Experiment: Synthesize of 1,5-diphenyl-(E,E)-1,4-pentadien-3-oneNaOH, H,оEt-OH1,5-Diphenylpenta-1,4-dien-3-oneBenzaldehydeC17H140C7H60Mol.wt:234.29Mol.Wt:106.12Things to consider:-Identify the moles of each reactant used.-Considering the aldol reaction and its mechanism, write a possible reaction mechanism for this reaction-What would be the amounts of same reactants required to obtain E-4-phenylbut-3-en-2-one?-Write the structure of the product that you would obtain if you replace benzophenone with benzaldehydeassume that the moles of benzophenone is equal to the moles of benzaldehyde in the reaction proceduregiven above.2.

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Experiment: Synthesize of 1,5-diphenyl-(E,E)-1,4-pentadien-3-one NaOH, H,0 Et-OH 1,5-Diphenylpenta-1,4-dien-3-one Benzaldehyde C17H140 C7H60 Mol.wt:234.29 Mol.Wt:106.12 Things to consider: -Identify the moles of each reactant used. -Considering the aldol reaction and its mechanism, write a possible reaction mechanism for this react -What would be the amounts of same reactants required to obtain E-4-phenylbut-3-en-2-one? -Write the structure of the product that you would obtain if you replace benzophenone with benzaldel assume that the moles of benzophenone is equal to the moles of benzaldehyde in the reaction procedu given above.

Experiment: Synthesize of 1,5-diphenyl-(E,E)-1,4-pentadien-3-one NaOH, H,0 Et-OH 1,5-Diphenylpenta-1,4-dien-3-one Benzaldehyde C17H140 C7H60 Mol.wt:234.29 Mol.Wt:106.12 Things to consider: -Identify the moles of each reactant used. -Considering the aldol reaction and its mechanism, write a possible reaction mechanism for this react -What would be the amounts of same reactants required to obtain E-4-phenylbut-3-en-2-one? -Write the structure of the product that you would obtain if you replace benzophenone with benzaldel assume that the moles of benzophenone is equal to the moles of benzaldehyde in the reaction procedu given above.

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

Chapter20: Dienes, Conjugated Systems, And Pericyclic Reactions

Section: Chapter Questions

Problem 20.24P: Pyridine exhibits a UV transition of the type n at 270 nm. In this transition, one of the unshared...

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