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- For each of the tolowing reactions predict the major product. NaOH H,0, A Raney N. A préssure OH H,Cro, H,S0, H,0 Proposea forwad sythesis or ene of the two seences below using whateve agents necessary. Do not indude any ourvedamow mechanisms, just the reactions OH OH ORDraw the predicted major products of the following reactions. Ph OHC., (PhP);RhCI PHCN, A H,CCH, Grubbs I, CH,OCl, Rh(CO),CI CO R-0 B(OH)2 Pd(OAc)2 K3PO4 Pd(OAc)2 K3PO4What is the predicted product of the reaction shown? ОТ O II O ||| O IV OV Н Na2Cr2O7/H2SO4/H2O IV || ОН ОН овог H V Ш OH ОН
- Clear my choice Which of the following is/are the expected product/s of the reaction of 2-pentanone (CH3COCH CHACH) with excess Bro, followed by OHT? O CHCOCHBRCH,CH3 BICH,COCH2CH;CHa O CHBr + CH,CH,CH,COO OCHBR + CH,CH,CH,COOH Which compound can undergo Cannizzaro reaction? CH,CHOProvide the major organic product of the reaction shown. NV L Draw the molecule on the canyas by choosing buttons from the Tools (for bonds), t [1] A OH 4' 1. NaH эсе 2. CH₂CH₂CH₂CH₂I H: 120 EXP. CONT L Marvin JS ? ** I U ZOS CI BrChapter 8 Problem 166 Draw all likely alkene products in the following reaction. NN [1] Br "n CH3 Draw the molecules on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Submit A NaOH U acetone Request Answer 1 H 12D EXP CONT: ● ● Marvin JS by ChemAxon DA H C N O S CI Br I P F
- NaOMe MeOH A B D E F What are the two starting materials? of14C labelled OTS RCO H 16. →product; Product of this reaction is : no label ОCOR OCOR (a) (b) (c) both (a) and (b) (d) None of theseH9.23 - Level 2 Unanswered • 3 attempts left What is the major product formed in the following reaction? A A В D D E H;SO. (conc.) OH heat oso;H D
- 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.Explain why ethene does not react with HX ( X=Cl , Br or I) under normal conditions.The following reactions are unlikely to provide the indicated product in high yield. What is wrong with each?
