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QUESTION What is the major product of the following reaction? 8R...
What is the major organie product obtained from the following reaction-2 (dute) CH LCH, OH CH...
What is the major organie product obtained from the following reaction-2 (dute) CH LCH, OH CH OM 1 QUESTION 28 Which of the following best describes the reaction of sodium metal with methanol to give hydrogen and sodium methoxide? Lewis acid-base Bransted Lowry acid-base electrophile-nucleophile oxidation-reduction QUESTION 29 Which of the following reagents would be best for oxidizing a 10-alcohol to an aldehyde? H3PO4 PCC Jones' reagent (H2C:04) OsO4 Click Save and Submit to save and submit. Click Save All...
12. Which is the major product of the reaction shown? (a) (b) (c) (d) 13. What...
12. Which is the major product of the reaction shown? (a) (b)
(c) (d) 13. What are all of the possible products formed in the
following reaction? (choose all correct answers) (a) (b) (c) (d)
(e) (f) 14. The three compounds below can form a carbocation in the
presence of H2O and H2SO4. Which ones will form the same
carbocation? (a) I and II (b) I and III (c) II and III (d) all
three will form the same carbocation...
4. Explain things in the following question(s) In each reaction, identify the Brønsted-Lowry acid, the Brønsted-Lowry...
4. Explain things in the following question(s) In each reaction, identify the Brønsted-Lowry acid, the Brønsted-Lowry base, the conjugate acid, and the conjugate base. (a) H2SO4(aq) + H2O(l) —— HSO4 (aq) + H30+(aq) (b) HCO3(aq) + H20(1) = H,CO3(aq) + OH(aq) 5. Using examples, distinguish between a Nucleophile vs Electrophile. Give at least 2 differences between the 2 concepts 6. What are curved arrows or "curly arrows" in Organic Chemistry? What do they represent? Give an example (b) Using Ammonia...
Question completion What will be the major product from the following reaction sequent OVE HD -...
Question completion What will be the major product from the following reaction sequent OVE HD - C. OH 1 2 000 QUESTION 33 What product(s) are expected from the following reaction! HI (excess 2 2 CH3CH21 2 ICH3CH2OH 2 ICH2CH2 CH3CH2 - CH2CH2OH QUESTION 34 From the data given in the right-hand box, what is the specific rotation, [ap of the alcohol produced in the SN2 reaction shown below? Data H OH H "OH CeHCHCH Cohio "Celio lalo =-34.6 BrCH,...
please answer all of the following questions. 1. [03 pts. For the following reaction, label the...
please answer all of the following questions.
1. [03 pts. For the following reaction, label the nucleophile, electrophile, and leaving group. nucleophile" Lexleasing group 2. [03 pts. Rank the following substrates from most to least reactive in an S2 reaction. 3. [02 pts.) Which of the following is the reaction diagram for endothermic Sn2 reaction? Xo 4. [03 pts.] Draw the major product for the following Sn2 reaction. NaCN 5. [02 pts.) Which reaction in the following pair takes place...
PLEASE ONLY ANSWER FIRST QUESTION Consider the following reaction: Cd2+ (aq) + 4CN (aq) +- Cd(CN)2- (aq) In this partic...
PLEASE ONLY ANSWER FIRST QUESTION
Consider the following reaction: Cd2+ (aq) + 4CN (aq) +- Cd(CN)2- (aq) In this particular reaction CN is acing as a 1. Bronsted Lowry acid 2. Bronsted Lowry base 3. Lewis acid 4. Lewis base 5. Both a and c 6. Both b and d QUESTION 5 The solubility of Zinc hydroxide, Zn(OH)2, in water when dilute nitric acid is added to it? 1. Increases 2. First decreases, then increases 3. Does not change 4....
please i need quick help these questions are due so soon and i dont know the answers please help me thanks . Que...
please i need quick help these questions are due so soon and i
dont know the answers please help me thanks .
Question Completion Status: QUESTION Consider the following acid-base reaction. Equilibrium for this reaction lies to the: OH H-CEC + H-CEC-H + A. right. B. Equilibrium favors neither forward nor reverse reaction. O C. left. D. It cannot be determined. QUESTION 2 Does the equilibrium of this reaction lie to the left or right? BF OH BF3 + A,...
Please answer all 3 questions QUESTION 32 What is the product from the acid-catalyzed addition of...
Please answer all 3 questions
QUESTION 32 What is the product from the acid-catalyzed addition of methanol to 22-diethylomirane? CH3OHH 3,3-dimethoxypentane 2-ethyl-1-methoxy-1-butanol 2-ethyl-1-methoxy-2-butanol 2-ethyl-2-methoxy-1-butanol QUESTION 33 What are the products when the following triol is treated with H104? Оно 1 OH OH HIO4 OH 0 0 0 0 w N- QUESTION 34 In which of these Lewis structures would the sulfur be assigned a formal charge of +1? 30 CH-S-0 CH-5-03 CH3-5-C1 CH3-5-CE 2
Question 5 (4 points) What is the major product of the following reaction? 1. NaOET Eto...
Question 5 (4 points) What is the major product of the following reaction? 1. NaOET Eto ΟΕΙ 2. Hot O OE EIO OH OE O O- EIO OH OEt OE EtO 애 OEt Question 6 (4 points) Friedel-Crafts acylation reactions cannot be performed on benzoic acid because: The carboxylic acid group gets acylated instead of the aromatic ring. The carboxylic acid group is moderately deactivating preventing any substitution on the aromatic ring. The carboxylic acid group attacks the Lewis acid...
