds. (12 pts) NH2 H CH 1) 2) OH c El . 3) 4 Page Section 01