on 14 of 25 > O₂N NO₂ Stacked Modify the bonds to wedge and dashed bond to show the stereochemistry of the product. Select Draw Templates Groups C H More NO₂ H H NO₂ Erase
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- Draw the structures of organic compounds A and B. Indicate stereochemistry where applicable HTC=C-H 1. NaNH, P 2. CH3CH₂CH₂Br (1 equiv.) Draw compound A. Select Draw Templates More / ||| ||| C H compound A Erase H₂ Lindlar's catalyst compound B Draw compound B. H₂O H3O+ Select Draw Templates More / ||| ||| C H OH Era.(J) H H3C H a CH₂l2' Zn(Cu) Et2₂O CO₂Me b* H* H₂OQ, - write a Mechanism that explains hint he stereochemisty (sed pmacal rearangemendy a) CotH6 fonn Hcl b) HeoH O wr,te he Mechanism fer OH CHBrg NAOH (Carbene)
- Determine 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 + CH3CH₂OHDraw the major prodct from this reaction. Use a dash and/or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Ignore acid byproducts. mCPBA < On Q 000 Atom anc Draw or MacB14) How mony total Can Structures for this intermediate E How sunt el of q Diteitsste Hest so 350 30574x9 DTON of H₂CO. resonance be draun rt econte 30. brip pupa yon al em 3m papio to cane Shon nostrog9079 senioro To
- 2. 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 ediGive the major products for the reaction. Cl₂ (low conc.) Select Draw Templates More / |||||| S C cl H T Erased) Explain why product C is racemic but product D is non-racemic. Br CH,OH fonnet Siz mechinmwhin mes in inversion of the procdnct odue to Hhen bukside ata from the Mactoprile Br NaSH D
- Which statement is correct for the following substitution reaction? of acetone + NaSH Br Select one: O the product is optically active O it is a unimolecular reaction O it is faster in aprotic solvents O the rate is unaffected by changing the concentration of NASH Oit gives a racemic mixtureUse the References to access important values if needed for this question. Draw the structure of the product that is expected when the following compound is treated with concentrated H2SO4. он H2S04 ? heat CH3 You do not have to consider stereochemistry. • In cases where there is more than one answer, just draw one. ited opy Bste [F CH4 ChemDoodle Retry Entire Group 3 more group attempts remaining Submit Answer Previous Next Email Instructor Save and Exit Cengage Learning | Cengage Technical SupportDraw the remaining product of the given reaction. of CI + H₂C-O- Select Draw Templates More / |||||| C O H CI Q2Q Erase +C