Help on all parts of question 3 would be greatly appreciated! 3. Treating alkene "A" below...
Help on all parts of question 3 would be greatly
appreciated!
3. Treating alkene "A" below with HBr can lead to a number of products. "A" + H-Br A bunch of products. For real, hella products. 3.A. Label the stereocenters in compound "A" as R or S and label the alkene as E or Z. 3.B. Draw the curved arrow mechanism leading to the most stabilized carbo- cation intermediate. (don't do any rearrangements, just acid/base with the alkene) H-Br most...
What is the major organie product obtained from the following reaction-2 (dute) CH LCH, OH CH OM 1 QUESTION 28 Which of the following best describes the reaction of sodium metal with methanol to give hydrogen and sodium methoxide? Lewis acid-base Bransted Lowry acid-base electrophile-nucleophile oxidation-reduction QUESTION 29 Which of the following reagents would be best for oxidizing a 10-alcohol to an aldehyde? H3PO4 PCC Jones' reagent (H2C:04) OsO4 Click Save and Submit to save and submit. Click Save All...
12. Which is the major product of the reaction shown? (a) (b)
(c) (d) 13. What are all of the possible products formed in the
following reaction? (choose all correct answers) (a) (b) (c) (d)
(e) (f) 14. The three compounds below can form a carbocation in the
presence of H2O and H2SO4. Which ones will form the same
carbocation? (a) I and II (b) I and III (c) II and III (d) all
three will form the same carbocation...
4. Explain things in the following question(s) In each reaction, identify the Brønsted-Lowry acid, the Brønsted-Lowry base, the conjugate acid, and the conjugate base. (a) H2SO4(aq) + H2O(l) —— HSO4 (aq) + H30+(aq) (b) HCO3(aq) + H20(1) = H,CO3(aq) + OH(aq) 5. Using examples, distinguish between a Nucleophile vs Electrophile. Give at least 2 differences between the 2 concepts 6. What are curved arrows or "curly arrows" in Organic Chemistry? What do they represent? Give an example (b) Using Ammonia...
Question completion What will be the major product from the following reaction sequent OVE HD - C. OH 1 2 000 QUESTION 33 What product(s) are expected from the following reaction! HI (excess 2 2 CH3CH21 2 ICH3CH2OH 2 ICH2CH2 CH3CH2 - CH2CH2OH QUESTION 34 From the data given in the right-hand box, what is the specific rotation, [ap of the alcohol produced in the SN2 reaction shown below? Data H OH H "OH CeHCHCH Cohio "Celio lalo =-34.6 BrCH,...
please answer all of the following questions.
1. [03 pts. For the following reaction, label the nucleophile, electrophile, and leaving group. nucleophile" Lexleasing group 2. [03 pts. Rank the following substrates from most to least reactive in an S2 reaction. 3. [02 pts.) Which of the following is the reaction diagram for endothermic Sn2 reaction? Xo 4. [03 pts.] Draw the major product for the following Sn2 reaction. NaCN 5. [02 pts.) Which reaction in the following pair takes place...
PLEASE ONLY ANSWER FIRST QUESTION
Consider the following reaction: Cd2+ (aq) + 4CN (aq) +- Cd(CN)2- (aq) In this particular reaction CN is acing as a 1. Bronsted Lowry acid 2. Bronsted Lowry base 3. Lewis acid 4. Lewis base 5. Both a and c 6. Both b and d QUESTION 5 The solubility of Zinc hydroxide, Zn(OH)2, in water when dilute nitric acid is added to it? 1. Increases 2. First decreases, then increases 3. Does not change 4....
please i need quick help these questions are due so soon and i
dont know the answers please help me thanks .
Question Completion Status: QUESTION Consider the following acid-base reaction. Equilibrium for this reaction lies to the: OH H-CEC + H-CEC-H + A. right. B. Equilibrium favors neither forward nor reverse reaction. O C. left. D. It cannot be determined. QUESTION 2 Does the equilibrium of this reaction lie to the left or right? BF OH BF3 + A,...
Please answer all 3 questions
QUESTION 32 What is the product from the acid-catalyzed addition of methanol to 22-diethylomirane? CH3OHH 3,3-dimethoxypentane 2-ethyl-1-methoxy-1-butanol 2-ethyl-1-methoxy-2-butanol 2-ethyl-2-methoxy-1-butanol QUESTION 33 What are the products when the following triol is treated with H104? Оно 1 OH OH HIO4 OH 0 0 0 0 w N- QUESTION 34 In which of these Lewis structures would the sulfur be assigned a formal charge of +1? 30 CH-S-0 CH-5-03 CH3-5-C1 CH3-5-CE 2
Question 5 (4 points) What is the major product of the following reaction? 1. NaOET Eto ΟΕΙ 2. Hot O OE EIO OH OE O O- EIO OH OEt OE EtO 애 OEt Question 6 (4 points) Friedel-Crafts acylation reactions cannot be performed on benzoic acid because: The carboxylic acid group gets acylated instead of the aromatic ring. The carboxylic acid group is moderately deactivating preventing any substitution on the aromatic ring. The carboxylic acid group attacks the Lewis acid...
Help on all parts of question 3 would be greatly
appreciated!
3. Treating alkene "A" below with HBr can lead to a number of products. "A" + H-Br A bunch of products. For real, hella products. 3.A. Label the stereocenters in compound "A" as R or S and label the alkene as E or Z. 3.B. Draw the curved arrow mechanism leading to the most stabilized carbo- cation intermediate. (don't do any rearrangements, just acid/base with the alkene) H-Br most...
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