Draw the structure of each compound
Draw the structure of each compound 1. Draw the structure of each compound: (a) cis-1,2-Cyclohexanediol (b)...
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
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
acid catalyzed hydration of 1 methylcyclohexene yields 2 alcohols. The major product does not undergo oxidation, while the minor product will undergo oxidation, explain. 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 the reagents you would use to accomplish each of the following transformations: DH (4) tage...
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
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.
QUESTIONS 1. Select a reagent that will distinguish between each pair of compound Write equations for any reactions that occur. The reagent should react ONLY with one compound of the pair under reaction conditions. Reagent (1) l-propanol zincill 2-propanol OH Equation(s) (2) 2-butanol 2-roethyl-2-propanol (3) 1-propanol 1-chloropropane Popu (4) 1-propanol propene - (5) 2-pentanol 3-pentanol 2. Number the alcohols below according to increasing boiling points. Recall that addition of -CH - usually increases the boiling point by anout thirty degrees...
HELP What is the common UPAC name for the following compound? 1 нс b) 1-methyl-3-cyclohexene d) 1-methyl-4-cyclohexene a) 5 methylcyclohexene c 4 methylcyclohexene Methylcyclohexene e) Which of the following is capable of exhibiting cis-trans isomerism? a) 1-pentene 2. b) 1-butene c) 2- pentene d) Cyclohexene e) Ethene What is the relationship between the following compounds: 3. Н,с a) Conformational isomers b) Constitutional isomers c) Configurational isomer d) Structural isomers e) Positional isomers Which of the following is the most stable...