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2. (8 pt) Part A. Give conditions that could be used to catalyze the equilibrium reaction...
In each reaction box, place the best reagent and conditions from the list. Answer Bank acetate...
In each reaction box, place the best reagent and conditions from the list. Answer Bank acetate ion acetone CH, MgBr (excess) H,0,H,O, heat acetic acid NaBH acetyl chloride CH, OH, HO* (cat.) H2O LÃAll | (CHỊ),CHMgBr (excess) NaNH, CH, CH,MgBr (excess) HR UN SEC Question 2 of 11 > Analyze both reactions and indicate whether the equilibrium tends to favor the reactants or the products. > - İri. - immi. 0 Select the true statement(s). O Reactions A and B...
8. For the reaction HCN (%) + H2O (1) HO*)+CN) how would adding OH-shift the equilibrium?...
8. For the reaction HCN (%) + H2O (1) HO*)+CN) how would adding OH-shift the equilibrium? 9. For the reaction Fe(OH)3 (8) Fe' + 3 OH how would adding OH" affect the equilibrium? 10. For the reaction Fe(OH)3 () + Fe 3+ + 3 OH how would adding H30affect the equilibrium? 11. Write the reaction for the combustion of propane gas (CsHx). If the reaction occurs in a closed vessel (no addition or removal of reactants or products) how could...
5. (a) Propose a mechanism for the reaction of 2-bromopyridine with sodium amide to give 2-...
5. (a) Propose a mechanism for the reaction of 2-bromopyridine with sodium amide to give 2- aminopyridine (b) When 3-bromopyridine is used in this reaction, stronger reaction conditions are required to give a mixture of 3-aminopyridine and 4-aminopyridine results. Propose a mechanism which explains this curious result 6. Show the formation of the following reduction products, if the reaction proceeds. If not, propose a different reagent to reduce the starting material! NaBH, (b) NaBH4 KOH OH 1.) LAIH 2.) H,00...
The reaction below has an equilibrium constant of Kp=2.26×104 at 298 K. CO(g)+2H2(g)⇌CH3OH(g) Part A Calculate...
The reaction below has an equilibrium constant of
Kp=2.26×104 at 298 K.
CO(g)+2H2(g)⇌CH3OH(g)
Part A Calculate Kp for the reaction below. CH3OH(g) CO(g)+2H2(g) Submit My Answers Give Up Part B Reactants will be favored at equilibrium. O Products will be favored at equilibrium. Submit My Answers Give Up Part C Calculate Kp for the reaction below. 를 CO (g) + H2 (g)- CH, OH (g) K=
7. MECHANISM: Give the complete stepwise mechanism to account for the following observation. Use curved arrows...
7. MECHANISM: Give the complete stepwise mechanism to account for the following observation. Use curved arrows to show FLOW OF ELECTRONS. [9 points H-CI 8.RETROSYNTHETIC ANALYSIS Give a reasonable synthesis for the following compound from the indicated starting materials. You may use any other organic reagents or inorganic reagents you wish. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate), and products of each synthetic step but NO MECHANISMS. [6 points] OH...
5. (6 pt) Will the product/products be different in this reaction? If yes, show the mechanism. CI et water + Nal rchて (8 pt) Predict the major products in each reaction. Say which mechanism pred...
5. (6 pt) Will the product/products be different in this reaction? If yes, show the mechanism. CI et water + Nal rchて (8 pt) Predict the major products in each reaction. Say which mechanism predominates in case. DO NOT show the mechanisms 6. n2
5. (6 pt) Will the product/products be different in this reaction? If yes, show the mechanism. CI et water + Nal rchて (8 pt) Predict the major products in each reaction. Say which mechanism predominates in...
6. Give the major organic product from each mixed aldol reaction. Then explain why there conditions...
6. Give the major organic product from each mixed aldol reaction. Then explain why there conditions favor one product instead of generating a mixture of products. NaOH HO H CCI, NaOH HO a. LDA ht 7. Give the curved arrow mechanism for this reaction. he NaOH, H2O heat halla Τ Η 3. Give the major organic aldol product for each reaction, along with the dehydration product possible) formed after heating. NaOH heat H2O heat NaOH H2O ix heat NaOH HO
2. Predict the product(s) of each of the reaction conditions below. Specify the substrate type (primary,...
2. Predict the product(s) of each of the reaction conditions
below. Specify the substrate type (primary, secondary, or tertiary
alkyl halide), nucleophile (strong or poor), and the solvent type
(protic or aptrotic). Specify the type of reaction mechanism (SN1
or SN2), show the curved arrow mechanism and draw the products as
3D structures to illustrate stereochemistry.
Predict the product(s) of each of the reaction conditions below. Specify the substrate type (1º, 2º, or 3 alkyl halide). mucleophile (strong or poor),...
6. (1 pt) Which represents an ENDOTHERMIC reaction? a. 10 kJ + reactants - products b....
6. (1 pt) Which represents an ENDOTHERMIC reaction? a. 10 kJ + reactants - products b. reactants-> products + 10 kJ C reactants - products d. reactants-products 7. (1 pt) Which represents a reaction that requires a catalyst? a. 10 kJ + reactants-> products b. reactants -> products + 10 kJ c. reactants products d. reactants-> products 8. (1 pt) Which represents reversible reaction? a. 10 kJ + reactants -> products b. reactants-> products + 10 kJ C. reactants products...
