PCC oxidation of a primary alcohol results in a carboxylic acid.
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Q49: E2 eliminations are susceptible to carbocation rearrangements.
Q50: Bromine acts as an electrophile in the
Q51: E1 eliminations go through a carbocation intermediate.
Q52: Heat promotes an E1 reaction over an
Q53: Dehydrohalogenation reactions can proceed under an E1
Q55: Sodium Hydride is an example of a
Q56: E2 reactions are promoted by protic solvents.
Q57: E1 reactions are usually less stereoselective than
Q58: An E1 mechanism occurs through a single
Q59: A strong bulky nucleophile will promote an
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