This proposed alpha-alkylation reaction would not work. Identify what is wrong with it. 1. LiN¹-Pr₂/THF 2. CH3CH₂Br A CH3 B This reaction would require a different solvent. The wrong base was used. There is a problem with the order of addition. D The nucleophile isn't appropriate for this electrophile.
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- 6. Rank order the following substitution reactions by reaction rate (Fastest to Slowest) OHS structure of DMSO A. || > | > | > IV B. II >> III > IV C. IV > II > | > ||II D. II >> IV > III E. None of the above I || III IV ~ en Br ~ Br CH,NH, CH₂OH CH₂SH DMSO CHÍNH, CH₂OH CH₂OH + Product Product Product Productcan you explain how can we determine major and minor product from these reaction elimination-addition? &=&=1561=6, NH₂ majo CH, NH₂ NH₂ &=-&-&-& majo CH3 OCH, CI NINH, NH 3liq. KNH₂ NH309. Br ΚΝΗ, NH CI CH₁ 80 80 OCH, majo NH, NH₂ mino CH3 mino NH₂ NH₂ NH, NH, CI majo CH3 majo NH₂ NH₂Draw the organic product for this reaction. . OH Submit Answer If no reaction occurs, draw the organic starting material. 98 II... / H₂C-R- ? O P-CI OH ChemDoodleⓇ Try Another Version 4 -Sn [1 5 item attempts remaining ?
- What is the rate-determining step in the mechanism of an electrophilic substitution reaction of benzene? Select one: OA. Attachment of the electrophile to benzene ring. OB. Bonding of catalyst to electrophile precursor. O C. Reformation of acid catalyst. OD. Formation of the electrophile. OE. Loss of H+ ion form arenium ion intermediate to reform aromatic ring.Need your help for this: Show the reaction mechanism for the formation of a. RCONH2 from the reaction of RCOOR' with NH3 b. RCOOR" from the reaction of RCOOR' with R"OH in acidic mediumFor the given SN2 reaction, draw the organic and inorganic products of the reaction, and identify the nucleophile, substrate, and leaving group. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Н..... C=N Organic product Inorganic product CI Draw the organic product. Erase Select Draw Rings More |||| с H N Cl Erase Draw the inorganic product. Select Draw Rings More /// с H N Cl
- My Home OWLV2 | Online teaching and lear X G D /ilrn/takeAssignment/takeCovalentActivity.do?locator=assignment-take IReviaw Toples Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone below. You do not have to consider stereochemistry. Draw the enolate ion in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right comer. Separate multiple reactants using the + sign from the drop-down menu. aste [F ChemDoode Submit Anewer Retry Entro Group 8 more group attempts remaining10. Which one of the following is the best nucleophile in a substitution reaction at a primary carbon. A) CH,COŞ в) Ное c) H₂O D) (CH3)3COO OA OB OC DDetermine the mechanism of nucleophilic substitution of each reaction and draw the products, including stereochemistr CH₂CH3 CI Br + CN d. + CH3COOH a. acetone + -OCH3 e. DMF f. b. C. ||||| a ||||| Br H Br CH2CH2CH3 + CH3OH DMSO H CH3 CI Br + OCH₂CH3 + CH3CH₂OH
- 1. .CI HC C: Li HC CH LICI 2. -CH3 OH Aqueous HO-S- -CH3 acetone g = SN1 Nucleophilic substitution Electrophilic a = Proton transfer addition h = SN2 Nucleophilic substitution b = Lewis acid/base e = El Elimination c = Radical chain f= E2 Elimination substitution Identify the mechanism by which each of the reactions above proceeds from the mechanisms listed. Use the letters a - i for your answers. among 1. 2.In Part 1 add the curved arrows to the nucleophilic acyl substitution reaction mechanism. In Part 2, answer the multiple-choice question about the reaction in Part 1. Part 1 See Periodic Table O See Hint :ö: :Br: Add the missing curved arrow notation. 20 F CI Br I Part 2 Which statement is most correct regarding the equilibrium for the above reaction? Choose one: O The equilibrium favors the right (i.e., Kea > 1) because acetate is a better leaving group than bromide. O The equilibrium favors the right (i.e., Keg > 1) because bromide is a better leaving group than acetate. O The equilibrium favors the left (i.e. Keg « 1) because acetate is a better leaving group than bromide. O The equilibrium favors the left (i.e., Keg« 1) because bromide is a better leaving group than acetate.Identify the major product of the reaction of an alkene shown below. ||| 1. Hg(OAc)2, H2O 2. NaBH4, NaOH ....... ОН || IV ОН о, ОН