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Draw the major product of this SN1 reaction. Ignore any inorganic byproducts.
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- Phenols (ArOH) are relatively acidic, and the presence of a substituent group on the aromatic ring has a large effect. The pKa of unsubstituted phenol, for example, is 9.89, while that of p-nitrophenol is 7.15. Draw resonance structures of the corresponding phenoxide anions and explain the data.OB О А Question 5 Which of these would react with CrO3? О А OD ОВ О А O Cand D Ос ОН 38 О O A, C and D В с D ОН CH3 Mac4. Provide the products for the reactions. Take note of the changes and how they tie together for the overall result. Br NaNH2 H20 З еq Br Br NaNH2 2 eq Br Bгz 1. NANH2, 3 eq 2. H20 Он conc. H2SO4 Br2 1. NaNH2, 3 eq heat 2. Нао
- Which products are most likely to form in this reaction? NH2 H2N NaNH2 NH2 liq. NH3 II O1, II & II O II & II O1& || OI & IIProvide the products and detailed arrow pushing mechanisms for the following reactions: OSIME3 EtN CO.Me 1. base, dilute solution (10mM) 2. NaOH/MEOH-H,0 Acid, heat CO.Me14C 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 these
- 3. Provide the structure of the major product(s) for the following reaction. 4. Predict the product for the following reaction. OCH3 А) I В) II C) II D) IV E) V NBS Д OCH3 OCH3 || 32, N 100 atm, 100ºС OCH 3 ||| OCH3 IV OCH3V. Predict the major product of the following reactions. Draw and name the products. NaH 1. KMNO4 2. H,SO(aq) 3. room temp FOH H;SO, THE warm HBr 5.Predict the product(s) for the SN1 reaction shown. O II III O | O IV ○ I and IV O II and III OH2 || = OH HI III IV OH2