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31. Catalysis in Organic Reactions - Part 2 of 2!
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31. Catalysis in Organic Reactions - Part 2 of 2!
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31. Catalysis in Organic Reactions / Intramolecular Nucleophilic Catalysis / Problem 12
Problem 12
In the ring-opening of asymmetrical epoxides under acidic conditions, why does the nucleophile attack the more substituted carbon?
A
Because the more substituted carbon is less electrophilic.
B
Because the more substituted carbon is more sterically hindered.
C
Because the more substituted carbon has a higher electron density.
D
Because the more substituted carbon is more positively charged in the transition state.
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