Provide the starting materials for:
1. Nylon 46 [poly(tetramethylene adipamide)] (and what is the structure of adipic acid?)
2. Poly(1,4-cyclohexylenedimethylene suberamide)
Provide the starting materials for: 1. Nylon 46 [poly(tetramethylene adipamide)] (and what is the structure of...
Hexamethylenediamine (C6H16N2) is one of the starting materials for the production of nylon. It can be prepared from adipic acid (C6H1004) by the following overall equation: C&H100 (1) + 2NH2() + 4H2(g) + CH16N (1) + 4H2O(1) What is the percent yield for the reaction if 1.72 x 109 g of hexamethylenediamine is made from 2.56 x 100 g of adipic acid? Percent yield Submit Answer Retry Entire Group 9 more group attempts remaining
1) Nylon [6.10] can also be prepared starting with the diacid sebacic acid, a shelf-stable white solid with no hazardous vapors. Propose a synthesis of Nylon starting with sebacic acid. 2) The strength of nylon fibers comes from the hydrogen bonding between polymer strands. Draw two nylon [6.10] strands and illustrate the hydrogen bonding between them. Show the work
1) Nylon [6.10] can also be prepared starting with the diacid sebacic acid, a shelf-stable white solid with no hazardous vapors. Propose a synthesis of Nylon starting with sebacic acid. 2) The strength of nylon fibers comes from the hydrogen bonding between polymer strands. Draw two nylon [6.10] strands and illustrate the hydrogen bonding between them. Show the work
This is a dry lab assessment for synthesis of Nylon 6,6. I believe I understand how to calculate the limiting reagent (Q1) and have determined it to be adipic acid. I’m stuck on calculating the theoretical yield (Q2) and need some help getting through the bullet points of the procedure used to answer the question. Thanks! 1. In the experiment, you are instructed to use 0.500 g of adipic acid and 0.40 g of hexamethylenediamine. Calculate the mmol of each...
provide the structure of the monomer that would produce Nylon 66....please draw out the structure so I can see it ) *+--NH(CHz)6NHC(CH2)4C-+* Nylon 66 0 o *n olic OllC d
Starting materials used; - 1mL sebacoyl chloride - 50 mL hexane - 2.5 mL 1,6-diaminohexane - 25 mL 3% sodium hydroxide Final products; - 0.94 g adipic acid - 1,6-hexamethylenediamine Calculate the theoretical yield adipic acid if the actual yield is 0.94g?
1. Provide the missing starting materials, reagents, or products in each of the following reactions. H+ OH CH,OH NaOH Meo NH2 room temp. HO OH Meo Me ОН Meo 2. Provide appropriate conditions to convert each of the following starting mana hexanoic acid (some transformations may require more than one step): It each of the following starting materials into OH OH ОMe "NH₂
Provide mechanisms (with arrows) for the formation of Nylon-6,10 and polystyrene from their constituted monomers. What is the role of the aqueous base in the nylon synthesis? What is the role of sulfuric acid in the polystyrene synthesis?
Provide mechanisms (with arrows) for the formation of Nylon-6,10 from hexamethlenediamine and sebacoyl chloride , and polystyrene from 1,2-dichloroethane and sulfuric acid. What is the role of the aqueous base in the nylon synthesis? What is the role of sulfuric acid in the polystyrene synthesis?
please provide the structure and IUPAC name for each 7. Acetic acid Systematic name=ethanoic acid colorless liquid organic compound w chem Structure and IUPAC name for: o formula CH3COOH • Oxalic acid (oh) HOC- Cloh • Malonic acid (my) • Succinic acid (such) • Glutaric acid (good) • Adipic acid (apple) • Pimelic acid (pie)