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- 2. For each of the following pair of reactions, CIRCLE the reaction that will occur faster (A or B). A A A H. 1 Br Br CH3ONa CH3OH NaCN ACN Nal DMSO B B B |||||| Br CI Br CH3ONa CH3OH NaCN ACN Nal DMSO3. In each blank, put the major product of the reaction. CH3 кон Br KOH OH H+ OH H+Draw the least stable resonance form the intermediate in the following electophilic substitution reaction.
- Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. LOCH3 LOCH3 HNO3 / CH3CO₂H O₂N • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. ● In cases where there is more than one answer, just draw one.10. Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction.3. Which of these two reactions would go better? Why? N2OH CH,CH;Br CH,CH,OH Br CH,CH, CH, NaOH он CH,CCH, CH,
- 6. Circle the product of the following reaction. 1. C=C-H 2. H2O НО Н H H3C . I H3C OH Н || Н сан Н Н.с о IV H НDraw the entire extended reaction mechanism (curly arrows) for this reaction но- OH HO HO OMe H OMe OMe HO HO OMeDraw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. (please show which structure I need to put as the answer).
- Please explain each choice.( do last 2 with mechanism )7. The reaction of methoxide anion with bromoethane to yield the ether ethyl methyl ether and the bromide anon (Br-) is an excellent example of a general reaction type called Sy2 (substitution nucleophilic bimolecular): CH,0+ CH,СH-Br a CH3-0-CH,СH; + Br- a. Change in enthalpy is -103 kJ/mol; the change in entropy is + 0.025 kJ/mol-K. Calculate DG at 300K. b. Is the reaction endergonic or exergonic? c. Is the reaction endothermic or exothermic? d. Use curved arrows to show the complete mechanism. Reaction of 2-methyl-1-butene with H-Cl could yield TWO alkyl chloride products. Draw and name 8. them.