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30.10: A Summary of Rules for Pericyclic Reactions

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    448886
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    How can you keep straight all the rules about pericyclic reactions? The summary in Table 30.1, Table 30.2, and Table 30.3 can be distilled into a mnemonic phrase that provides an easy way to predict the stereochemical outcome of any pericyclic reaction:

    The Electrons Circle Around (TECA)

    Thermal reactions with an Even number of electron pairs are Conrotatory or Antarafacial.

    A change either from thermal to photochemical or from an even to an odd number of electron pairs changes the outcome from conrotatory/antarafacial to disrotatory/suprafacial. A change from both thermal and even to photochemical and odd causes no change because two negatives make a positive.

    These selection rules are summarized in Table 30.4; knowing them gives you the ability to predict the stereochemistry of literally thousands of pericyclic reactions.

    Table 30.4 Stereochemical Rules for Pericyclic Reactions
    Electronic state Electron pairs Stereochemistry
    Ground state (thermal) Even number
    Odd number
    Antara–con
    Supra–dis
    Excited state (photochemical) Even number
    Odd number
    Supra–dis
    Antara–con

    Predict the stereochemistry of the following pericyclic reactions:

    1. The thermal cyclization of a conjugated tetraene
    2. The photochemical cyclization of a conjugated tetraene
    3. A photochemical [4 + 4] cycloaddition
    4. A thermal [2 + 6] cycloaddition
    5. A photochemical [3,5] sigmatropic rearrangement

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