The concept used to solve this problem is based on Diel’s-Alder reaction.
The Diel’s-Alder reaction is a reaction between a diene and a dienophile in the presence of heat or light. In this reaction, a conjugated diene reacts with an alkene which is called a dienophile to form a [4+2] cycloaddition compound in the presence of heat or light.
This reaction is a pericyclic reaction. The cycloaddition between a diene and an alkene or substituted alkene occurs in a concerted manner that is, in a single step to form the final product.
The diene and dienophile are shown as follows:
The [4+2] cycloaddition occurs as follows:
Ans:The product formed is as follows:
Draw one enantiomer of the major product of the following Diels? Alder reaction. (Use wedge/dash bonds...
Draw one enantiomer of the major product of the following Diels-Alder reaction. (Use wedge/dash bonds to indicate the orientation of substituents in the product. Hydrogen atoms on chirality centers must be shown explicitly.)
Draw one enantiomer of the major product of the following Diels-Alder reaction (Use wedge/dash bonds to indicate the orientation of substituents in the product. Hydrogen atoms on chirality centers must be shown explicitly.)
Draw one enantiomer of the major product of the following Diels- Alder reaction. (Use wedge/dash bonds to indicate the orientation of substituents in the product. Hydrogen atoms on chirality centers must be shown explicitly.)
Draw one enantiomer of the major product of the folllowing Diels- Alder reaction. (Use wedge/dash bonds to indicate the orientation of substituents in the product. Hydrogen atoms on chirality centers must be shown explicitly.)
Draw one enantiomer of the major product of the folllowing Diels-Alder reaction. (Use wedge/dash bonds to indicate the orientation of substituents in the product. Hydrogen atoms on chirality centers must be shown explicitly.)
Draw one enantiomer of the major product of the folllowing Diels-Alder reaction. (Use wedge/dash bonds to indicate the orientation of substituents in the product. Hydrogen atoms on chirality centers must be shown explicitly.)
Draw one enantiomer of the major product of the folllowing Diels%u2013Alder reaction. (Use wedge/dash bonds to indicate the orientation of substituents in the product. Hydrogen atoms on chirality centers must be shown explicitly.) ?
Draw one enantiomer of the major product of the following Diels–Alder reaction. Use wedged/hatched bonds to indicate the orientation of substituents in the product. Chirality centers must contain four bonds in order to be graded correctly. Hydrogen atoms on chirality centers must be shown.
Draw one enantiomer of the major product of the following Diels-Alder reaction. Use wedged/hatched bonds to indicate the orientation of substituents in the product. Chirality centers must contain four bonds in order to be graded correctly. Hydrogen atoms on chirality centers must be shown. solution of a specific vitamin has λmax = 257 nm and a concentration of 3.69 10-7 M. The absorbance of the solution at 257 nm is A = 0.185. What is the molar absorptivity of the vitamin...
Draw the product(s) of the Diels–Alder reaction of 1,3-butadiene with trans-1,2-dibromoethene. Use wedge-and-dash bonds to show the stereochemistry of the product(s). Include hydrogens at any chirality centers.