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Calculate the theoretical yield and percent yield. Reaction between 2.0g Tetraphenylcyclopentadienone and 0.53 Maleic Anhydride with 5.0mL of bromobenzene to make Tetraphenyldihydrophthalic Anhydride. The yield obtained was 1.95g.

Calculate the theoretical yield and percent yield. Reaction between 2.0g Tetraphenylcyclopentadienone and 0.53 Maleic Anhydride with 5.0mL of bromobenzene to make Tetraphenyldihydrophthalic Anhydride. The yield obtained was 1.95g.

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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
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Calculate the theoretical yield and percent yield.

Reaction between 2.0g Tetraphenylcyclopentadienone and 0.53 Maleic Anhydride with 5.0mL of bromobenzene to make Tetraphenyldihydrophthalic Anhydride.

The yield obtained was 1.95g. 

 

 

The image depicts a chemical reaction involving organic molecules, specifically focused on the formation of a new compound through a reaction between two reactants. **Reactants:** 1. The first reactant is a five-membered aromatic ring known as a phenyl-substituted ketone. It is characterized by three phenyl groups (Ph) attached to the unsaturated ring structure. 2. The second reactant is maleic anhydride, a five-membered ring with two carbonyl groups (C=O) and one double bond. **Product:** - The primary product is a six-membered ring compound containing two ketone (C=O) groups. The ring is a result of the Diels-Alder reaction, incorporating the phenyl groups as substituents. **Byproduct:** - Carbon monoxide (CO) is released as a byproduct of the reaction. This transformation represents a typical Diels-Alder reaction, which is a common method for forming six-membered rings in organic chemistry with high efficiency and selectivity. The arrow indicates the direction of the reaction from reactants to products.
Transcribed Image Text:The image depicts a chemical reaction involving organic molecules, specifically focused on the formation of a new compound through a reaction between two reactants. **Reactants:** 1. The first reactant is a five-membered aromatic ring known as a phenyl-substituted ketone. It is characterized by three phenyl groups (Ph) attached to the unsaturated ring structure. 2. The second reactant is maleic anhydride, a five-membered ring with two carbonyl groups (C=O) and one double bond. **Product:** - The primary product is a six-membered ring compound containing two ketone (C=O) groups. The ring is a result of the Diels-Alder reaction, incorporating the phenyl groups as substituents. **Byproduct:** - Carbon monoxide (CO) is released as a byproduct of the reaction. This transformation represents a typical Diels-Alder reaction, which is a common method for forming six-membered rings in organic chemistry with high efficiency and selectivity. The arrow indicates the direction of the reaction from reactants to products.
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