Ofa/?tstamp3D1651674579 PART 1: TRUE OR FALSE. Choose A If the statement is true. Otherwise, choose D. 1. The carbocation of n-propyl alcohol is more stable than the carbocation of isopropyl alcohol. 2. The C-0-C bonds in ether have a higher bond dipole than the C-0-H bond in alcohol. 3. When n-propyl alcohol undergoes an elimination reaction, the resulting product is an alkene. 4. As the alkyl chain increases in molecular weight among primary alcohol, the solubility in water increases. 5. An ethoxide ion exhibits greater proton-accepting property compared to an ethyloxonium ion. 5. Phenol is more acidic than cyclohexyl alcohol due to the electron-donating ability of phenolic oxygen. 7. When isopropyl alcohol reacts with HCI, the resulting product is 2-chloropropane. B. Nucleophilic molecules are electron-rich molecules that can "attack" electron-deficient molecules. 9. Based on the physical property, hydroquinone has a lower boiling point compared to catechol. 10. When FeCla is used in visualizing aspirin in thin layer chromatography, the resulting spot is red in color. 11. The solubility of monocarboxylic acid in water increases as the alkyl chain increases in length. 12. The resulting iodinated aspirin has a higher Rf compared to aspirin after visualizing with ferric chloride. 13. Substitution reactions do not occur in aromatic rings because of pi-electron delocalization. 14. Chlorination of phenol occurs even if the reagent AICIa is missing. 15. The molecule 2,4,6-trinitrophenol, being a phenolic compound, tests positive for the FeCl: test. PART 2: MULTIRLE CHOICE
Ofa/?tstamp3D1651674579 PART 1: TRUE OR FALSE. Choose A If the statement is true. Otherwise, choose D. 1. The carbocation of n-propyl alcohol is more stable than the carbocation of isopropyl alcohol. 2. The C-0-C bonds in ether have a higher bond dipole than the C-0-H bond in alcohol. 3. When n-propyl alcohol undergoes an elimination reaction, the resulting product is an alkene. 4. As the alkyl chain increases in molecular weight among primary alcohol, the solubility in water increases. 5. An ethoxide ion exhibits greater proton-accepting property compared to an ethyloxonium ion. 5. Phenol is more acidic than cyclohexyl alcohol due to the electron-donating ability of phenolic oxygen. 7. When isopropyl alcohol reacts with HCI, the resulting product is 2-chloropropane. B. Nucleophilic molecules are electron-rich molecules that can "attack" electron-deficient molecules. 9. Based on the physical property, hydroquinone has a lower boiling point compared to catechol. 10. When FeCla is used in visualizing aspirin in thin layer chromatography, the resulting spot is red in color. 11. The solubility of monocarboxylic acid in water increases as the alkyl chain increases in length. 12. The resulting iodinated aspirin has a higher Rf compared to aspirin after visualizing with ferric chloride. 13. Substitution reactions do not occur in aromatic rings because of pi-electron delocalization. 14. Chlorination of phenol occurs even if the reagent AICIa is missing. 15. The molecule 2,4,6-trinitrophenol, being a phenolic compound, tests positive for the FeCl: test. PART 2: MULTIRLE CHOICE
Chemistry for Today: General, Organic, and Biochemistry
9th Edition
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Chapter13: Alcohols, Phenols, And Ethers
Section: Chapter Questions
Problem 13.14E: Classify the following alcohols as primary, secondary, or tertiary: a. b.CH3CH2CH2CH2OH c.
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