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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 орнаShort Anver Question 11. Povide ONLY the MAJOR NO MECHANISMS for the following reactions-you include the regiochemistry and stochemistry when necessary HEY ROOR ✓ 1)0, 2) DMS 1) H₂0Ac), HO 2) Na 1) R₂BH 2) NaOH, H₂O₂of 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
- 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, Pd2. Draw the products for the following reaction conditions using the starting material provided. 1. CH3LI; 2. H20 of 1. CH3CH2MgBr 2.H20 1.(CH2CH),CuLi 2. H20Determine 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 ...What is the organic product formed in the following sequence of reactions? Br (1) Mg/ether, (2) CO₂ HOCH₂/H* (1) DIBAL-H, toluene, -78°C heat (2) H*(aq) (3) H*(aq) II H III IV de "a H H I ?3. Identify the products (A-G) of each reaction sequence shown below OH 1) HCI 2) KCN E Br NaOCH 3, CH3OH 1) PCC 2) CH3MgCl 3) H3O+ 4) CrO3, H₂SO4, H₂O 1) LDA, THF, -78 °C 2) CH31 A (C7H12O) C (C4H8O) F (C5H₂N) 1) Br₂, H* (cat.) 2) Li₂CO3, LiBr, DMF 1) LDA, THF, -78 °C 2) CH3CH₂CI 1) LDA, THF, -78 °C 2) CH3CH₂Br ¹H NMR: 6 6.7 (t, 1H); 2.4 (t, 2H); 2.3 (q, 2H);| 2.1 (s, 3H); 1.9 (quint., 2H) 13C NMR: 8 198; 144; 142; 36; 33; 27; 23. D B ¹H NMR: 8 2.5 (q, 2H); 2.4 (t, 2H); 1.6 (sextet, 2H); 1.1 (t, 3H); 0.90 (t, 3H) 13C NMR: 8 210; 45; 36; 18; 14; 8. G (C7H13N)Cambridge International AS Level Chemistry ot boe slo plgmes s al snsdismonooli End-of-chapter questions 1 1-bromobutane will undergo reactions when heated, as shown by reactions A and B. ot dwab on s bl auoltse s boaub svsd 20 swoll gab ods-suai la yel snoso sdr ssiganm n2 monl gnivims noiteibar VU luad CH;CH,CH,CH,Br B CH;CH,CH,CH,OH CH;CH,CH=CH, 90u S1s 2O1D Isdh tuo gomia sli ni qu dgid tod a guch pecoue For reactions A and B give the reagents used in each case. b Reaction A was repeated using 1-iodobutane instead of 1-bromobutane. Explain any difference in the rate of reaction observed. p bas- od mon c What type of organic reaction is A? d Show the mechanism for reaction A. e Reaction A was repeated with 2-bromo-2-methylpropane instead of 1-bromobutane. i Name the organic compound formed. elle ii The mechanism of the reaction with 2-bromo-2-methylpropane differs from the mechanism of smitas nosd asd i anol reaction A. Describe how the mechanisms differ. f What type of reaction is…pe12 Part 2 ad Crapter 1 O NWP Assessment Player UI Appli x ui/v2/assessment-player/index.html?launchld3De7f9ff7e-311b-440d-8832-4aeb728ebe50#/question/25 13 WileyPLUS HW Question 26 of 30 - / 1 OH H30* HO Consider the epoxide ring opening reaction shown. Which of the following represents a step in the mechanism, with correctly drawn curved arrows? HO: H2Ö: HO: Sáve for Later Attempts: 0 of 3 used Submit AnswE DELLSEE MORE QUESTIONS
