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- Show how to Synthusize fon benzene and neassoy reogentsClassify the following reactions as oxidation, reduction, or “not redox”, depending on whathappens to the starting material. Explain your reasoning in each case.Write cibout high) knd low and Their acdiatanles and disedientris ds well as density pelyethhine Application:
- 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.ences] Use the References to access important values if needed for this question. Draw the organic product that is expected to form when the following compound is oxidized under biological conditions. oxidation CH,CH,SH reduction • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If no reaction occurs, draw the organic starting material. C. opy aate Pre ChemDoodle"(b) How can be prepared from OEt CO,Et and at EtO OEt EtO2C 95 °C ? Provide the mechanism.
- Shaw haw T compaunds YOIC a.Smm cauld prepare the fallauing materials with the starting shawn and ather any inarganie reagende necessarg arganic ar Jo HINT Yo ill peed EN do to allylic hreminatian an92/ Outline all steps in a possi ble laboratory Synthesis Gamo of te following Commpounds: (using any inarganic or organic reagents ) A cetylene GM) from a) 3-hexyneWhich type of reaction – addition, elimination, rearrangement, substitution,- best describes each of the following? OLi (а) MeLi + Me H (Б) Me2NOH + (c) to (d) H2O -ОН +
- In cells, vitamin C exists largely as its conjugate base X. X is anantioxidant because radicals formed in oxidation processes abstract thelabeled H atom, forming a new radical that halts oxidation. Draw thestructure of the radical formed by H abstraction, and explain why this Hatom is most easily removed.16) Synthesize: From: prop-2-enol and propeneHow to prepare dicyclopentylether from cyclopentene??