please explain the polycondensation reaction of 1,6 diaminohexane and adipoyl chloride creating nylon 6,6 why would...
Homework Answers
Overall reaction is an example e nucleophilic addition and water is formed as biproduct.
Amide is the functional group in the product and it is water sensitive and undergo hydrolysis to get back starting material
Hence it is water sensitive reaction.
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please explain the polycondensation reaction of 1,6 diaminohexane
and adipoyl chloride creating nylon 6,6
why would...
Can you answer these questions based on the Synthesis of Nylon-6,6 using adipoyl chloride and 1,6-hexanediamine...
Can you answer these questions based on the Synthesis of Nylon-6,6 using adipoyl chloride and 1,6-hexanediamine Discuss the polycondensation reaction. Why would water interfere with it? In case experiment failed-explanation is expected. Why it failed? What could be improved. Explain molecular structure vs signal relationship . In your discussion consider the following concepts: polycondensation, functional groups, fibril formation and stabilization (interchain molecular itneractions) , reaction yield and the role of NaOH solution used in the reaction
Backkground on condensation polymers and what happens (in details) when 1,6-diaminohexane and adipoyl chloride mix.
Backkground on condensation polymers and what happens (in details) when 1,6-diaminohexane and adipoyl chloride mix.
What is the purpose of adipoyl chloride, 5% aqeous solution of 1,6 hexane diamine, cyclohexane and...
What is the purpose of adipoyl chloride, 5% aqeous solution of 1,6 hexane diamine, cyclohexane and NaOH in synthesis of Nylon-6,6?
Discuss the polycondensation reaction. Why would water interfere with it? In case experiment failed-explanation is expected....
Discuss the polycondensation reaction. Why would water interfere with it? In case experiment failed-explanation is expected. Why it failed? What could be improved. Explain molecular structure vs signal relationship . In your discussion consider the following concepts: polycondensation, functional groups, fibril formation and stabilization (interchain molecular itneractions) , reaction yield and the role of NaOH solution used in the reaction Can you answer these questions based on the Synthesis of Nylon-6,6 using adipoyl chloride and 1,6-hexanediamine
This is for a polymer lab. Please answer all parts of the questions clearly and explain...
This is for a polymer lab. Please answer all parts of the
questions clearly and explain thoroughly. Thank You!
1. In the process of nylon preparation, NaOH was added to the reaction mixture even though it does not appear in the equation for the preparation of nylon. What function does the NaOH have in the process? (Hint: Consider all the products of the nylon reaction.) 2. How many 1,6-diaminohexane monomers and adipoyl chloride monomers are required to make a nylon...
* Densities of the two reactants are: Sebacoyl chloride 1.121 g/mL and, 1,6-diaminohexane 0.83 g/mL yion Co1o o-diaminohexane Se ba coyl chloride If I start with 2 mL of the sebacoyl chloride and 1.3...
* Densities of the two reactants are: Sebacoyl chloride 1.121
g/mL and, 1,6-diaminohexane 0.83 g/mL
yion Co1o o-diaminohexane Se ba coyl chloride If I start with 2 mL of the sebacoyl chloride and 1.3 mL 1,6- diaminohexane and end up with 3.30g of my product nylon 6,10 what is my percent yield?
yion Co1o o-diaminohexane Se ba coyl chloride If I start with 2 mL of the sebacoyl chloride and 1.3 mL 1,6- diaminohexane and end up with 3.30g of...
10 mL of 0.59M 1,6-diaminohexane and 10 mL of 0.29M Sebacoyl chloride are used to make nylon 6.10. The final product weight was 1.36g. Calculate the percent yield? Use the MW of one repeating monomer...
10 mL of 0.59M 1,6-diaminohexane and 10 mL of 0.29M Sebacoyl chloride are used to make nylon 6.10. The final product weight was 1.36g. Calculate the percent yield? Use the MW of one repeating monomer for the weight of the product? Please show all work.
Please provide a detailed mechanism of initial steps of polymerization reaction between adipoyl chlorideand 1,6-hexanediamine (up...
Please provide a detailed mechanism of initial steps of polymerization reaction between adipoyl chlorideand 1,6-hexanediamine (up to trimer formation). Please include arrows, electron flow and lone pairs.
In reference to: (Polymerization; Nylon-6,6 Organic Chemistry Lab) 1. Why do you add hydroxide to your...
In reference to: (Polymerization; Nylon-6,6 Organic Chemistry Lab) 1. Why do you add hydroxide to your hexanediamine solution? What would occur if you did not add it?
PLEASE DO NOT WRITE BY HAND!! Please answer these three questions. 1. Why would the rate...
PLEASE DO NOT WRITE BY HAND!!
Please answer these three questions.
1. Why would the rate of reaction be slower if the following
ester was used in place of adipoyl chloride?
2. The product of the following reaction is commonly known is
Kevlar. Draw the polymer product of the following reaction.
3. Acid chlorides react with a wide variety of nucleophiles.
What is the product of the following reaction where a diol is used
as a nucleophile?
This is for a polymer lab. Please answer all parts of the
questions clearly and explain thoroughly. Thank You!
1. In the process of nylon preparation, NaOH was added to the reaction mixture even though it does not appear in the equation for the preparation of nylon. What function does the NaOH have in the process? (Hint: Consider all the products of the nylon reaction.) 2. How many 1,6-diaminohexane monomers and adipoyl chloride monomers are required to make a nylon...
* Densities of the two reactants are: Sebacoyl chloride 1.121
g/mL and, 1,6-diaminohexane 0.83 g/mL
yion Co1o o-diaminohexane Se ba coyl chloride If I start with 2 mL of the sebacoyl chloride and 1.3 mL 1,6- diaminohexane and end up with 3.30g of my product nylon 6,10 what is my percent yield?
yion Co1o o-diaminohexane Se ba coyl chloride If I start with 2 mL of the sebacoyl chloride and 1.3 mL 1,6- diaminohexane and end up with 3.30g of...
PLEASE DO NOT WRITE BY HAND!!
Please answer these three questions.
1. Why would the rate of reaction be slower if the following
ester was used in place of adipoyl chloride?
2. The product of the following reaction is commonly known is
Kevlar. Draw the polymer product of the following reaction.
3. Acid chlorides react with a wide variety of nucleophiles.
What is the product of the following reaction where a diol is used
as a nucleophile?
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