Question 19 Predict the FINAL (?) product (or a mixture of products) for the following synthetic transformation: A OA ов BCD two enantiomers 1) PhMgCl 2) H₂O 1) NaNH2 (excess) 2) H₂O H2SO4, H₂O HgSO4 1) n-BuLi 2) Br 16 B 1.03 2. Me₂S ? H₂ Lindlar's catalyst D
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- What is(are) the major final product(s) formed during the following sequence of reactions? 01 11 V 1.0₂ 2. (CH₂)₂S C₂H₂O 2 identical molecules ||| =PPhy < IV орнаCan you please answer questions d-j please!Which series of reactions would carry out the following transformation? OTS ? ► View Available Hint(s) NH₂ O 1. NH3 2. NaBH4 O 1. Phthalimide, KOH, H₂O 2. NH₂NH₂, heat O 1. NaN3 2. LIAIH4 3. H₂O O 1. NaCN 2. H₂, Pd
- a) b) c) d) e) 1) BH3/THF 2) H₂O2 NaOH (aq) cold Cl₂, H₂O HBr CH3CH₂OOCH₂CH3 1. Hg(OAc)2, H₂O 2. NaBH4 o 1) 03 (-78 °C) 2) (CH3)S H₂ Lindlar catalystDraw the organic products of the following reactionof 55 > $ 4 Macmillan Learning 101 LL Organic Chemistry Maxwell a) Use three curved arrows to show the elimination of the first hydrogen bromide. Select Draw Templates More presented by Macmillan Learning Complete the curved arrow mechanism of the following double elimination reaction when 2,3-dibromopentane is treated with two equivalents of sodium amide and heated in mineral oil. 15 % / ||| ||| Q Search ***** 5 G : NH₂ f6 6 C H H : Br : Y H Br N ** : Br: & 7 N lipi fg U Erase * 8 N 19 M 144 K Resources b) Use three curved arrows to show the elimination of the second hydrogen bromide. Select Draw Templates lates f10 |||||| C H : NH3 ► 11 Lx Give Up? : Br : More H P Br N : Br: ** : NH₂ F12 ** + Hint Erase BANG & OLUFSEN insert ] р b
- Determine the major organic product for the reaction scheme shown. Br 1.2 Li, Et₂0 2. -C=CH 3. CH3(CH₂)2CI Select Draw / / || G Rings C H More Erase Q2 QSAT a OSG6 + a bio X GP m.ecollege.com/course.html?courseld3D16785381&OpenVellumHMAC=7ff12f8acf82e26893816a5833de5626#10001 O * 引S I Review | Constants Periodic Table Part A Draw a mechanism for the following reaction: H3C CI CH3 HCI Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges where needed. Electron-flow arrows should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be created. > View Available Hint(s) H pxe coNT 6 e EXP. CO P Pearson Copyright O 2021 Pearson Education Inc. All rights reserved. Terms of Use Privacy Policy Permissions Contact Us | nistry.com/myct/itemView?assignmentProblem. 8:27 PM 73°F ^ 10/3/2021 Co search 23 DELL ...Question 27 of 30 > O Macmillan Learning Organic Chemistry Loudon | Parise SEVENTH EDITION Given the biaryl product, select the two reactants that would give this product via a Suzuki coupling. reactants Select two reactants. Pd(PPH3)4 heat, Na₂CO3 ·C=CH Br H H Br MgBr presented by Macmillan Learning