The following conversion involves sequential Heck reactions. Propose structural formu- las for the palladium-containing intermediates involved in this reaction. Heck reaction ELOOC. ELOOC. SiMeg ELOOC ELOOC SiMeg
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- 7. 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 CHOProvide the products and detailed arrow pushing mechanisms for the following reactions: OSIME3 EtN CO.Me 1. base, dilute solution (10mM) 2. NaOH/MEOH-H,0 Acid, heat CO.Memheducation.com/ext/map/index.html?_con=con&external_browser=D0&launchUrl=https%253A%252F%252Fcompass2g.illinois.edu%252Fweb wing i Saved Complete the reactions to show the synthesis of the following compound from (CH,),CHCH,CH,Br. Part 1: Br K OC(CH3)3 view structure Part 2 out of 2 Br2 H,O What reagent is needed where the "?" is located?For each of the reactions pictured A) Give the Woodward-Hofmann classification. B) Use a frontier molecular orbital analysis to tell whether the reaction is an allowed thermal or photochemical concerted reaction. Ph. .. Ph a) Ph Ph CN CN CN b) CN H,CO,C Co,CH3 c) H3CO2C Co,CH3 H. d) CH3 H3C. CH2OSI(CH3)3 Os((CH3)3 H3C H,CH3C HPrediga los productos de las siguientes reacciones. (a) éter sec-butil isopropflico + HBr conc., calor (c) éter di-n-butflico + NaOH conc. caliente (e) etoxibence no + HI conc., calor (b) 2-etoxi-2-metilpentano + HBr conc., calor (d) éter di-n-butllico + Na metálico (1,2-epoxihexano+H*,CH,OH6. Complete reaction scheme below indicating reagents, catalysts and conditions, and side product trigil bezinslog si6101fon 290b 1l (b Senines levirba 6 gaubong nasamots gniwollot ads to doinW 01 sniowl (6 CH3 40 CH3 Scansgowi (d Ege nodie) ( nsgyxo (b NO₂ 19m02 2i gniwollet sits to mainW II HOWrite the reaction flow chart fir the following condensation and further heating of resulting productsPredict the products by showing the reaction mechanism (arrow pushing) of the given diagram.1. MCPBA; H3O+ 2. OsO4, Na2SO3/H2O 3. H3O+A. Select the expecked Mojor pruduct of the reactiun Shawn く Sekct the expected product of the following reachon NacN DMso Which Compound would be the product of the realhm ヘMgbr 3. PCC 4. H2 N N Hz01:50 4G File Details 4CH003/UM1: Fundamentals of... Introduction NaBH4 OH C=0 H benzophenone diphenylmethanol Ketones are readily reduced to secondary alcohols by reaction with sodium borohydride. The aim of this experiment is to determine the time required to effect the complete conversion of the ketone, benzophenone to diphenylmethanol at room temperature. This investigation may be achieved by isolating and analyzing the reaction product after different reduction times. Infrared spectroscopy affords a convenient method of analysis; by comparing the IR spectrum of the crude reaction product at different time intervals one would expect to see the intensity of the hydroxyl absorption peak increase relative to that of the original carbonyl peak. From this you can deduce the optimum time for the reduction process at room temperature. Procedure Note the "reduction time" that the demonstrator assigns to your group. Different groups will be assigned different times, eithert = 2.5 minutes,…Which of the following reactions is /are feasible? NANH2 NaCI H3C CI NH3 H3C NH2 II SOCI2 OH H3C OH H3C CI IV II O lonly O , II and IV O T and Il only I and IV only11. BONUS Question: Predict the product for the following reaction. `NH2 , H2SO4_ HN но II IV А. В. С. D. Е. -==>>SEE MORE QUESTIONS