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Top Questions
13
votes
Why does a hydride like NaH act as a base, but a hydride like NaBH4 act as a nucleophile?
organic-chemistry
reaction
asked May 7, 2015 at 0:41
chemistry.stackexchange.com
8
votes
Why can you not make a compound with a quaternary alpha carbon using malonic ester?
organic-chemistry
synthesis
esters
asked Apr 10, 2015 at 7:00
chemistry.stackexchange.com
7
votes
In the Haworth projections of D and L glucose, is the stereochemistry at every carbon except the anomeric carbon just inverted?
organic-chemistry
stereochemistry
carbohydrates
asked May 5, 2015 at 3:22
chemistry.stackexchange.com
5
votes
Why are esters meta directors? Can't the carbonyl donate electrons into the ring?
organic-chemistry
aromatic-compounds
stability
asked Apr 28, 2015 at 5:08
chemistry.stackexchange.com
Top Answers
No answers with score of 5 or more
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