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Consider the following flowchart and table of compounds when answering questions 3 to 10 C, D,...
Please help I need to fill in the blanks by using the compounds and producers below the picture. Thanks! 422 (4 pts) Using the flow-chart below, outline a separation of Benzoic acid (s) (1), benzyl...
Please help I need to fill in the blanks by using the compounds
and producers below the picture. Thanks!
422 (4 pts) Using the flow-chart below, outline a separation of Benzoic acid (s) (1), benzyl amine d) (2), and Naphthalene (s) (3). From the list of procedural steps below, write the letter corresponding to each procedure in the appropriate Ellipse boxes. Each procedure ma once, more than once or not at all. Usi corresponding to each structure in the appropriate...
Experiment 3.5B Acid / Base Separations scheme worksheet Consider the following acid base separation scheme. Initialy,...
Experiment 3.5B Acid / Base Separations scheme worksheet Consider the following acid base separation scheme. Initialy, all compounds are dissolved in methylene chiloride and tne solution is extracted by 10% HCI . You will finish the extraction scheme with the following reagents: 10% HCI, 10% NaOH, Na SO Be sore to inclede the reagents and steps required so finish the estraction scheme. In the boses indicate which compounds (structures) are present in each layer after the extraction steps. (More than...
(10 poinis) What acyclic compound is formed when 6-hexanolactam is reacted with concentrated aqueous HC Hin...
(10 poinis) What acyclic compound is formed when 6-hexanolactam is reacted with concentrated aqueous HC Hin This is an amide hydrolysis reaction of a 7-membered ring lactam. Due to the acidic solution, does the product form as a salt (Y(N? (2) (10 points) What organic product is formed in the reaction of yndecanenitrile with aqueous base (NaOH. HO)? What organic product then forms when the reaction is subsequently acidified (HCI, H O)? Show both reactions
use this table to answer the following questions. Use this table to answer the following questions...
use this table to answer the following questions.
Use this table to answer the following questions in this week's exercise. Starting compounds Benzene Common reactions Nitration Toluene Sulfonation Redox reagents H2+ Pd-C, Fe+ HCl, or Sn+ HCI Zn(Hg) +HCI+, NH NH3 + 3H + KIMnO4, Na Cr 0; +H SO + H2O ZnO +1 Halogenation Friedel-Crafts alkylation Friedel-Crafts acylation NBS + hv Examples: This question is from the homework. What reaction(s)/reagent(s) do we use to prepare the prod What is...
11) (50 pts total) Consider the following 2 compounds: Yor You I II (a) (6 pts)...
11) (50 pts total) Consider the following 2 compounds: Yor You I II (a) (6 pts) Provide the IUPAC names for compounds I and II. Compound I: Compound II: (b) (10 pts) Draw the resonance contributors of compounds I and II. Which compound is more stable? Explain in 20 words or less. (c) (6 pts) Which C-N bond below is shorter, A or B ? Explain in 20 words or less. (d) (6 pts) Draw the products obtained when compound...
Organic Chem 142-01 2015 Dec 10 Name 6.Synthesis. Show how any THREE of the following compounds could be prepared, starting with benzene, toluene, cyclohexanol, or diethyl malonate, and any othe...
Organic Chem 142-01 2015 Dec 10 Name 6.Synthesis. Show how any THREE of the following compounds could be prepared, starting with benzene, toluene, cyclohexanol, or diethyl malonate, and any other necessary reagents. era mixture will give only the paroisomer) 18 points each CHO NHAc CO H оме Br NO2 7 of 9 Organic Chem 142-01 Name 2015 Dec 10 7. Write out THREE of the following reaction mechanisms. [10 points each] (a) Conversion of cyclopentanone to the oxime N-OH HCI...
Name: Date: Separation of Acid/Base/Neutral compounds using liquid-liquid extraction OCH CHO HN Benzocaine Molecular Weight: 165.19...
Name: Date: Separation of Acid/Base/Neutral compounds using liquid-liquid extraction OCH CHO HN Benzocaine Molecular Weight: 165.19 Melting Point: 88-90 °C 1,1-biphenyl Molecular Weight: 154.21 Melting Point: 68-70 °C trans-cinnamic acid Molecular Weight: 148.16 Melting Point: 132-135 °C Question 1: Identify the following compounds as Acid, Base or Neutral. (2 points) a. Benzocaine: b. Biphenyl: c. Trans-cinnamic acid: (2 points) _ (2 points) Question 2: Draw the structure in the box (5 points each): NaOH OCH,CH, HCM NaOHA HC form. Ples...
PLEASE ANSWER ALL QUESTIONS 23) How many distinct trichlorobenzene isomers are possible? A) 2 B) 3...
PLEASE ANSWER ALL QUESTIONS
23) How many distinct trichlorobenzene isomers are possible? A) 2 B) 3 C) 4 D) 5 E) 6 24) Which of the following is another accepted name for methylphenylketone? A) anisole B) cresol C) acetophenone D) benzophenone E) cresone 25) Provide the name of the compound shown below. 26) Provide an acceptable name for the compound below. NO, NO 27) Provide an acceptable name for PhSO3H. 28) Provide an acceptable name for the compound below. A)...
6. Which pair of the following compounds are constitutional isomers? A B and C B. A and D C. C and D D. B and D E....
6. Which pair of the following compounds are constitutional isomers? A B and C B. A and D C. C and D D. B and D E. A and C 7. Which pair of the following compounds are constitutional isomers? A B and C B. A and D C. C and D D. B and D E A and C 8. Which of the following is a Newman projection for the following compound as viewed down the indicated bond in...
