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7.9: Elimination Reactions- Zaitsev's Rule

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  • Objective

    After completing this section, you should be able to apply Zaitsev’s rule to predict the major product in a base-induced elimination of an unsymmetrical halide.

    Key Terms

    Make certain that you can define, and use in context, the key term below.

    • Zaitsev’s rule


    Zaitsev's Rule can be used to predict the regiochemistry of elimination reactions.


    Zaitsev’s or Saytzev’s (anglicized spelling) rule is an empirical rule used to predict regioselectivity of 1,2-elimination reactions occurring via the E1 or E2 mechanisms. It states that in a regioselective E1 or E2 reaction the major product is the more stable alkene, (i.e., the alkene with the more highly substituted double bond). For example:

    If two or more structurally distinct groups of beta-hydrogens are present in a given reactant, then several constitutionally isomeric alkenes may be formed by an E2 elimination. This situation is illustrated by the 2-bromobutane and 2-bromo-2,3-dimethylbutane elimination examples given below.

    2-bromobutane reacts with alcochol and KOH. 20% of the products ar 1-butene and 80% of the products are 2-butene.  1-bromo-2-3-dimethylbutane reacts with alcohol and KOH. 21% of the products are 1,3-dimethyl-1-butene. 79% of the products are 2,3-dimethyl-2-butene.

    By using the strong base hydroxide, we direct these reactions toward elimination (rather than substitution). In both cases there are two different sets of beta-hydrogens available to the elimination reaction (these are colored red and magenta and the alpha carbon is blue). If the rate of each possible elimination was the same, we might expect the amounts of the isomeric elimination products to reflect the number of hydrogens that could participate in that reaction. For example, since there are three 1º-hydrogens (red) and two 2º-hydrogens (magenta) on beta-carbons in 2-bromobutane, statistics would suggest a 3:2 ratio of 1-butene and 2-butene in the products. This is not observed, and the latter predominates by 4:1. This departure from statistical expectation is even more pronounced in the second example, where there are six 1º-beta-hydrogens compared with one 3º-hydrogen. These results point to a strong regioselectivity favoring the more highly substituted product double bond, an empirical statement generally called the Zaitsev Rule.




    Ignoring the alkene stereochemistry show the elimination product(s) of the following compounds:



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