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- PaylbenWhat diene and dienophile are used in the Diels-Alder route to the compound shown? "CO,CH Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. T NV H± 12D EXP CONT ? K H CI CNO SUB Br MDraw the structure of the product of the Diels-Alder reaction below. O || H3C CH3 O + CH3OC-C=C-COCH3
- Draw the TWO possible products of the Diels-Alder reaction shown below.Which of the following would be the most reactive in a Diels-Alder [4+2] cycloaddition as the diene? 0000 2 = = - IV || ||| IV5.- Retro Diels-Alder: show a combination of diene and dienophile that would result in each Diels-Alder adduct. a) b) c) H3C. CHO '' CHO CN CN miwoll
- Rank the dienes by DECREASING REACTIVITY in Diels-Alder reactions (most reactive on the left). CN CH3 OCH3 II II IV O A. V > IV > || > | > || O B. V > || > NIl > | > IV O C. IV > T > I| > ||| > V O D. II > |II > V >[ > ]V O E. V > III > I|| > | > IV A Moving to another question will save this response. ype here to searchIdentify the diene and dienophile expected to produce the Diels-Alder product shown in the box below. SO 11 SO IV ον O. IV 4 ||| ||| ||Finish the reaction by drawing the initial Diels-Alder product. H3C CH3 H₂C CH3 H CH
