Diels-Alder Reaction (Butadiene + Ethylene)

C4H6 + C2H4 → C6H10

अवलोकन

A conjugated diene (1,3-butadiene) reacts with a dienophile (ethylene) in a [4+2] cycloaddition to form cyclohexene. This pericyclic reaction proceeds through a concerted mechanism with no intermediates, forming two new carbon-carbon bonds and a six-membered ring simultaneously.

प्रतिभागी

भूमिका पदार्थ गुणांक अवस्था
अभिकारक Ethylene C₂H₄ 1 (g)
उत्पाद Cyclohexane C₆H₁₂ 1 (l)

रोजमर्रा का उदाहरण

Otto Diels and Kurt Alder won the 1950 Nobel Prize for discovering this reaction, which is taught in every organic chemistry course.

औद्योगिक महत्व

Diels-Alder reactions are used to synthesize steroids, terpenes, alkaloids, and many pharmaceutical intermediates with precise stereochemical control.

गुण

प्रकार
Organic
प्रतिवर्ती
हाँ
ऊर्जा
ऊष्माक्षेपी
ΔH
-40.0 kJ/mol

संबंधित अभिक्रियाएँ

Swern Oxidation Oxidation of Secondary Alcohol to Ketone Claisen Condensation (Ethyl Acetate) Kolbe Electrolysis Baeyer-Villiger Oxidation Beckmann Rearrangement (Cyclohexanone Oxime) Catalytic Hydrogenation of Ethylene Condensation Polymerization (Nylon 6,6) Cope Rearrangement Epoxidation of Alkenes (mCPBA)

Frequently Asked Questions

What is the equation for Diels-Alder Reaction (Butadiene + Ethylene)?
The balanced equation is: C₄H₆ + C₂H₄ → C₆H₁₀.
What type of reaction is Diels-Alder Reaction (Butadiene + Ethylene)?
Diels-Alder Reaction (Butadiene + Ethylene) is a organic reaction. It is reversible under certain conditions.
Is Diels-Alder Reaction (Butadiene + Ethylene) exothermic or endothermic?
Diels-Alder Reaction (Butadiene + Ethylene) is exothermic (releases energy). The enthalpy change (ΔH) is -40.0 kJ/mol.