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- envellum.ecollege.com/course.html?courseld%3D16785381&OpenVellumHMAC=D7ff12f8acf82e26893816a5833de5626#310001 SHOmewOrK #4 Problem 12 12 of Propose a mecnanism or ihe following reaction: CH3 CH3 H20 HQ CH3 H* CH3 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 an atom or a bond and should end on an atom, bond, or location where a new should be created. H EXP. . ? CONT. CH CH, +) H. Pearson 8:29 )耳. @ here to search 73°F 23 10/3/ DELLWhich of the following reagents is needed for this reaction? ? ► View Available Hint(s) = O Na+ -NH2 O H2, Pd/Pb(OAc)2 O Naº, NH3(1) O H2, Pd/C ndin Progress E Choose the correct missing reagent/condition for the following reaction. To preview the image click here O H2, Pd/C OH O H2/Lindlar Catalyst O Na/NH3(1) Q Search -inder- $ 4 F "Jo %9 5 amix 24 a hp ㄱ bp
- Problem 3 of 16 Draw the products of this reduction of a ketone with sodium borohydride. 1) NaBH4 49 Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicableIgnore any inorganic byproducts. 2) HCI/H₂O Submit Select to DrawWhich product(s) would form under the conditions given below? byla D 1. 0₂ 2. Me₂S QA OB O C OD O A and B O C and D O A, C, and D Save for Later B с H Submit AnswerOM OM MOM OUG fil app.101edu.co Maps M Gmail YouTube X 20 F3 E D O X G d GWGW Question 27 of 31 What is the major product of the reaction shown below? A) butane B) 1-butene H₂ Pt, heat C) 1-butyne D) 2-butyne E) No reaction occurs. V Aa F4 C $ 4 R F 07 dº % 5 V P F5 T G B > 6 n MacBook Air F6 B Y H H C 2 & 7 F7 N * 00 8 J DII F8 1 M W G1 CS 9 K F9 O O UONEE H L F10 Done P B Gra F11 لا۔ + 11 { ? I command option + F12 11 Update Subm + 1 T
- Problem 11 of 32 Draw the product of the substitution reaction shown below. Ignore the inorganic byproducts. CH3CH₂I DMSO OO (+) Submit Na2) Chap 11 problem a) Give the arrow-pushing mechanism for the following cross-metathesis reaction catalyzed by Grubbs Ru-gen-Il catalyst, which you can represent in your mechanism as [Ru]=CHPH. b) Why is the cross-metathesis product ultimately favored over self-dimerizations? c) Why is the E isomer favored over the Z isomer? `N' CI| RuPh Ru-Gen-I| PCY3 Ru-Gen-Il (2 mol%) CH,Cl2, 40 °C, 12 h OMe ÓMe (1.5 equiv) 92% yield, only E +find theoretical yield of 102 mg of 4-tert-butylhexane equation is C10H18O please show work. table with info attached
- Qurston 18 Consuder the reatons shown. CI (8) t HCI cl + H2 What type of resction in it? Which is the corred product A,B or C? Name the first reactant the second reactont Name theWhat is/are the reagent(s) for the following reaction? d-d Problem viewing the image. Click Here ↓ O HgSO4, H₂O, H₂SO4 O H₂, Lindlar catalyst O Na, NH3(1) O 1. (Sia)2BH.THF 2. OH, H202 O H₂, Pd/CQuestion 9 of 22 Incorrect. Choose the major product that is expected for the following reaction sequence: 1) NaNH, 2) Mel H-C=C-H O < 3) R₂BH 4) H₂O₂, NaOH LOH LOH eTextbook and Media O Search LDL OF