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5. Fill in the table below with the results you expect for the following alcohols. Test...
5. in the below with the results you pect for the towing alcohol Compound 1 Compound...
5. in the below with the results you pect for the towing alcohol Compound 1 Compound OH Structure Classification Solubility in HD Oxidation Test: CrO, Ferric Chloride Test: Feci. 11-12 Experiment 11 Alcohols and Phenols
Alcohols and PHUVIL Report Sheet D. Ferric Chloride Test Alcohol FeCl, Test Ethanol 2-propanol 1-Butyl alcohol Cycl...
Alcohols and PHUVIL Report Sheet D. Ferric Chloride Test Alcohol FeCl, Test Ethanol 2-propanol 1-Butyl alcohol Cyclohexanol Phenol Unknown E. Identification of Unknown Substance Unknown # Conclusions Results Summary of Testing B. Odor B. Soluble in water? B.PH C. Oxidation: CO 2 D. FeCl3 Structure Name of Unknown Page 8 of
2. Name the following alcoholis. ame: Cyclpentah Structure: Name: Structure: ОН CH, CH,CH,C- OH CH Name:...
2. Name the following alcoholis. ame: Cyclpentah Structure: Name: Structure: ОН CH, CH,CH,C- OH CH Name: Name: Structure: Structure: ОН Сн, он CH, -CH-CH2-CH, CH-CH, CH3 3. Write the product of the following oxidation reactions (if no reaction, write NR). CH, OH CH3-CH-CH, CH, CH-CH, +(0) — лон +(0) - Ketone CH, OH CH3 CH, CH, CH-CH-CH-CH, +(0) -OH + (0) 11-10 Experiment 11 Alcohols and Phenols Post-Lab Questions 1. Write the structures and classifications of the following alcohols: 2-bromo-3-pentanol...
1. How would you interpret results if the chromic acid test gave a blue-green color quickly AND t...
1. How would you interpret results if the chromic acid test gave a blue-green color quickly AND the iron (III) test gave a purple color? 2. Draw the mechanisms for the oxidation of 2-propanol in chromic acid and phenol in FeCl3 solution as performed above. 3. Which compound will oxidize faster in FeCl3 solution, 4-nitrophenol or 4-aminophenol? Explain your answer. 4. What are the products from the oxidation of the following alcohols by Jones' reagent (CrO3 in 50% sulfuric acid)?...
What products would you expect from oxidation of the following alcohols? (Figure 1) Figure (< 1...
What products would you expect from oxidation of the following alcohols? (Figure 1) Figure (< 1 of 1 > OH (b) CH,CHCH2CH2CH3 (a) CH3CH2CH2OH OH | (CCHCH, CH
Background: Oxidation of Alcohols is the removal of two hydrogens from the reaction site. Tertiary alcohols...
Background: Oxidation of Alcohols is the removal of two hydrogens from the reaction site. Tertiary alcohols are unable to undergo oxidation because they do not have two hydrogens in the reaction site. Oxidation of carbonyl families such as aldehydes and ketones is the addition of oxygen to the reaction site. In order to add oxygen to the reaction site a terminal hydrogen needs to be bonded to a primary carbonyl carbon. Ketones cannot undergo oxidation because they have a secondary...
Pre-lab: If your unknown was 2-bromooctanoic acid, what would you expect the results of the following...
Pre-lab: If your unknown was 2-bromooctanoic acid, what would you expect the results of the following tests to be? Solubility in: H2O NaOH NaHCO3 HCl H2SO4 Jones Oxidation Test: 2,4-DNP Test: Flame Test: Beilstein Test:
Q.2 In your textbook or a chemistry handbook, look up and draw the condensed structural formulas...
Q.2 In your textbook or a chemistry handbook, look up and draw the condensed structural formulas and uses of thymol, menthol, and resorcinol. Circle the phenol functional group in each structure. If the compounds are available in lab, carefully note and describe their odors. B. Properties of Alcohols and Phenol and C. Ferric Chloride Test Odor pH FeCl, Test Ethanol 2-propanol t-Butyl alcohol Cyclohexanol Phenol Unknown Report Sheet Alcohols and Phenols D. Oxidation of Alcohols Alcohol D.4 D.1 Color Change...
Alcohols, Aldehydes, and Ketones Report Sheet Q.5 Indicate the test results for each of the following...
