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- The following reactions are unlikely to provide the indicated product in high yield. What is wrong with each?When a 2, 6-disubstituted allyl phenyl ether is heated in an attempted Claisen rearrangement, migration occurs to give the p-allyl product as the result of two sequential pericyclic reactions. Explain.Melamine, used as a fire retardant and a component of the writing surface of white boards, can be prepared from s-trichlorotriazine through a series of SNAr reactions with ammonia. The first substitution takes place rapidly at room temperature. The second substitution takes place near 100 °C, and the third substitution requires even higher temperature and pressure. Provide an explanation fatr this reactivity.
- ab provide d remo gy nthesi's ANDA Forcward Synthesi s for the fouowing tano Foma ton from the provided startung matenon (some of whos e carbon atoms mustbe Integrated into the pro duct -i.eyou can't sust draw the produet as the Other reagens. Mather reagent and any. 'NO mechandsms required: Br BrWhat starting materials are needed to synthesize each azo compounds O2N H2N- -N=N- CI но -N=N- -CH3 I0 Fill in the reagent or starting material needed or product in each reaction a) CgH;CH;CH;CH2Br CGH;CH;CH;CH¿NH2 b) C,H;CH;CH;CH2CONH, CH,CH;CH;CH;NH2 HCI P-CH;C,H4NH2 NANO2 P-CH;C,H&NH2 HCI/H;0 P-CH3C,H4NH2 CH;COCI4) Give the correct product with the correct stereochemistry. Me Me 5) Give the major product. hv HCI OC
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