Predict the starting alkyl chloride that would produce the product shown in the SN1 reaction. Assume no rearrangements. Stereochemistry is not considered. Incorrect, 2 attempts remaining Select to View feedback I I 1 I CH3CH₂OH I I I I I X F
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- 3. Draw the complete reaction mechanism in each step for the formation of compound C and D. i) ) PdCl (M CN), 1) -CH(CO,Et); Ph Ph. Ph (EtO,C)HC, N O li) co H- 60 - 95% R 97% de iv) Me,SnR co,Me ÓTMS Pd(OAc)2 CH,CN CO2Et 55%Institution 61 - STOCK YARDS BA X → CD app.101edu.co # Predict the starting alkyl bromide that would produce the product shown in the SN1 reaction. Assume no rearrangements. Stereochemistry is not considered. Type here to search LG energy w Pedro Merino Farinas - 023065- X Drawing HID H₂O OH https://ew31.ultipro.com/pages/X Question 10 of 32 Atoms, Bonds and Rings H₂N MENU AUTO/SET H HO HS f-ENGINE SOURCE Aktiv Chemistry Br Charges X لا أ GMy 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 remaining
- biackboard.gwu.edu/webapPps/assessment/feview/review.jsprattempld Select the major product of the reaction below. 1) TIPSCI, Et3N 2) Na 3) 03, then CH3SCH3 4) CH3CH2LI, then H30* 5) Bu4N* F', H2O CI Selected Answer: Он HO Answers: он он он OH OH OH он Select the major product of the reaction below. The answer is there, but please explain step by step.can 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 NH₂In each reaction box, place the best reagent and conditions from the list provided. 1) Br 2) 3) DEET (the active ingredient in over the counter insect repellant) 4) 5) Answer Bank Mg. Et,0 CH,CH,OH НСООСH, H,CO НСООН NH(CH,CH,),(2 equiv.) Br,, FeBrz CH,COOH HN(CH,CH,), (1 equiv.) NaNH, H,0+ CH,CH,NH, CO, CH,CH, Br SOC, NaCN
- Acceptable Mechanison? - Œ 50% a I Acceptable Mechanismy- Ph-= -Pr 10215, CH3CH2NH₂ ZonMy Go (31)Mity.dorlocator%=Dassignment-take Not syn [Review Topics] [References] Br 1. +. KOt-Bu KBr HOt-Bu "Br Aqueous acetone H2O H3C HBr Br H OH optically active racemic a = Proton transfer e = Electrophilic addition h = Sy1 Nucleophilic substitution b= Lewis acid/base f= El Elimination i= S2 Nucleophilic substitution %3D c = Radical chain substitution g = E2 Elimination j= Electrophilic aromatic substitution d = Radical chain addition Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -j for your answers. 1. Submit Answer Retry Entire Group 8 more group attempts remaining 2. 2.Show the mechanism for the following Show relevant resonance structures , and label each step (Sn2, protonation .) Use appropriate arrows (equilibrium, resonance,etc). а. HSnBuz AIBN, heat CI Br b. H-/H,0 но C. Meo OMe HCI (catalytic) EIOH Br Br HN Ph Ph d. NH,NH, (excess) MEOH но
- Choose the best sequence of reactions for the transformation given. Semicolons indicate separation steps to be used in the order shown. A) H,O*; SOCl,; SOCI₂; C6H5CO2CH3 || CoH5CH2CNHCH3 CHÍNH, B) HO/H,O; PBrạ; Mg; CO,; H,O*; SOC1,; CH,NH, C) LiAlH; H₂O; HBr; Mg; CO₂; H₂O+; SOCI₂; CH₂NH₂ D) None of these would yield the desired product1. .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.Gve the major product of the following reaction. CH,CH,ONa H. HO. HO. L There is no reaction under these conditions or the cor«.Lproduct.is not fisted here,