Alcohols, Aldehydes, and Ketones Report Sheet Q.5 Indicate the test results for each of the following compounds in the iodoform test and in the Benedict's test: lodoform Test Benedict's Test CH.CCH.CH CH,CH CH3CH2CCH,CH, 0 0 CH3CCH.CH Q.6 Two compounds, A and B have the formula of C3H,0. Determine their condensed structural formulas and names using the following test results. a. Compound A forms a red-orange precipitate with Benedict's reagent, but does not react with iodoform. b. Compound B forms a...
Please answer 2 through 5 2) Fill in the reaction table below. Make sure you correctly...
Please answer 2 through 5
2) Fill in the reaction table below. Make sure you correctly calculate the molar amounts (mol.-eq.) of your reactive materials name ormulamol.-eq mo ensi romobenzend C6H5Br | magnesium Mg C13H10 70 0.15 g 1.09 g HCI (6M) HC -6.0 m product H 3) Calculate the theoretical yield of your product, i.e. the mass you would expect to recover (assuming 100% conversion to product). Show your work. 4)Grignard reactions are particularly sensitive to water, and are...
5. in the below with the results you pect for the towing alcohol Compound 1 Compound OH Structure Classification Solubility in HD Oxidation Test: CrO, Ferric Chloride Test: Feci. 11-12 Experiment 11 Alcohols and Phenols
Alcohols and PHUVIL Report Sheet D. Ferric Chloride Test Alcohol FeCl, Test Ethanol 2-propanol 1-Butyl alcohol Cyclohexanol Phenol Unknown E. Identification of Unknown Substance Unknown # Conclusions Results Summary of Testing B. Odor B. Soluble in water? B.PH C. Oxidation: CO 2 D. FeCl3 Structure Name of Unknown Page 8 of
2. Name the following alcoholis. ame: Cyclpentah Structure: Name: Structure: ОН CH, CH,CH,C- OH CH Name: Name: Structure: Structure: ОН Сн, он CH, -CH-CH2-CH, CH-CH, CH3 3. Write the product of the following oxidation reactions (if no reaction, write NR). CH, OH CH3-CH-CH, CH, CH-CH, +(0) — лон +(0) - Ketone CH, OH CH3 CH, CH, CH-CH-CH-CH, +(0) -OH + (0) 11-10 Experiment 11 Alcohols and Phenols Post-Lab Questions 1. Write the structures and classifications of the following alcohols: 2-bromo-3-pentanol...
What products would you expect from oxidation of the following alcohols? (Figure 1) Figure (< 1 of 1 > OH (b) CH,CHCH2CH2CH3 (a) CH3CH2CH2OH OH | (CCHCH, CH
Background: Oxidation of Alcohols is the removal of two hydrogens from the reaction site. Tertiary alcohols are unable to undergo oxidation because they do not have two hydrogens in the reaction site. Oxidation of carbonyl families such as aldehydes and ketones is the addition of oxygen to the reaction site. In order to add oxygen to the reaction site a terminal hydrogen needs to be bonded to a primary carbonyl carbon. Ketones cannot undergo oxidation because they have a secondary...
Q.2 In your textbook or a chemistry handbook, look up and draw the condensed structural formulas and uses of thymol, menthol, and resorcinol. Circle the phenol functional group in each structure. If the compounds are available in lab, carefully note and describe their odors. B. Properties of Alcohols and Phenol and C. Ferric Chloride Test Odor pH FeCl, Test Ethanol 2-propanol t-Butyl alcohol Cyclohexanol Phenol Unknown Report Sheet Alcohols and Phenols D. Oxidation of Alcohols Alcohol D.4 D.1 Color Change...
Alcohols, Aldehydes, and Ketones Report Sheet Q.5 Indicate the test results for each of the following compounds in the iodoform test and in the Benedict's test: lodoform Test Benedict's Test CH.CCH.CH CH,CH CH3CH2CCH,CH, 0 0 CH3CCH.CH Q.6 Two compounds, A and B have the formula of C3H,0. Determine their condensed structural formulas and names using the following test results. a. Compound A forms a red-orange precipitate with Benedict's reagent, but does not react with iodoform. b. Compound B forms a...
Please answer 2 through 5
2) Fill in the reaction table below. Make sure you correctly calculate the molar amounts (mol.-eq.) of your reactive materials name ormulamol.-eq mo ensi romobenzend C6H5Br | magnesium Mg C13H10 70 0.15 g 1.09 g HCI (6M) HC -6.0 m product H 3) Calculate the theoretical yield of your product, i.e. the mass you would expect to recover (assuming 100% conversion to product). Show your work. 4)Grignard reactions are particularly sensitive to water, and are...
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