another organic chemistry question....please help! mechanisms and reaction problems
Homework Answers
I have taken the same set of reactant in two solvents
In water, the alkyl halide and KI both are soluble so they can react back to give the reactants again as the reaction is in equilibrium.
So to shift the equilibrium towards right or product side, there is a need to remove atleast one of the product. This is achieved by removing KCl by taking acetone as solvent. In acetone, KCl is insoluble hence will precipitate out.
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another organic chemistry question....please help! mechanisms and
reaction problems
Organic chemistry 2 question I need help with problems #1 and #2, please showed works and...
Organic chemistry 2 question
I need help with problems #1 and #2, please showed works and neat
writing, thank you
Please help answer the following organic chemistry problems, thank you!
Please help answer the following organic chemistry problems, thank
you!
Organic Chemistry. Need help with this mechanisms. Please show all arrows and charges. Thank you Provide...
Organic Chemistry. Need help with this
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Provide the mechanism for the transformation shown below. You must use arrows indicating movement of electrons in order to receive full credit.
Chemistry Organic Chemistry Problems Elimination Reactions Problem 5: Which of the product in the following reaction...
Chemistry Organic Chemistry Problems Elimination Reactions Problem 5: Which of the product in the following reaction will form and why. Use mechanism and relevant drawings to explain your answer. Br Problem 6: What is the product of the following reaction? sodium methoxide methanol sodium methoxide methanol Organic Chemistry Organic Chemistry Problems Elimination Reactions Problem 10: Use mechanism to explain all of the products for the reaction below. OH H2SO4 heat
Hi, Can someone help me with the following organic chemistry question regarding mechanisms? Thank you so...
Hi,
Can someone help me with the following organic chemistry
question regarding mechanisms?
Thank you so much! I will give a thumbs up if it's answered
well!
Explain the product ratios obtained below. Your explanation should include the mechanism(s) for the rate-limiting step(s) of each reaction, and an approx. 100-word discussion. hv 86% 14% 1 - 2x Br2 hv <1% >99%
please help with organic chemistry! mechanisms? 5) The reaction of 2-bromo-1,1-dimethylcyclohexane with methanol gives the following...
please help with organic chemistry! mechanisms?
5) The reaction of 2-bromo-1,1-dimethylcyclohexane with methanol gives the following products. Please provide a detailed explanation to the formation of each product. You should use structures of intermediates in your answer. (8 points). осн, CH,он OCH Br + 6) There are a variety of isomeric 1,2,3,4,5,6-hexachlorocyclohexanes, but one of them does not react with CH3CH20' to give an elimination product. Provide the structure of this compound and briefly explain why it does not react...
Need help with this organic chemistry problem please. Need help with this organic chemistry problem please....
Need help with this organic chemistry problem please.
Need help with this organic chemistry problem please. What s the driving force that leads to the observed product rather than the molecule below?
Please help organic chemistry provide a reasonable reaction mechanism for the following reaction Answer both parts...
Please help organic chemistry
provide a reasonable reaction mechanism for the following reaction Answer both parts of the following question. Provide a synthesis of the following substance from the indicated starting materials. You may assume that you have any needed inorganic regents provide a mechanism for each step of the following process.
*Organic chemistry please help* In each reaction box, place the best reagent and conditions from the...
*Organic chemistry please help* In each reaction box, place the
best reagent and conditions from the list below.
The following question is based on Organic Chemistry Lab. The experiment is Diels Alder reaction. Please...
The following question is based on Organic Chemistry Lab. The
experiment is Diels Alder reaction. Please answer question number 2
and 3.
Organic chemistry 2 question
I need help with problems #1 and #2, please showed works and neat
writing, thank you
Please help answer the following organic chemistry problems, thank
you!
Organic Chemistry. Need help with this
mechanisms. Please show all arrows and charges. Thank you
Provide the mechanism for the transformation shown below. You must use arrows indicating movement of electrons in order to receive full credit.
Chemistry Organic Chemistry Problems Elimination Reactions Problem 5: Which of the product in the following reaction will form and why. Use mechanism and relevant drawings to explain your answer. Br Problem 6: What is the product of the following reaction? sodium methoxide methanol sodium methoxide methanol Organic Chemistry Organic Chemistry Problems Elimination Reactions Problem 10: Use mechanism to explain all of the products for the reaction below. OH H2SO4 heat
Hi,
Can someone help me with the following organic chemistry
question regarding mechanisms?
Thank you so much! I will give a thumbs up if it's answered
well!
Explain the product ratios obtained below. Your explanation should include the mechanism(s) for the rate-limiting step(s) of each reaction, and an approx. 100-word discussion. hv 86% 14% 1 - 2x Br2 hv <1% >99%
please help with organic chemistry! mechanisms?
5) The reaction of 2-bromo-1,1-dimethylcyclohexane with methanol gives the following products. Please provide a detailed explanation to the formation of each product. You should use structures of intermediates in your answer. (8 points). осн, CH,он OCH Br + 6) There are a variety of isomeric 1,2,3,4,5,6-hexachlorocyclohexanes, but one of them does not react with CH3CH20' to give an elimination product. Provide the structure of this compound and briefly explain why it does not react...
Need help with this organic chemistry problem please.
Need help with this organic chemistry problem please. What s the driving force that leads to the observed product rather than the molecule below?
Please help organic chemistry
provide a reasonable reaction mechanism for the following reaction Answer both parts of the following question. Provide a synthesis of the following substance from the indicated starting materials. You may assume that you have any needed inorganic regents provide a mechanism for each step of the following process.
*Organic chemistry please help* In each reaction box, place the
best reagent and conditions from the list below.
The following question is based on Organic Chemistry Lab. The
experiment is Diels Alder reaction. Please answer question number 2
and 3.
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