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?

C₂H₂C=0
|
CH,C=O
Benzil
MW 210.22
mp 96°C
C6H5
1
CH₂
C=O
C6H₂CH₂N*(CH3)3OH¯
- 2 H₂O
/
CH₂
T
C6H5
1,3-Diphenylacetone
MW 210.26
mp 35°C
C₁Hs
C6H,
C6H5
C=O
C₂H₁
Tetraphenylcyclopentadienone
MW 384.45 mp 219°C
Transcribed Image Text:C₂H₂C=0 | CH,C=O Benzil MW 210.22 mp 96°C C6H5 1 CH₂ C=O C6H₂CH₂N*(CH3)3OH¯ - 2 H₂O / CH₂ T C6H5 1,3-Diphenylacetone MW 210.26 mp 35°C C₁Hs C6H, C6H5 C=O C₂H₁ Tetraphenylcyclopentadienone MW 384.45 mp 219°C
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