Chemistry
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Can you answer the question and explain it? With the mechanism 

Only e and f

 

 

**Predict the products for the following reactions:**

(a) Benzene + Malononitrile

(b) Furan + Acetaldehyde

(c) Propanenitrile + Benzene

(d) 3,4-Dimethoxythiophene

(e) (Z)-Butenedioic acid + Furan

(f) Acrylonitrile + Furan

Each of these reactions involves different organic compounds, and the task is to predict the potential products formed as a result of these chemical reactions. The structures and formulas indicate typical reactants used in organic chemistry involving aromatic compounds, nitriles, and carbonyls.
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Transcribed Image Text:**Predict the products for the following reactions:** (a) Benzene + Malononitrile (b) Furan + Acetaldehyde (c) Propanenitrile + Benzene (d) 3,4-Dimethoxythiophene (e) (Z)-Butenedioic acid + Furan (f) Acrylonitrile + Furan Each of these reactions involves different organic compounds, and the task is to predict the potential products formed as a result of these chemical reactions. The structures and formulas indicate typical reactants used in organic chemistry involving aromatic compounds, nitriles, and carbonyls.
Expert Solution
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Step 1 Theory

Diels-Alder reaction: It is a [4+2] cycloaddition reaction between a diene and dienophile to give a six membered cyclic product. 

It is a no mechanism reaction. The reaction takes place in a single, concerted step.

Diene must be electron rich and dienophile must be electron deficient.

 

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