C) E1 D) E2 E) E1cb 24. Rank is first, slowest is last) the following compounds...
C) E1 D) E2 E) E1cb 24. Rank is first, slowest is last) the following compounds in order of increasing reacdtivity in an a veaion Br Br IV 2. In the molecular orbital representation of benzene, how many T molecular orbitals are present? A) 1 B) 2 C) 4 D) 6 E) 8 26. What is the major difference between an antiaromatic and aromatic compound? A) The structure must be cyclic for aromatic but not antiaromatic compounds. B) Antiaromatic compounds...
Please help I need to fill in the blanks by using the compounds
and producers below the picture. Thanks!
422 (4 pts) Using the flow-chart below, outline a separation of Benzoic acid (s) (1), benzyl amine d) (2), and Naphthalene (s) (3). From the list of procedural steps below, write the letter corresponding to each procedure in the appropriate Ellipse boxes. Each procedure ma once, more than once or not at all. Usi corresponding to each structure in the appropriate...
Experiment 3.5B Acid / Base Separations scheme worksheet Consider the following acid base separation scheme. Initialy, all compounds are dissolved in methylene chiloride and tne solution is extracted by 10% HCI . You will finish the extraction scheme with the following reagents: 10% HCI, 10% NaOH, Na SO Be sore to inclede the reagents and steps required so finish the estraction scheme. In the boses indicate which compounds (structures) are present in each layer after the extraction steps. (More than...
(10 poinis) What acyclic compound is formed when 6-hexanolactam is reacted with concentrated aqueous HC Hin This is an amide hydrolysis reaction of a 7-membered ring lactam. Due to the acidic solution, does the product form as a salt (Y(N? (2) (10 points) What organic product is formed in the reaction of yndecanenitrile with aqueous base (NaOH. HO)? What organic product then forms when the reaction is subsequently acidified (HCI, H O)? Show both reactions
use this table to answer the following questions.
Use this table to answer the following questions in this week's exercise. Starting compounds Benzene Common reactions Nitration Toluene Sulfonation Redox reagents H2+ Pd-C, Fe+ HCl, or Sn+ HCI Zn(Hg) +HCI+, NH NH3 + 3H + KIMnO4, Na Cr 0; +H SO + H2O ZnO +1 Halogenation Friedel-Crafts alkylation Friedel-Crafts acylation NBS + hv Examples: This question is from the homework. What reaction(s)/reagent(s) do we use to prepare the prod What is...
11) (50 pts total) Consider the following 2 compounds: Yor You I II (a) (6 pts) Provide the IUPAC names for compounds I and II. Compound I: Compound II: (b) (10 pts) Draw the resonance contributors of compounds I and II. Which compound is more stable? Explain in 20 words or less. (c) (6 pts) Which C-N bond below is shorter, A or B ? Explain in 20 words or less. (d) (6 pts) Draw the products obtained when compound...
Organic Chem 142-01 2015 Dec 10 Name 6.Synthesis. Show how any THREE of the following compounds could be prepared, starting with benzene, toluene, cyclohexanol, or diethyl malonate, and any other necessary reagents. era mixture will give only the paroisomer) 18 points each CHO NHAc CO H оме Br NO2 7 of 9 Organic Chem 142-01 Name 2015 Dec 10 7. Write out THREE of the following reaction mechanisms. [10 points each] (a) Conversion of cyclopentanone to the oxime N-OH HCI...
Name: Date: Separation of Acid/Base/Neutral compounds using liquid-liquid extraction OCH CHO HN Benzocaine Molecular Weight: 165.19 Melting Point: 88-90 °C 1,1-biphenyl Molecular Weight: 154.21 Melting Point: 68-70 °C trans-cinnamic acid Molecular Weight: 148.16 Melting Point: 132-135 °C Question 1: Identify the following compounds as Acid, Base or Neutral. (2 points) a. Benzocaine: b. Biphenyl: c. Trans-cinnamic acid: (2 points) _ (2 points) Question 2: Draw the structure in the box (5 points each): NaOH OCH,CH, HCM NaOHA HC form. Ples...
PLEASE ANSWER ALL QUESTIONS
23) How many distinct trichlorobenzene isomers are possible? A) 2 B) 3 C) 4 D) 5 E) 6 24) Which of the following is another accepted name for methylphenylketone? A) anisole B) cresol C) acetophenone D) benzophenone E) cresone 25) Provide the name of the compound shown below. 26) Provide an acceptable name for the compound below. NO, NO 27) Provide an acceptable name for PhSO3H. 28) Provide an acceptable name for the compound below. A)...
6. Which pair of the following compounds are constitutional isomers? A B and C B. A and D C. C and D D. B and D E. A and C 7. Which pair of the following compounds are constitutional isomers? A B and C B. A and D C. C and D D. B and D E A and C 8. Which of the following is a Newman projection for the following compound as viewed down the indicated bond in...
C) E1 D) E2 E) E1cb 24. Rank is first, slowest is last) the following compounds in order of increasing reacdtivity in an a veaion Br Br IV 2. In the molecular orbital representation of benzene, how many T molecular orbitals are present? A) 1 B) 2 C) 4 D) 6 E) 8 26. What is the major difference between an antiaromatic and aromatic compound? A) The structure must be cyclic for aromatic but not antiaromatic compounds. B) Antiaromatic compounds...
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