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two-step method involving an SN2 attack of an alkoxide on an unhindered primary halide or tosylate
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- 80) Which of the following compounds would undergo autoxidation most readily?A) dibenzyl etherB) MTBEC) diethyl etherD) isobutyl phenyl ether
- in equilibrium with its hydrate, a geminal diol. The rxn is slow, but can be catalyzed
- around 4.5, too acidic and the amine will all be protonated (non-nucleophilic), too basic and the carbinolamine won't be protonated