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- Give the major products CH₂CO3H CH₂Cl₂, Zn(Cu) HCV/H₂O H₂, Pd/C Br₂/H₂Oreactions and products for C9H8O4 C9H8O4 + O2 --> C9H8O4 + H2O --> C9H8O4 + HCl --> C9H8O4 + OH- --> C9H8O4 + Na --> C9H8O4 + F -->TLNEVE-++ACOD n t t G 80. n Tuu 30 BRE 40 20 Oc C d 4000 a b 3600 (a) CH-CH₂-CH₂-CH₂-C=CH (B) CH-CH2-CH2-CH2-CH2-CI (c) CH-CH₂-CH₂-CH₂-CH-CH₂ (d) CH,CH2-CH2-CH2-CH2-CH3 2000 2600 Wa venumberc 2000 1600 1000 600
- PPh3, DIAD CH20H (A) THF mitsunobu H2N sreaction NH2 excess AGOH () (Ci3H20 INS) me I N-me me1) Classify the following dienes and polyenes as isolated, conjugated, cumulated or some combination of these classifications. a) (db) wold mwe eing o niolionsih odt to d ot slon d) 1,3,5-cyclohexatriene (benzene) c) 1,3,6-cyclooctatriene(4) d F3C H (5) + CH3OH Harin HO. (6) OH Br₂C+0 cyclizes -OCH3 CH3OH - H₂O HCI catalyst
- draw the following: CH₂=CH-C=CH₂ Br Br F CH3 FeCl₂/DMSO. C₂H₂/DME/KOH CH3A app.101edu.co Draw the skeletal (line-bond) structure of (R)-1-ethyl-3- ethynylcyclohex-1-ene. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. CH3 H2 C H2 H2 Select to Edit CH Version: 1.0.80 + productionComplete 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 type
- structures for c and d with stereochemistry MeO OMe O OH CH3C(OME)3 heat C p-TSAWhich of the following is/ are alkene(s)? (1) (2) CH;CH=CH2 (3) CH2 = CH-CH = CH2 CH3-C-CH3 A. (1) only (2) only С. В. (2) and (3) only (1), (2) and (3) D.Question 5 (12] 5.1 Provide the line structures of the products K to P in the reactions below. Stereochemistry is required for product L. (7) OH H,SO, Pd/C K 7. Major product only Only one stereoisomer Stereochemstry required NABH, MEOH HCI ZnCl, M NH O.