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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 орнаWhich 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, PdShort 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, H₂O₂
- 2. 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 Q3. 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)SAT 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 ...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…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 ?What is the major organic product of the following reaction? а) CH3CO2NA -C-CI b) 1. НО ОН 2. CH3MGB. 3. Hзо*, д c) 1. NaCN CH3-CH2–CH2-Br 2. H30*, ASEE MORE QUESTIONS