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![E ots moon with Naon the substitution occur via SN2 mechanism. Mechanism 9 In NG οτς Naon an [SN2] ots 5-Coordinated transiti](http://img.homeworklib.com/questions/2da40d20-d2dc-11eb-a101-2d92ef3448b1.png?x-oss-process=image/resize,w_560)
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Which reagent is necessary for this transformation? for Joomom o sodium ethoxide potassium...
Which reagent is necessary for this transformation? on Jason a sodium ethoxide O potassium hydroxide O...
Which reagent is necessary for this transformation? on Jason a sodium ethoxide O potassium hydroxide O ethanol ethyl bromide Question 11 4 pts Predict the starting material for this reaction. Hys D -SH (1S,3S)-3-methylcyclopentane-1-thiol (15,3S)-1-iodo-3-methylcyclopentane (1R 3R)-1-iodo-3-methylcyclopentane (10,3S)-1-lodo-3-methylcyclopentane (15. 3 Lclodomethylaconentane
Question 11 4 pts Predict the starting material for this reaction. HS (18,3S)-3-methylcyclopentane-1-thiol (15,35-1-iodo-3-methylcyclopentane (1R 3R)-1-iodo-3-methylcyclopentane...
Question 11 4 pts Predict the starting material for this reaction. HS (18,3S)-3-methylcyclopentane-1-thiol (15,35-1-iodo-3-methylcyclopentane (1R 3R)-1-iodo-3-methylcyclopentane (1R 3S)-1-iodo-3-methylcyclopentane (15,3R)-1-iodo-3-methylcyclopentane
D Question 10 4 pts Which reagent is necessary for this transformation? Moro - Joensen o...
D Question 10 4 pts Which reagent is necessary for this transformation? Moro - Joensen o sodium ethoxide potassium hydroxide ethanol ethyl bromide
Malonic ester (diethyl malonate) is treated successively with sodium ethoxide (1 eq.), ethyl bromide, potassium tert-butoxide,...
Malonic ester (diethyl malonate) is treated successively with sodium ethoxide (1 eq.), ethyl bromide, potassium tert-butoxide, isobutyl chloride, hot aqueous NaOH HCI, and heat. What is the final product? 6-Methylheptanoic acid • 2-Ethyl-3-methylpentanoic acid HE Ethylisobutylmalonic acid 4-Ethyl-2-methylpentanoic acid 2 Ethyl-4-methylpentanoic acid
The tosylate of (2R, 3R)-3-phenylbutan-2-ol undergoes an E2 elimination on treatment with sodium ethoxide. Draw the...
The tosylate of (2R, 3R)-3-phenylbutan-2-ol undergoes an E2 elimination on treatment with sodium ethoxide. Draw the structure of the alkene that is produced. Use the wedge hash bond tools to indicate stereochemistry. You do not have to explicitly draw H atoms. If a group is achiral, do not me wedged or hashed bonds on it. Predict the major alkene product of the following E1 reaction: Amines are converted into alkene5, by a two-step process called the Hofmann elimination. S_N 2...
select the reagent that will accomplish the given transformation Question 12: A B 1. Cly, hv....
select the reagent that will accomplish the given
transformation
Question 12: A B 1. Cly, hv. CCL 2. H20 | 3. Cros. H20. H2SO. 1. Cl. hv. CCL 2 NaOH, HO 3. Cros. H2O, H,SO 1. Brą, hv. CBA 2. HO 3. CrO2, H20, H2SO4 1. Cly, hv. CCI 2. NaOH, HO 3. PCC, DCM For the following section, questions 13-20, answer the given questions Question 13: What would be the major product of the reaction below? A. (1R 2R)-1-ethoxy-2-methylcyclohexane...
please help with these ASAP, thanks! What is the best reagent(s) for the following transformation? OH...
please help with these ASAP, thanks!
What is the best reagent(s) for the following transformation? OH O NaOH, heat CH3CH2OH, H2S04 OmCPBA O 1. LiAlH4 2. H30+ What is the major product in the following reaction? 1. DIBAL 2. H20 H OH o" ОН What is the major product in the following reaction? LIAIHA 2 H20 "NH2 NH2
How would I go about solving question 1 in the image? How would I draw the...
How would I go about solving question 1 in the image?
How would I draw the major products?
I. (24 pts.) Indicate the type of reaction that will predominate (i.e., S1, SN2, E1, or E2), and when draw the structure of the major product when: 1. isopropyl chloride reacts with hydroxide predominate rxn. structure: 3. 2-iodopentane reacts with ethoxide in DMSO predominate rxn. structure: 2. t-butyl tosylate reacts with CH3OH predominate rxn. structure: 4. ethyl bromide reacts with CH30- predominate...
PLEASE HELP FAST!!! 1. Predict the major product of the reaction. Clearly indicate stereochemistry, if necessary...
PLEASE HELP FAST!!!
