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- The following reaction has a ΔSsystem < 0 O2(g) → 2O(g) T or F can you explain why this is false?6. Identify the best reagent(s) for this reaction. (see attached screenshot). a. H2SO4, HgSO4, H2O b. 1. Disiamylborane, 2. HO–, H2O2 c. K2Cr2O7, H+ d. NaOCl e. H2, PdWrite the expected product for each of the following reactions: Diphenyl sulfide + 1 eq. NaOCl -------------> ? 1,2-Epoxy-3,3-dimethylbutane + 1 eq. CH3CH2SNa then CH3Br -------------> ? 1,2-Epoxy-3-phenylpropane + HCl ------------> ?
- Choose the answer that best represents the products of the following reaction. Potassium carbonate is reacted with phosphoric acid. A. 2 K3PO4 (aq) + 3 H2O (l) + 3 CO2 (g) B. K2CO3 + H3PO4 C. 3 K2CO3 + 2 H3PO4 D. 2 K3PO4 (aq) + 3 H2CO3 (aq)Thank you for the answer, would it be possible to follow the path I have attached as well srarting from methanol ---> CH3Br -----> CH3MgBr-------> (H3C)CH-CH2OH ----> E1 IsobutaleneGive the name/s only (structures not required) of the product for the reaction of (i) A and (ii) B with the reagents listed below. Your answers should be given using A1 -A10 and B1-B10 as indicators.Eg. the product for your first reaction should be stated as A1 = name of product etc. b2h6/h202 n-bromosuccinimide kmno4/oh-
- select the most appropriate reagent(s) to effect the change. K2Cr2O7, H+ H2, Pd 1. Disiamylborane, 2. HO–, H2O, H2O2 NaOCl H2SO4, HgSO4What is the product of the reaction P4O6 + H2O? A) H3PO4 B) H2PO4 C) H3PO3 D) H2PO3 E) H2P4O7Match the questions with the correct descriptions below: Sn2, E2 E1cb Sn1, E1 (anti) E2, E1cb Sn1, E1 2 steps poor leaving group 2 carbons removed from a carbonyl group carbanion intermediate 3°>allylic, benzylic>2°>1°>CH₃ carbocation intermediate Ist order reaction (r=k[RX]) H-X anti no intermediate 2nd order reaction (r=k[RX][Nu]) polar aprotic solvent
- Consider the series of the trans effect: CO, CN-, C2H4 > PR3, H-, CH3- > C6H5- > NO2-, SCN-, I- > Br- >Cl- > py > NH3 > H20 What would be the major product of the following reaction? Select one:3. What is the main product for each of the following reactions? (a) p-Methylanisole + CH3CH2COCl, AlCl3 --------> ? (b) Toluene + Br2, light, then CH3CH2COCl, AlCl3 --------> ? (c) Acetophenone + CH3CH2Cl, AlCl3, then Br2, Fe -----> ? (d) Styrene + CH3CH2COCl AlCl3, then Br2, Fe -----> ? (e) Benzene + 1-chloro-2,2-dimethylpropane, AlCl3 -----> ? (f) Benzene + HCOCl, AlCl3 then 1-chlorobutane, AlCl3 -----> ? 4. Using arrows to show electron movement, write the stepwise mechanism for the major products in the reactions (3a and 3f) listed above.Draw the organic product formed for each reaction. e. CI & COOH COOHfallization of A COOH [1] LDA [2] CH3CH₂I [1] Br₂, CH3CO₂H [2] Li₂CO3, LiBr, DMF 1₂ (excess) TOH -aminopher should you use NaHnimm CN to the Büchn Br₂ (excess) -OH ydride to form ace + CHI3 rinse the task wh