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6.4: Acid-Catalyzed Hydration

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    321426
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    A slight variant of the electrophilic addition of H-X across a double bond is the acid-catalyzed addition of H2O across a double bond, also known as an acid-catalyzed hydration. The mechanism has a few key differences, but overall looks quite similar.

    The first step is protonation of the alkene (by H2SO4) at the less highly substituted carbon to give the more highly substituted (thus, more stable) carbocation. In the next step, the nonbonding pair of electrons on H2O will act as a nucleophile to attack the empty atomic p orbital on carbon. When this happens, a bond forms between the oxygen and the carbon. This species is overall positively charged. To get rid of the charge, remember that protons can be removed (or added) very easily. Thus, proton transfer occurs. Some weak base (either H2O or HSO4) can attack the proton via its \(σ^{*}_{H-O}\) orbital, breaking the \(σ_{H-O}\) bond and moving the electrons up onto oxygen as a lone pair. The net result is the regeneration of the acid (hence, why it’s a catalyst) and the formation of the alcohol product.

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    Synthesis

    You are now at a point where you can begin to make molecules of greater complexity. So far, you have a simple starting material (an alkene) that can be reacted with two different types of reagents (H-X or H2SO4/H2O) to give two different functional groups (alkyl halide and alcohol, respectively. The mechanism is exactly the same for this reaction – electrophilic addition. You should now be comfortable enough to draw the mechanism for both reactions, but also be able to predict the product, reagents, or starting materials of this transformation when the other two are provided. This will be a common theme as we work through more and more reactions.

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    6.4: Acid-Catalyzed Hydration is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by LibreTexts.

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