If you could help me with each question and give me a brief explantion, its all...
If you could help me with each question and give me a brief
explantion, its all that I have left to do on my homework, thanks
so much :)
7) Give a complete plausible mechanism for the radical chlorination of the compound to give the product shown: (Show the initiation, propagation, and termination steps.) Cl ses fr e racti sho1) Give the reagents needed to accomplish the following reactions ·w rite you answers on the paper provided for each question!...
In each reaction box, place the best reagent and conditions from the list. Answer Bank acetate ion acetone CH, MgBr (excess) H,0,H,O, heat acetic acid NaBH acetyl chloride CH, OH, HO* (cat.) H2O LÃAll | (CHỊ),CHMgBr (excess) NaNH, CH, CH,MgBr (excess) HR UN SEC Question 2 of 11 > Analyze both reactions and indicate whether the equilibrium tends to favor the reactants or the products. > - İri. - immi. 0 Select the true statement(s). O Reactions A and B...
8. For the reaction HCN (%) + H2O (1) HO*)+CN) how would adding OH-shift the equilibrium? 9. For the reaction Fe(OH)3 (8) Fe' + 3 OH how would adding OH" affect the equilibrium? 10. For the reaction Fe(OH)3 () + Fe 3+ + 3 OH how would adding H30affect the equilibrium? 11. Write the reaction for the combustion of propane gas (CsHx). If the reaction occurs in a closed vessel (no addition or removal of reactants or products) how could...
5. (a) Propose a mechanism for the reaction of 2-bromopyridine with sodium amide to give 2- aminopyridine (b) When 3-bromopyridine is used in this reaction, stronger reaction conditions are required to give a mixture of 3-aminopyridine and 4-aminopyridine results. Propose a mechanism which explains this curious result 6. Show the formation of the following reduction products, if the reaction proceeds. If not, propose a different reagent to reduce the starting material! NaBH, (b) NaBH4 KOH OH 1.) LAIH 2.) H,00...
The reaction below has an equilibrium constant of
Kp=2.26×104 at 298 K.
CO(g)+2H2(g)⇌CH3OH(g)
Part A Calculate Kp for the reaction below. CH3OH(g) CO(g)+2H2(g) Submit My Answers Give Up Part B Reactants will be favored at equilibrium. O Products will be favored at equilibrium. Submit My Answers Give Up Part C Calculate Kp for the reaction below. 를 CO (g) + H2 (g)- CH, OH (g) K=
7. MECHANISM: Give the complete stepwise mechanism to account for the following observation. Use curved arrows to show FLOW OF ELECTRONS. [9 points H-CI 8.RETROSYNTHETIC ANALYSIS Give a reasonable synthesis for the following compound from the indicated starting materials. You may use any other organic reagents or inorganic reagents you wish. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate), and products of each synthetic step but NO MECHANISMS. [6 points] OH...
5. (6 pt) Will the product/products be different in this reaction? If yes, show the mechanism. CI et water + Nal rchて (8 pt) Predict the major products in each reaction. Say which mechanism predominates in case. DO NOT show the mechanisms 6. n2
5. (6 pt) Will the product/products be different in this reaction? If yes, show the mechanism. CI et water + Nal rchて (8 pt) Predict the major products in each reaction. Say which mechanism predominates in...
6. Give the major organic product from each mixed aldol reaction. Then explain why there conditions favor one product instead of generating a mixture of products. NaOH HO H CCI, NaOH HO a. LDA ht 7. Give the curved arrow mechanism for this reaction. he NaOH, H2O heat halla Τ Η 3. Give the major organic aldol product for each reaction, along with the dehydration product possible) formed after heating. NaOH heat H2O heat NaOH H2O ix heat NaOH HO
2. Predict the product(s) of each of the reaction conditions
below. Specify the substrate type (primary, secondary, or tertiary
alkyl halide), nucleophile (strong or poor), and the solvent type
(protic or aptrotic). Specify the type of reaction mechanism (SN1
or SN2), show the curved arrow mechanism and draw the products as
3D structures to illustrate stereochemistry.
Predict the product(s) of each of the reaction conditions below. Specify the substrate type (1º, 2º, or 3 alkyl halide). mucleophile (strong or poor),...
6. (1 pt) Which represents an ENDOTHERMIC reaction? a. 10 kJ + reactants - products b. reactants-> products + 10 kJ C reactants - products d. reactants-products 7. (1 pt) Which represents a reaction that requires a catalyst? a. 10 kJ + reactants-> products b. reactants -> products + 10 kJ c. reactants products d. reactants-> products 8. (1 pt) Which represents reversible reaction? a. 10 kJ + reactants -> products b. reactants-> products + 10 kJ C. reactants products...
If you could help me with each question and give me a brief
explantion, its all that I have left to do on my homework, thanks
so much :)
7) Give a complete plausible mechanism for the radical chlorination of the compound to give the product shown: (Show the initiation, propagation, and termination steps.) Cl ses fr e racti sho1) Give the reagents needed to accomplish the following reactions ·w rite you answers on the paper provided for each question!...
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