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    Organic Chemistry: Sn1E1 Reactions

    Chemistry

    • Title Home
    • Study Guide
    • Topics
      • SN1 and E1 Reactions
      • SN1 and E1 Reactions
      • Problems
      • Consequences of the Carbocation Intermediate
      • Carbocation Consequence Problems
    • Terms

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    Organic Chemistry: Sn1E1 Reactions Terms

    Terms

    Organic Chemistry: Sn1E1 Reactions Terms
    • Bimolecular

      Involving two molecules. In this SparkNote, the term bimolecular is used to refer to SN2 and E2 reactions. The rate-limiting transition states of both reactions involve two molecules.

    • Carbocation

      A carbon that carries a positive charge. Carbocations are highly unstable and are prone to rearrangement. SN1 and E1 reactions proceed through a common carbocation intermediate.

    • E1

      A reaction where a β-hydrogen is Eliminated to form a double bond. E1 reactions go through a carbocation intermediate. Somewhat similar to the E2 reaction.

    • SN1

      A reaction in which a Nucleophile Substitutes for a leaving group. SN1. It goes through a carbocation intermediate.

    • Secondary

      A secondary carbon has bonds to two other carbons.

    • Tertiary

      A tertiary carbon has bonds to three other carbons.

    • Unimolecular

      Involving one molecule. This term is used synonymously with the E1 and SN1 reactions in this SparkNote. The rate-limiting transition states of both mechanisms involve one molecule.

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