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.) ere are several regio- and stereochemical questions to be considered here: Is the conformation of the diene s-cis or s-trans? How will the dienophile be oriented relative to the diene? (In the product will the electron-withdrawing ester group of the dienophile be "ortho", "mete", or "para" to the electron-donating methyl group of the diene?) Is there a chirality center in the product? Where is it?