1. Predict the major product of the reaction. Clearly indicate stereochemistry, if necessary (3 pts) H 1.9-BBN-H THE Me Me 2. NaOH H202 2. Provide reagents to achieve the shown multi-step transformations. (6 pts) H Me Me Br Br Me Br Br 3. Draw a detailed arrow-pushing mechanism for the following transformation. (4 pts) Ph Li(0) Ph Ph Ph NH30)
Please help with both. U Question 15 3 What is the major product formed upon radical...
Please help with both.
U Question 15 3 What is the major product formed upon radical bromination of (S) 3-methyhexane? O (R) 3-bromo-3-methylhexane (S) 3-bromo-3-methylhexane O (3R) 1-bromo-3-methylhexane o a mixture of (R) and (S) 3-bromo-3-methylhexane U Question 16 3 pts What is the major organic product obtained from the following reaction? CHECO,H Hw HW WH HyC2 CHE Hzc 3 H O only 3 O both 2 and 3 O only 1 O only 2
Which reagent is necessary for this transformation? on Jason a sodium ethoxide O potassium hydroxide O ethanol ethyl bromide Question 11 4 pts Predict the starting material for this reaction. Hys D -SH (1S,3S)-3-methylcyclopentane-1-thiol (15,3S)-1-iodo-3-methylcyclopentane (1R 3R)-1-iodo-3-methylcyclopentane (10,3S)-1-lodo-3-methylcyclopentane (15. 3 Lclodomethylaconentane
Question 11 4 pts Predict the starting material for this reaction. HS (18,3S)-3-methylcyclopentane-1-thiol (15,35-1-iodo-3-methylcyclopentane (1R 3R)-1-iodo-3-methylcyclopentane (1R 3S)-1-iodo-3-methylcyclopentane (15,3R)-1-iodo-3-methylcyclopentane
D Question 10 4 pts Which reagent is necessary for this transformation? Moro - Joensen o sodium ethoxide potassium hydroxide ethanol ethyl bromide
Malonic ester (diethyl malonate) is treated successively with sodium ethoxide (1 eq.), ethyl bromide, potassium tert-butoxide, isobutyl chloride, hot aqueous NaOH HCI, and heat. What is the final product? 6-Methylheptanoic acid • 2-Ethyl-3-methylpentanoic acid HE Ethylisobutylmalonic acid 4-Ethyl-2-methylpentanoic acid 2 Ethyl-4-methylpentanoic acid
The tosylate of (2R, 3R)-3-phenylbutan-2-ol undergoes an E2 elimination on treatment with sodium ethoxide. Draw the structure of the alkene that is produced. Use the wedge hash bond tools to indicate stereochemistry. You do not have to explicitly draw H atoms. If a group is achiral, do not me wedged or hashed bonds on it. Predict the major alkene product of the following E1 reaction: Amines are converted into alkene5, by a two-step process called the Hofmann elimination. S_N 2...
select the reagent that will accomplish the given
transformation
Question 12: A B 1. Cly, hv. CCL 2. H20 | 3. Cros. H20. H2SO. 1. Cl. hv. CCL 2 NaOH, HO 3. Cros. H2O, H,SO 1. Brą, hv. CBA 2. HO 3. CrO2, H20, H2SO4 1. Cly, hv. CCI 2. NaOH, HO 3. PCC, DCM For the following section, questions 13-20, answer the given questions Question 13: What would be the major product of the reaction below? A. (1R 2R)-1-ethoxy-2-methylcyclohexane...
please help with these ASAP, thanks!
What is the best reagent(s) for the following transformation? OH O NaOH, heat CH3CH2OH, H2S04 OmCPBA O 1. LiAlH4 2. H30+ What is the major product in the following reaction? 1. DIBAL 2. H20 H OH o" ОН What is the major product in the following reaction? LIAIHA 2 H20 "NH2 NH2
How would I go about solving question 1 in the image?
How would I draw the major products?
I. (24 pts.) Indicate the type of reaction that will predominate (i.e., S1, SN2, E1, or E2), and when draw the structure of the major product when: 1. isopropyl chloride reacts with hydroxide predominate rxn. structure: 3. 2-iodopentane reacts with ethoxide in DMSO predominate rxn. structure: 2. t-butyl tosylate reacts with CH3OH predominate rxn. structure: 4. ethyl bromide reacts with CH30- predominate...
PLEASE HELP FAST!!!
1. Predict the major product of the reaction. Clearly indicate stereochemistry, if necessary (3 pts) H 1.9-BBN-H THE Me Me 2. NaOH H202 2. Provide reagents to achieve the shown multi-step transformations. (6 pts) H Me Me Br Br Me Br Br 3. Draw a detailed arrow-pushing mechanism for the following transformation. (4 pts) Ph Li(0) Ph Ph Ph NH30)
Please help with both.
U Question 15 3 What is the major product formed upon radical bromination of (S) 3-methyhexane? O (R) 3-bromo-3-methylhexane (S) 3-bromo-3-methylhexane O (3R) 1-bromo-3-methylhexane o a mixture of (R) and (S) 3-bromo-3-methylhexane U Question 16 3 pts What is the major organic product obtained from the following reaction? CHECO,H Hw HW WH HyC2 CHE Hzc 3 H O only 3 O both 2 and 3 O only 1 O only 2
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