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AnSwer the föllówing questions suing the reaction presented below: 2 Elend acetona beneal dehido di benza lacetona 1. Is there evidence that in the product there's only one geometric isomer (trans, trans) or there are an isomer mix in the product? The fusion point will help us answer this question? If so, explain. 2. How will change the process if wedesire to synthesize benzalacetofenone instead of dibenzalacetone? What reagents will need to be used to obtain this product? benzalacetofenona

AnSwer the föllówing questions suing the reaction presented below: 2 Elend acetona beneal dehido di benza lacetona 1. Is there evidence that in the product there's only one geometric isomer (trans, trans) or there are an isomer mix in the product? The fusion point will help us answer this question? If so, explain. 2. How will change the process if wedesire to synthesize benzalacetofenone instead of dibenzalacetone? What reagents will need to be used to obtain this product? benzalacetofenona

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Answer the following questions suing the reaction presented below: Elendl acetona benzal dehido di benza la cetona 1. Is there evidence that in the product there's only one geometric isomer (trans, trans) or there are an isomer mix in the product? The fusion point will help us answer this question? If so, explain. 2. How will change the process if wergesire to synthesize benzalacetofenone instead of dibenzalacetone? What reagents will need to be used to obtain this product? benzalacetofenona
Transcribed Image Text:Answer the following questions suing the reaction presented below: Elendl acetona benzal dehido di benza la cetona 1. Is there evidence that in the product there's only one geometric isomer (trans, trans) or there are an isomer mix in the product? The fusion point will help us answer this question? If so, explain. 2. How will change the process if wergesire to synthesize benzalacetofenone instead of dibenzalacetone? What reagents will need to be used to obtain this product? benzalacetofenona
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