IB Chemistry R3.4 Electron pair sharing reactions in organic molecules
Автор: Heather Lentz
Загружено: 2025-02-02
Просмотров: 869
Описание:
Nucleophilic substitution and electrophilic addition reactions
Understandings
R3.4.1 A nucleophile is a reactant that forms a bond to its reaction partner (the electrophile) by donating both bonding electrons.
R3.4.2 In a nucleophilic substitution reaction, a nucleophile donates an electron pair to form a new bond, as another bond breaks producing a leaving group.
R3.4.3 Heterolytic fission is the breakage of a covalent bond when both bonding electrons remain with one of the two fragments formed.
R3.4.4 An electrophile is a reactant that forms a bond to its reaction partner (the nucleophile) by accepting both bonding electrons from that reaction partner.
R3.4.5 Alkenes are susceptible to electrophilic attack because of the high electron density of the carbon-carbon double bond. These reactions lead to electrophilic addition.
Повторяем попытку...
Доступные форматы для скачивания:
Скачать видео
-
Информация по загрузке:
![Electron-pair Sharing Reactions [IB Chemistry SL/HL]](https://ricktube.ru/thumbnail/ntJIMbTYCJA/mqdefault.jpg)
![R3.4.11 Electrophilic Addition to Alkenes [HL IB Chemistry]](https://ricktube.ru/thumbnail/5a4ZJPeo2bY/mqdefault.jpg)
![R3.4.9 Stereoinversion in Sn2 reactions [HL IB Chemistry]](https://ricktube.ru/thumbnail/wPxO0zmYKtQ/mqdefault.jpg)
![IB Biology C1.1 - Enzymes & Metabolism [SL/HL] - Interactive Lecture 2025-2033](https://ricktube.ru/thumbnail/WphDfJ87Css/mqdefault.jpg)
![Electron Transfer Reactions [IB Chemistry SL/HL]](https://ricktube.ru/thumbnail/9oop0c8yzgg/mqdefault.jpg)
