why can't you do an ir spectrum or melting point of the product tetraphenylcyclopentadienone being synthesized from benzil and 1,3-diphenylacetone?
why can't you do an ir spectrum or melting point of the product tetraphenylcyclopentadienone being synthesized from benzil and 1,3-diphenylacetone?
Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter8: Haloalkanes, Halogenation, And Radical Reactions
Section: Chapter Questions
Problem 8.11P
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why can't you do an ir spectrum or melting point of the product tetraphenylcyclopentadienone being synthesized from benzil and 1,3-diphenylacetone?
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