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- https://chem.libretexts.org/Courses/can/CHEM_232_-_Organic_Chemistry_II_(Puenzo)/16%3A_Synthetic_Polymers/16.02%3A_Chain-Growth_PolymersPolymers resulting from additions to alkenes monomers are chain-growth polymers. In these processes each addition step results in a longer chain which ends in a reactive site. The mechanism of each ad...Polymers resulting from additions to alkenes monomers are chain-growth polymers. In these processes each addition step results in a longer chain which ends in a reactive site. The mechanism of each addition step is the same, and each addition step adds another monomer to extend the chain by one repeating unit. The most common and thermodynamically favored chemical transformations of alkenes are addition reactions.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_III_(Morsch_et_al.)/30%3A_Synthetic_Polymers/30.01%3A_Chain-Growth_PolymersPolymers resulting from additions to alkenes monomers are chain-growth polymers. In these processes each addition step results in a longer chain which ends in a reactive site. The mechanism of each ad...Polymers resulting from additions to alkenes monomers are chain-growth polymers. In these processes each addition step results in a longer chain which ends in a reactive site. The mechanism of each addition step is the same, and each addition step adds another monomer to extend the chain by one repeating unit. The most common and thermodynamically favored chemical transformations of alkenes are addition reactions.
- https://chem.libretexts.org/Workbench/Pick_Your_Poison%3A_Introduction_to_Materials_Toxicology/31%3A_Synthetic_Polymers/31.02%3A_Chain-Growth_PolymersPolymers resulting from additions to alkenes monomers are chain-growth polymers. In these processes each addition step results in a longer chain which ends in a reactive site. The mechanism of each ad...Polymers resulting from additions to alkenes monomers are chain-growth polymers. In these processes each addition step results in a longer chain which ends in a reactive site. The mechanism of each addition step is the same, and each addition step adds another monomer to extend the chain by one repeating unit. The most common and thermodynamically favored chemical transformations of alkenes are addition reactions.
- https://chem.libretexts.org/Workbench/LCDS_Organic_Chemistry_OER_Textbook_-_Todd_Trout/31%3A_Synthetic_Polymers/31.02%3A_Chain-Growth_PolymersPolymers resulting from additions to alkenes monomers are chain-growth polymers. In these processes each addition step results in a longer chain which ends in a reactive site. The mechanism of each ad...Polymers resulting from additions to alkenes monomers are chain-growth polymers. In these processes each addition step results in a longer chain which ends in a reactive site. The mechanism of each addition step is the same, and each addition step adds another monomer to extend the chain by one repeating unit. The most common and thermodynamically favored chemical transformations of alkenes are addition reactions.
- https://chem.libretexts.org/Courses/Williams_School/Chemistry_II/10%3A_Synthetic_Polymers/10.01%3A_Chain-Growth_Polymersand the other electron remains attached to the other alkene carbon. (Curved arrows with only one "barb" on a point are used to follow the path of a single electron in the same way that "double-headed"...and the other electron remains attached to the other alkene carbon. (Curved arrows with only one "barb" on a point are used to follow the path of a single electron in the same way that "double-headed" arrows follow the path of an electron pair.) Intermediates with an unpaired electron are called free radicals, so this step can be described as adding a free radical to an alkene to lengthen the chain by two carbons and generate a new free radical.
- https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/30%3A_Synthetic_Polymers/30.01%3A_Chain-Growth_Polymersand the other electron remains attached to the other alkene carbon. (Curved arrows with only one "barb" on a point are used to follow the path of a single electron in the same way that "double-headed"...and the other electron remains attached to the other alkene carbon. (Curved arrows with only one "barb" on a point are used to follow the path of a single electron in the same way that "double-headed" arrows follow the path of an electron pair.) Intermediates with an unpaired electron are called free radicals, so this step can be described as adding a free radical to an alkene to lengthen the chain by two carbons and generate a new free radical.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(OpenStax)/31%3A_Synthetic_Polymers/31.01%3A_Chain-Growth_PolymersPolymers resulting from additions to alkenes monomers are chain-growth polymers. In these processes each addition step results in a longer chain which ends in a reactive site. The mechanism of each ad...Polymers resulting from additions to alkenes monomers are chain-growth polymers. In these processes each addition step results in a longer chain which ends in a reactive site. The mechanism of each addition step is the same, and each addition step adds another monomer to extend the chain by one repeating unit. The most common and thermodynamically favored chemical transformations of alkenes are addition reactions.
