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- Writing Linear Structures
- Primary, Secondary and Tertiary Hydrogen Atoms
- The Products of an Elimination Reaction
- Products of Elimination: Zaitsev's Rule
- The E1 Mechanism
- Products of Elimination: Zaitsev's Rule Q1
- The E2 Mechanism
- Simultaneous E and SN Reactions
- Products of Elimination: Zaitsev's Rule Q2
- Electrophilic Addition Reactions
- Relative Rates of Elimination and Substitution
- Electrophilic Addition: Markovnikoff Rule
- Markovnikoff Rule Questions
Elimination and Electrophilic Addition
Two kinds of reaction are possible when a nucleophilic reagent attacks a substituted alkane. In nucleophilic substitutions the nucleophile displaces a weaker nucleophile from its bonded site. In elimination reactions, the nucleophile removes a Hydrogen from a neighbouring C-atom and causes elimination of the leaving group leading to the formation of an alkene. The reagents and conditions determine which reaction predominates. In this module, we will also present the key features of addition reactions, where electrophilic reagents interact with electron rich multiple bonds.