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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/can/CHEM_232_-_Organic_Chemistry_II_(Puenzo)/07%3A_Carboxylic_Acid_Derivatives-_Nucleophilic_Acyl_Substitution_Reactions/7.10%3A_Polyamides_and_Polyesters_-_Step-Growth_Polymersu s e d i n e n g i n e e r i n g a r e s t r o n g , t o u g h m a t e r i a l s , a n d s o m e g r a d e s a r e o p t i c a l l y t r a n s p a r e n t . T h e y a r e e a s i l y w o r k e d , m ...u s e d i n e n g i n e e r i n g a r e s t r o n g , t o u g h m a t e r i a l s , a n d s o m e g r a d e s a r e o p t i c a l l y t r a n s p a r e n t . T h e y a r e e a s i l y w o r k e d , m o l d e d , a n d t h e r m o f o r m e d . B e c a u s e o f t h e s e p r o p e r t i e s , p o l y c a r b o n a t e s 1) P r o v i d e s t r u c t u r e s o f t h e p o l y e s t e r s m a d e f r o m t h e m o n o m e r s a s i n d i c a t e d .
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(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/Bookshelves/Introductory_Chemistry/Introduction_to_Organic_and_Biochemistry_(Malik)/04%3A_Organic_reactions/4.05%3A_Nucleophilic_acyl_substitution_reactionsNucleophilic acyl substitution reaction mechanisms and their applications to the reactions of carboxylic acid and their derivatives are described. Applications of these reactions for the synthesis of ...Nucleophilic acyl substitution reaction mechanisms and their applications to the reactions of carboxylic acid and their derivatives are described. Applications of these reactions for the synthesis of condensation polymers are also described.
- 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/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/21%3A_Carboxylic_Acid_Derivatives-_Nucleophilic_Acyl_Substitution_Reactions/21.10%3A_Polyamides_and_Polyesters-_Step-Growth_Polymersu s e d i n e n g i n e e r i n g a r e s t r o n g , t o u g h m a t e r i a l s , a n d s o m e g r a d e s a r e o p t i c a l l y t r a n s p a r e n t . T h e y a r e e a s i l y w o r k e d , m ...u s e d i n e n g i n e e r i n g a r e s t r o n g , t o u g h m a t e r i a l s , a n d s o m e g r a d e s a r e o p t i c a l l y t r a n s p a r e n t . T h e y a r e e a s i l y w o r k e d , m o l d e d , a n d t h e r m o f o r m e d . B e c a u s e o f t h e s e p r o p e r t i e s , p o l y c a r b o n a t e s 1) P r o v i d e s t r u c t u r e s o f t h e p o l y e s t e r s m a d e f r o m t h e m o n o m e r s a s i n d i c a t e d .
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_II_(Morsch_et_al.)/21%3A_Carboxylic_Acid_Derivatives-_Nucleophilic_Acyl_Substitution_Reactions/21.09%3A_Polyamides_and_Polyesters_-_Step-Growth_Polymersu s e d i n e n g i n e e r i n g a r e s t r o n g , t o u g h m a t e r i a l s , a n d s o m e g r a d e s a r e o p t i c a l l y t r a n s p a r e n t . T h e y a r e e a s i l y w o r k e d , m ...u s e d i n e n g i n e e r i n g a r e s t r o n g , t o u g h m a t e r i a l s , a n d s o m e g r a d e s a r e o p t i c a l l y t r a n s p a r e n t . T h e y a r e e a s i l y w o r k e d , m o l d e d , a n d t h e r m o f o r m e d . B e c a u s e o f t h e s e p r o p e r t i e s , p o l y c a r b o n a t e s 1) P r o v i d e s t r u c t u r e s o f t h e p o l y e s t e r s m a d e f r o m t h e m o n o m e r s a s i n d i c a t e d .
- 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/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/21%3A_Carboxylic_Acid_Derivatives-_Nucleophilic_Acyl_Substitution_Reactions/21.09%3A_Polyamides_and_Polyesters_-_Step-Growth_Polymersu s e d i n e n g i n e e r i n g a r e s t r o n g , t o u g h m a t e r i a l s , a n d s o m e g r a d e s a r e o p t i c a l l y t r a n s p a r e n t . T h e y a r e e a s i l y w o r k e d , m ...u s e d i n e n g i n e e r i n g a r e s t r o n g , t o u g h m a t e r i a l s , a n d s o m e g r a d e s a r e o p t i c a l l y t r a n s p a r e n t . T h e y a r e e a s i l y w o r k e d , m o l d e d , a n d t h e r m o f o r m e d . B e c a u s e o f t h e s e p r o p e r t i e s , p o l y c a r b o n a t e s 1) P r o v i d e s t r u c t u r e s o f t h e p o l y e s t e r s m a d e f r o m t h e m o n o m e r s a s i n d i c a t e d .