Nucleophillic acyl substitutions go through a trigonal planar intermediate.
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Q50: Dimethylaminopyridine is a better catalyst than pyridine
Q51: Dicyclohexylcarbodiimide is a reagent used to form
Q52: A Grignard reaction will reduce an ester
Q53: Acid chlorides are less electrophilic then acid
Q54: Electron withdrawing groups make an aromatic ring
Q56: The tetrahedral intermediate is the result of
Q57: DIBAL can reduce acid anhydrides into both
Q58: Borane can reduce an amide to either
Q59: An acyl chloride can be reduced by
Q60: Esters are more electrophilic then amides.
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