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Description Reaction mechanism of the nucleophilic substitution of tert-butanol by hydrogen chloride. Step 2: Protonated tert-butanol loses H2O to form the tert-butyl cation, (CH3)3C+.
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Author Ben Mills
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Public domain This work has been released into the public domain by its author, Benjah-bmm27. This applies worldwide.

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1 December 2007

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current16:54, 1 December 2007Thumbnail for version as of 16:54, 1 December 20071,100 × 494 (28 KB)Benjah-bmm27{{Information |Description = Reaction mechanism of the nucleophilic substitution of tert-butanol by hydrogen chloride. Step 2: Protonated tert-butanol loses H<sub>2</sub>O to form the tert-butyl cation, (CH<sub>3</sub>)<sub>3</sub>C<sup>+</sup>. |Source =

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