3) Complete the following: Stereochemistry, enantio-, and regioselectivity are important. NO2 NH2 b) d) H3CO f) HO HO type type NBS, hn CCl4 type type Ac₂O, BF3 g) type OH type F Br Benzylic Bromination Hydrogenolysis NHMe + para SO₂CI O₂N NO₂ Ο Ν NO2 type type CO₂ H2SO4/H2O j) CF3 type electrophilic addition, hydration N type
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Please help with part E, F, G:
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- Complete the following: Stereochemistry, enantio-, and regioselectivity are important. CrO3, H2SO4 a) OH Bromination of an alcohol (Sn2) type EtO₂C CO₂Et b) b) d) H3CO type NH2 a) b) H3CO type a) b) OH g) type CN CI h) acetone Swern Oxidation type type CO₂H type Доно i) Me3SICI, Imidazole OSiMe3 Et3N, CH2Cl2 Br type a) Mg°, THF Br j) b); H3O+ H2SO4 (H+) MeOH OMe type typeWhat 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) bromide- Stereochemistry & regiochemistry + T -CEN
- Name the following compound including stereochemistry i CI Br,A 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…Give the major organic product(s) of the following. Include stereochemistry when applicable. 1) Nal Br a) 2) NaCN, acetone 1) NaOC(CH3)3, heat d Br 2) BH₂ THF; 3) H,O,, NaOH(aq) b) c) d) c) 2) KOC(CH3)3, heat Copyright University of California Merced 2022 Br 1) NaOH, heat 2) MCPBA 1) KOC(CH3)3, heat 2) H3O+
- Draw the organic product of the following reaction. CH3 m-CICgH,CO;H • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If the reaction produces a racemic mixture, just draw one stereoisomer. • If more than one product is possible, only draw the major product. opy asteThe AH° values of each compound is given below as kJ/mol. Calculate the entaphy change (AH) value of the following reacti on? 2CaOg) + 2SO2 (g + Ozg) →2 CasO41) -635.5 -296.9 0.0 -1432.7 (kJ/mol) A) 500.3 kJ B) -500.3 kJ С) -1000.6 kJ D) 2365.1 kJ E) -1094.1 kJH H ČH3 Br р. + CH;C=C: in acetone Reaction Type(s) Mechanism(s) Product(s). Stereochemistry (if applicable) q. p-chloronitrobenzene + sodium ethoxide Reaction Type(s) Mechanism(s) Product(s). Stereochemistry (if applicable)
- 5) What is the type of the following reaction: CO,.Et hv Co,E E10,C [6T - 2m) Cyclonddition Cycloaddition [2T + 21] Cycloaddition [4 - 47) - [417- 2m) CycloadditionDescribe the E/Z stereochemistry for the molecules shown below: A: Z; B: Z A: Z; B: E A: E; B: E A: E; B: Z(i) MgBr ? H (ii) H3O* O (R) O Meso O (S) O racemic O Achiral