Loading [MathJax]/extensions/mml2jax.js
Skip to main content
Library homepage
 

Text Color

Text Size

 

Margin Size

 

Font Type

Enable Dyslexic Font
Chemistry LibreTexts

Search

  • Filter Results
  • Location
  • Classification
    • Article type
    • Stage
    • Author
    • Show Page TOC
    • Cover Page
    • License
    • Transcluded
    • Number of Print Columns
    • PrintOptions
    • OER program or Publisher
    • Student Analytics
    • Autonumber Section Headings
    • License Version
    • Print CSS
  • Include attachments
Searching in
About 16 results
  • https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(OpenStax)/31%3A_Synthetic_Polymers/31.04%3A_Step-Growth_Polymers
    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 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_Polymers
    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 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_Polymers
    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 ...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_Polymers
    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 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_reactions
    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 ...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_Polymers
    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 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_Polymers
    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 ...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_Polymers
    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 ...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_Polymers
    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 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_Polymers
    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 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_Polymers
    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 ...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 .

Support Center

How can we help?