Provide the structure of the major organic product in the reaction below. H w 1. CHI (excess) CH3 2. Ag₂O 3. A Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template to + 12D 1
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- 2) Write the major products A- P for each of the following reactions. (70 point) HBr CH,CH,OK* CH;CH,OH t-BuO'K a) Br t-BUOH Br,/ H20 F Br KMNO/ OH Zn 1) 0, 2) Zn/ CH;COOH b) Br NANH, CH,CH,I H. Li NH; -78°C d) A concd. H,SO, L. H,O/ H Br, CCl, excess NaNH, hear NH,The product of the following reaction is: (Nat, CN-)/ ACETONE H. H. Br CI NC H- H. Br 1 CI CI CN CN II II 50% I & 50%|| IIAcetone (A) ; Major product of this reaction is : (major) 7. H. _F+ NaI (1 mole) Br (а) Н. .F (b) I- .F (с) Н. (d) H- H. H' Br Br
- 08:12 r ||| 3. The final product is removed from the organic layer by extraction with the hydrochloric acid solution. Draw the curved arrows for the proton transfer reaction that takes place, and draw the resulting product. Explain how this reaction enables the removal of the lidocaine from the organic layers. dr organic layer by extraction proton transfer reaction the on enables the removal of of th H-C < O <3 H-CI pan 3 and pat C of the i. || | Peter7. Reaction Scheme. о А N 1. xs Mel, xs K2CO3 2. Ag2O, H₂O 3. heat NH2 NH2 or two differnet methods (no same steps/reagents) C5H12N2 Br2, xs NaOH, xs H₂O OHC 1.03 2. DMS CHONBS heat Draw the molecule(s) on the canvas by choosing buttons from the Tools (for bonds and charges), A toolbars. H± 12D EXP. CONT. H C N O S F CI Br Br P F × Incorrect; Try Again; 2 attempts remaining Note that, in the second propagation step, bromine is attacked by the least sterically hindered carbon ra Δ A. Submit Previous Answers Request Answer
- 6) What is the nucleophilic site in the following compounds? H3C-0-CH3 H2C=CH2 CH;NH2 II II A) | = Hydrogen; I| = TT electrons in bond; III = nitrogen. %3D B) | = Oxygen; II = carbon; III = nitrogen. C) Hydrogen; II = carbon; III = carbon. %3D D) | = Oxygen; II = TT electrons in bond; III = nitrogen.Paper-1_(Code-A) 2020 23. Baeyer Villager reactions are among the most useful of all rearrangement reaction. Observe the following reaction mechanism and select the correct statement(s). :OH :OH LOCOCF, OR To Go OCOCF, R CF.CO.H R By migration of Ph: By migration of R: R [A] [B] A) If R = Me, yield (%) for [A] is maximum & major product [A] is formed (B) If R = t - Bu, yield (%) for [A] is maximum & major product [A] is formed (C) IFR = Me, yield (%) for [B] is maximum & major product [B] is formed DIf R = t- Bu, yield (%) for [B] is maximum & major product [B] is formedugen.wileyplus.com/edugen/student/ aintr.uni Klein, Organic Chemistry, 3e actice Assignment Gradebook ORION Downloadable eTextbook gnment Give the major organic product of the following reaction. :O + HN (CH3)2CHI H30+ ? heat OH y.
- Q.2) A.) Write down what the products a, b, c, D, e, F, G, H, i, J and K are in the following reactions. LDA CH;-I 0°C + SOCI; NH,CH,CH,NH, Ag0. NAOH HO. A H,0 LIAIH, H;0 CH,CHCN H Eter Raney Ni HSCH,CH,SH B.) Write down the reduction reaction of each molecule using appropriate reagents, sorting the compounds given below according to their ease of reduction. CH3 но CH CH,0 -CHs C.) Obtain oxidation reduction products in four different ways using benzaldehyde and appropriate reagents and reactions.a) Complete the following reactions: (i) H3C-C-Ci + H2O A + B (ii) HO H;C. CH3 SOCI, с + D + so, (iii) H;O* HCN E F CH;CH, `CH;3 (iv) CH;CH,CH,CH,CH,Br + NH3 G + H excess2 e yllabus Hours YouTube www.cengage.co... What is the most likely major product of the reaction shown? CI # 23 O II OIV 01 OH I O I and IV 4 HCI Search | FanFiction Q French 11 Quizlet C/ II % šô 6 5 ∞ IV CI MacBook Pro CI & 7 * 8 Microsoft Office H... ( 9