Chemistry
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user15437
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question
13
Why does a hydride like NaH act as a base, but a hydride like NaBH4 act as a nucleophile?
May 7, 2015
question
8
Why can you not make a compound with a quaternary alpha carbon using malonic ester?
Apr 10, 2015
question
7
In the Haworth projections of D and L glucose, is the stereochemistry at every carbon except the anomeric carbon just inverted?
May 5, 2015
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4
Why are esters meta directors? Can't the carbonyl donate electrons into the ring?
Apr 28, 2015
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Why are alpha-carbonyl relatively less stable?
Apr 8, 2015

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