1. Draw the structure of each compound: (a) cis-1,2-Cyclohexanediol (b) Isobutanol (c) 2,4,6-Trinitrophenol (d) (R)-2,2-Dimethyl-3-heptanol (e)...
1. Draw the structure of each compound: (a) cis-1,2-Cyclohexanediol (b) Isobutanol (c) 2,4,6-Trinitrophenol (d) (R)-2,2-Dimethyl-3-heptanol (e) Ethylene glycol (f) (S)-2-Methyl-1-butanol
1. Draw the structure of each compound: (a) cis-1,2-Cyclohexanediol (b) Isobutanol (c) 2,4,6-Trinitrophenol (d) (R)-2,2-Dimethyl-3-heptanol (e) Ethylene glycol (f) (S)-2-Methyl-1-butanol
1. Draw the structure of each compound: (a) cis-1,2-Cyclohexanediol (b) Isobutanol (c) 2,4,6-Trinitrophenol (d) (R)-2,2-Dimethyl-3-heptanol (e) Ethylene glycol (f) (S)-2-Methyl-1-butanol
1. Draw the structure of each compound: (a) cis-1.2-Cyclohexanediol (b) Isobutanol (C) 2,4,6-Trinitrophenol (d) (R)-2,2-Dimethyl-3-heptanol (e) Ethylene glycol (1) (S)-2-Methyl-1-butanol
Draw the structure of each compound 1. Draw the structure of each compound: (a) cis-1,2-Cyclohexanediol (b) Isobutanol (c) 2,4,6-Trinitrophenol (d) (R)-2,2-Dimethyl-3-heptanol (e) Ethylene glycol (0) (s)-2-Methyl-1-butanol 2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol. Show a mechanism for this reaction 3. Acid-catalyzed hydration of 1-methylcyclohexene yields two alcohols. The major product does not undergo oxidation, while the minor product will undergo oxidation. Explain. 4. Using 2-propanol as your only source of carbon, show how you would prepare 2-methyl- 2-pentanol. 5. Identify...
2. Draw the structures of the cis-trans isomers for each compound. Label them cis and trans. If no cis-trans isomers exist, write none. a. 2,3-dimethyl-2-pentene b. 1,1-dimethyl-2-ethylcyclopropane c. 1,2-dimethylcyclohexane d. 5-methyl-2-hexene e. 1,2,3-trimethylcyclopropane
Draw a structural formula for each compound: (a) 1-Isopropyl-4-methylcyclohexene (b) (6E)-2,6-Dimethyl-2,6-octadiene (c) trans-1,2-Diisopropylcyclopropane Note: use wedged and dashed bonds to show stereochemistry. (d) 2-Methyl-3-hexyne (e) 2-Chloropropene (f) Tetrachloroethylene
2. Draw structures corresponding to the following IUPAC names a. 2-methy-1,J-hexadiene b. (Z)-3-ethyl-2,2-dimethyl-3-heptene a. Z-me c. 3.4-diisopropyl-2,5-dimethyl-3-hexene d. (E)-5-methyl-4-hepten-2-ol
4. Draw structures corresponding to the following systematic names; a) 1-isopropyl-4-methylcyclohexene b) 3-butyl-2-heptene c) 4-methyl-1,2- hexadiene d) trans-3,3-dimethyl-4-propyl-1,5-octadiene e) (42)-2,4-diethyl-1,4-hexadiene f) 1.2-propadiene g) (32,5E) -2,6-dimethyl-1,3,5,7-octatetraene h) cis-2,2,5,5-tetramethyl-3-hexene i) Methylenecyclohexane, j) trans- 1,2 divinylcyclohexane
A 4-Isopropyl-1,1-dimethyl-1 penal B S-Isopropyl-1.1-dimethyl-2-hexal 1.1.4.5-Tetramethyl-1-hexanol D 3.5.6-Trimethyl-3-heptanol E 2,5,6-Trimethyl-2-heptanol 9. A chemist attempted unsuccessfully to form iodoethane from ethanol using Nal. Why did the reaction fail? A. I was not a good enough nucleophile. B. A secondary or tertiary alcohol was needed. C O H is a poor leaving group. D. Na was a poor counterion. following cardo ving carbonyl compounds does not give 2-methylpentan-2-o ther followed by a workup with aqu