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Determine the major organic product for the following reaction scheme: 1. 2Li, Et,O CH2 CH,CH, C CH 2. CH НзС— сі Нас (сн), сн(сн), с CH3 CI 2/ 2 3 CH2 2 Нас

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The major organic product will be the alkyl bromide formed by substitution of a tertiary hydrogen with a bromine. CH3 CH3 Br2 light CH(CH3)2 C(CH3)2 Tertiary hydrogen Br 1-Isopropyl-1methylcyclopentane (c) 1-(1-Bromo-1-methylethyl)1-methylcyclopentane As in part (b), bromination results in substitution of a tertiary hydrogen.

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7.2 Reactions and stereochemistry 1. Draw the stereochemical formula for the major organic product(s) in the following reactions by completing the Fisher projections. Me OH H 1. OsO4 2. NaHSO3 Ph Me Ph Me Br2 / H2O Ph 2. Have the following reactions proceeded with syn- or anti- stereochemistry? A A B a. cis-2-butene Me H B H Me Me Me D b. C D ...

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Two novel methyltin complex of kryptofix5 have been synthesized. Me2SnCl2(Kry) compound was prepared by dissolving both metal and ligand in ethanol and dropwise addition of kryptofix5 to dimethyltin dichloride. The reaction mixture was stirred 12 h and product as a precipitate isolated. Melting range of the complex was 173±2˚C. View Notes - Quiz 2 answers - Orgo II from CHEM 262 at University of North Carolina. Quiz 2 Question 1-4, 1pt each. 1. What is the major organic product obtained from the following reaction? 1.

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What is the major organic product obtained from the following sequence of from ORGO 307 at Rutgers University

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115) Provide the structure of the major organic product which results in the following reaction. 116) Propose a mechanism with a hydride shift for the solvolysis reaction below. 117) Provide a structure for the major substitution and elimination product of the following reaction.To remove unreacted starting materials, reagents, and the reaction by-products, further aqueous acid and base extractions were applied (Scheme 1). Employing this methodology, the authors prepared a library of 125 (5 V 5 V 5) amides of type 5 in high purity (> 90 % HPLC) and overall yields ranging from 32 to 85 % (30–100 mg).

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