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- What is the expected major product for the following reaction? O IV I OCH 3 |||||... + enantiomer || 1. Hg(OAc)2, CH3OH 2. NaBH4 НО. OH ... H3CO. + enantiomer ||| IV H3CO VCyclohexene plus 1) Hg(OAc)2, H2O; 2) NaBH4; yields __________. HO2CCH2CH2CH2CH2CO2H a cyclic diketone cyclohexyne cyclohexanol OHCCH2CH2CH2CH2CHOf4 4 Macmillan Learning 101 F LLI Draw the major organic product of the reaction. Show the stereochemistry, if applicable. Omit byproducts such as water or bromide ion. % Q Search 5 G f6 6 Br Y & H HO™ 7 lip fg U * + 00 Select / ||| ||| S G N fg Σ Draw Templates 9 Templates More K C JO f10 H 0 ► 11 112 CH 2 Q 0 + Erase BANG & OLUFSEN insert pr ba
- Which of the following reactions will produce acetophenone as a major product? OH CI AICI 3 OL Ör = ооо == ||| IV all of these 1.03 2. DMS || IV PCC CH₂Cl2 H 1. CH3MgBr 2. H₂O 3. PCC/CH₂Cl2Acceptable Mechanison? - Œ 50% a I Acceptable Mechanismy- Ph-= -Pr 10215, CH3CH2NH₂ ZonMy Go (31)Provide the product for the following reaction? НО. 1 || IV HO HO Na₂Cr₂O7, H₂SO4 excess HO
- 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. 2.34. Draw the major organic product(s) for the following reactions; (*) must include correct stereochemistry; double-dagger (+) must show two products. HBr (a)* Br HBr Br (b) + (1.00 equiv.) Br Br HBr (c)* HCI (d) 48% wt. HBr 37% wt. HCI HEAT OH [H2SO]/ H20 (g) OCH3 [H2SO,]/A CH,OH (excess) (h) [H,SO,1/H20 OH (i)* [H2SO,] / H,0 OH 13A 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…
- What is the predicted product of the following reaction? === HO OH I CH3CH2O OCH2CH3 ||| excess CH3CH₂OH H₂SO4 HO OCH₂CH3 || IV OCH₂CH3Determine the major organic product for the reaction scheme shown. Br 1.2 Li, Et₂0 2. -C=CH 3. CH3(CH₂)2CI Select Draw / / || G Rings C H More Erase Q2 Q3 E C Draw the final organic product of the given reaction. 28 $ 4 R F V OH 5 Search or type URL T G CHỊCH,NH, heat B 6 MacBook Pro Y H N H₂O + & U J 8 Select Draw Templates More M / |||||| NO alt ZA 3 - K ( 9 H V- I O C 20 ỏ L N 0 command O 43 P A. H : ; Q2Q option Aa { [ + ? I O Erase 1 delete re