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- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(OpenStax)/31%3A_Synthetic_Polymers/31.04%3A_Step-Growth_PolymersOften, the reactions used to link these monomers include multiple nucleophilic acyl substitutions. Step-growth polymerizations usually use two different monomers, neither of which would undergo polyme...Often, the reactions used to link these monomers include multiple nucleophilic acyl substitutions. Step-growth polymerizations usually use two different monomers, neither of which would undergo polymerization on its own. The two monomers are multifuntional and complementary to each other, such that each provides the other with a reactive partner. In this section, we will be focusing on monomers which are difunctional, meaning they contain two of the same reactive functional group.
- https://chem.libretexts.org/Workbench/LCDS_Organic_Chemistry_OER_Textbook_-_Todd_Trout/31%3A_Synthetic_Polymers/31.05%3A_Step-Growth_PolymersOften, the reactions used to link these monomers include multiple nucleophilic acyl substitutions. Step-growth polymerizations usually use two different monomers, neither of which would undergo polyme...Often, the reactions used to link these monomers include multiple nucleophilic acyl substitutions. Step-growth polymerizations usually use two different monomers, neither of which would undergo polymerization on its own. The two monomers are multifuntional and complementary to each other, such that each provides the other with a reactive partner. In this section, we will be focusing on monomers which are difunctional, meaning they contain two of the same reactive functional group.
- https://chem.libretexts.org/Courses/Williams_School/Chemistry_II/10%3A_Synthetic_Polymers/10.04%3A_Step-Growth_PolymersThe first “6” stands for the number of carbons in the diamine monomer while the second number indicated the number of carbons in the dicarboxylic acid. The carbon dioxide evolved is the foaming agent,...The first “6” stands for the number of carbons in the diamine monomer while the second number indicated the number of carbons in the dicarboxylic acid. The carbon dioxide evolved is the foaming agent, and the amino groups formed at the same time extend the polymer chains by reacting with the residual isocyano end groups to form urea linkages:
- https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/30%3A_Synthetic_Polymers/30.04%3A_Step-Growth_PolymersOften, the reactions used to link these monomers include multiple nucleophilic acyl substitutions. Step-growth polymerizations usually use two different monomers, neither of which would undergo polyme...Often, the reactions used to link these monomers include multiple nucleophilic acyl substitutions. Step-growth polymerizations usually use two different monomers, neither of which would undergo polymerization on its own. The two monomers are multifuntional and complementary to each other, such that each provides the other with a reactive partner. In this section, we will be focusing on monomers which are difunctional, meaning they contain two of the same reactive functional group.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_III_(Morsch_et_al.)/30%3A_Synthetic_Polymers/30.04%3A_Step-Growth_PolymersOften, the reactions used to link these monomers include multiple nucleophilic acyl substitutions. Step-growth polymerizations usually use two different monomers, neither of which would undergo polyme...Often, the reactions used to link these monomers include multiple nucleophilic acyl substitutions. Step-growth polymerizations usually use two different monomers, neither of which would undergo polymerization on its own. The two monomers are multifuntional and complementary to each other, such that each provides the other with a reactive partner. In this section, we will be focusing on monomers which are difunctional, meaning they contain two of the same reactive functional group.
- https://chem.libretexts.org/Workbench/Pick_Your_Poison%3A_Introduction_to_Materials_Toxicology/31%3A_Synthetic_Polymers/31.05%3A_Step-Growth_PolymersOften, the reactions used to link these monomers include multiple nucleophilic acyl substitutions. Step-growth polymerizations usually use two different monomers, neither of which would undergo polyme...Often, the reactions used to link these monomers include multiple nucleophilic acyl substitutions. Step-growth polymerizations usually use two different monomers, neither of which would undergo polymerization on its own. The two monomers are multifuntional and complementary to each other, such that each provides the other with a reactive partner. In this section, we will be focusing on monomers which are difunctional, meaning they contain two of the same reactive functional group.
- https://chem.libretexts.org/Courses/can/CHEM_232_-_Organic_Chemistry_II_(Puenzo)/16%3A_Synthetic_Polymers/16.05%3A_Step-Growth_PolymersOften, the reactions used to link these monomers include multiple nucleophilic acyl substitutions. Step-growth polymerizations usually use two different monomers, neither of which would undergo polyme...Often, the reactions used to link these monomers include multiple nucleophilic acyl substitutions. Step-growth polymerizations usually use two different monomers, neither of which would undergo polymerization on its own. The two monomers are multifuntional and complementary to each other, such that each provides the other with a reactive partner. In this section, we will be focusing on monomers which are difunctional, meaning they contain two of the same reactive functional group.
