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Q: the dehydrohalogenation (E2) reaction, d
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- What is the name of the following compound +1 Br Brill.. |||| OH₂ OH₂ Co Br H₂O OH₂ trans-teraaquadibromocobalt(1) bromide trans-teraaquadibromocobaltate(1) bromide Ocis-teraaquadibromocobalt(1) bromide cis-teraaquadibromocobaltate(1) bromide2. Fill in the major product of the following reactions. Include stereochemistry when appropriate. all ebuloni abnucqmoo privolial arts to atinja intel -omoid-S-(3) ensilexeromond-4-(S) on KOtBu tBuOH ya CI KOtBu tBuOH CI NaOMe MeOH NaOMe MeOH EtOH CI MeOH benogoto to is heat congid of evol mon aheat malwollot erti (teawol ediIdentify the major product of the reaction of an alkene shown below. ||| 1. Hg(OAc)2, H2O 2. NaBH4, NaOH ....... ОН || IV ОН о, ОН
- Proufde the product of the FOlLourng or reacton sequences. Aease draw the apropriate Stereoehemistry In Cases ohere you expecta racemate please prouide BO TH enantiomers. In where you excpect aperoximately equal amourts of eliastereomers, please oliastereomess. reachons cases prouide all OEt A. Breleauivalent). Ethanol /Na DEt CongD HCL Benzoyl peroxide C.What reagents are appropriate to carry out the conversion shown? - OH LOM 1. mCPBA; 2. CH3MgBr; 3. H₂O O 1. CH3MgBr; 2. H₂O O 1. mCPBA; 2. H₂O O mCPBA + enantiomerA eFundi : Home : Overview E NCHE 121 - Module test - Versio X G Which one of the alkenes can for x b My Questions | bartleby + A https://docs.google.com/forms/d/e/1FAlpQLSeaeyD2qYYYa712LcEehfMLha7DEaTq1KXQ5g7o2byUrT8CnA/formResponse Question 4: The alkene 2-methylbut-2-ene reacts with hydrogen cyanide (HCN) to form the Markovnikov product. Write the preferred IUPAC name of the main product of this reaction. [Use lowercase letters. Do not use spaces if it is not required in the name.] * Your answer Question 5: Which statement about electrophilic addition reactions is not true? * Markovnikov's rule explains why the addition reactions of unsymmetrically substituted alkenes are regiospecific. Markovnikov's rule does not apply to internal alkynes. The larger amount of the nucleophile will bond to the more stable carbocation during an electrophilic addition reaction. None of these statements are correct. O All of these statements are correct. Question 6: The mechanism in Figure 6 produces…
- The triplet excited state of the boxed molecule will react with the ground state of the alkenes shown. Give the major regioisomer for each product in the order A, B, C, and D. and opsin are reassembled me to form Sme CEN I sdono A Trege head-to-head; head-to-tail; head-to-tail; head-to-head head-to-tail; head-to-tail; head-to-tail; head-to-tail head-to-head; head-to-tail; head-to-tail; head-to-tail 11-cis-retinal head-to-tail; head-to-head; head-to-tail; head-to-headWhich of the following represents allylic carbocation? CH, - CH = CH, CH3 - CH = C - CH3 CH3 - CH- CH = CH2 II III 1 & III -b & ||COExplainwhythefollowingdeuterated1-bromo-2-methylcyclohexaneundergoes dehydrohalogenation by the E2 mechanism, to give only the indicated product. Two other alkenes are not observed.
- This Diels-Alder reaction prodoces a rmcamic producr mixnare. In the box below draw the stracture of one of these stereoisomers. • Lae Ibe wodgerhash beod tools to indicate stereochemistry where it cxista. • Include Hatoma at chiral centers only. • Ila group is achiral, du not use wedyed or hashed bunds en il:) Predict the NAME, STRUCTURE and STEREOCHEMISTRY of the BEST ORGANIC REACTANT or the MAJOR ORGANIC product for the following reactions: CH2 МСРВА, НзО* meso 3,4-hexane diol FoH H+OH CHCH a) (name, str, stereochem) ? HCI b) 3-methyl 1-pentene - ? (name, str, stereochem) c) methylcyclohexane ----Br2, hv------? (name, str, stereochem) 40H d) ? (name, str., stereochem) Os04, water----meso cyclohexane 1,2-diol ----[Review Topics] [References 1. Cl, HаO 2. NAOH Another mechanism for the formation of epoxides is through the formation of a chlorohydrin. Alkenes react with chlorine in the presence. of H,O to give a chlorohydrin via a cyclic chloronium 1on intermediate. Whem the chlorohydrin is treated with strong base, HCl is eliminated and the epoxide is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions oH2 Retry Entire Group 9 more group attempts remaining Submit Answer 8:44 PM :0: