<span>c. Passing electric charge through the reactants Is the answer to you're question.
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Answer:
Explanation:
Diels-Alder reactions are cyclo-additional reactions between conjugated dienes and a dienophile (a substituted alkene compound for example acrylic acid) to produce a ring structure of cyclohexene compounds.
From the image attached below, we will see the reaction between 2,3-dimethylbuta-1,3-diene which is a conjugated diene with acrylic acid to produce a Diel-Alder adduct as the product. From the reaction, a single new π-bond and two σ-bonds are produced.
Answer:
V=20.2m3
Explanation:
P= 225.4kPa V= ? n= 1.85, T= 22.5+273= 295.5K, R = 8.314
Applying the ideal gas equation
PV=nRT
225.4×V = n×8.314×295.5
V= 20.2m3