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- Question 2 10.2 Predict the product. Br Br ey of (a) (b) O O a P e (d) Br Br Br (e) (c)2 Write the IUPAC name for each compound. Ο COC-M (a) HV Ο 0 || (d) H₂N- C (b) CH₂(CH₂),COCH, OTT HO noitos2) alodo d diw sobirbydaA to noilo ono evig of alcools dikw 39891 abitbydA (8.81 (c) CH₂(CH₂)4CNHCH, no bae totes me to slom 0 O CNH₂ با нио но но но HOOH + HOOO HO HOOOH OHO.HOOD HO || (e) CH₂CO-A iw sobixbydnA to noltoso. driw do A (D681 moitoo@) aoniMA "I w bn shomme a onions to solomeowths of elom ono bas shima Joubo aviy oj vig OH OHO bertiup bios biydisororesidenten (f) CH3CHCH₂COCH₂CH30): 8.22 Predict the product of the following reaction (red = 1. NABH4 2. Нао ? 3. Na 4. CHзCH2Br
- What are the products of the following reaction? (there are two) 1) O3 2) DMS А. В. С. D. Е. F. H. A F C E DChoose an IUPAC name for the structure in 13-d O a. cis-3-propylcyclohexanecarbaldehyde O b. trans-3-propylcyclohexanecarbaldehyde O c. trans-3-Isopropylcyclohexanecarbaldehyde O d. trans-3-Isopropylcyclohexanal e. trans-3-propylcyclohexanal Choose an IUPAC name for the structure in 13-e O a. 2-Cycloheptenone b. 2-Cyclohexenone O c. 2-Cyclopentenone d. 2-Cyclohexanone O e. 3-Cyclohexenone Choose an IUPAC name for the structure in 13-f a. (R)-3-bromo-3-methyl-1-pentene Ob. (R)-3-bromo-3-methyl-2-hexene С. (S)-3-bromo-3-methyl-1-hexene d. (R)-3-bromo-3-methyl-1-hexene e. (R)-3-bromo-3-methyl-1-heptene12. (10 pts) Under the right conditions radical bromination of A produces compound B as shown below (this is termed allylic bromination): hv Br Br2 A B Write a detailed mechanism for the propagation steps of the above radical bromination, showing how the products are formed and that the radical used in the first step is formed in the last step (use curved arrows to show electron flow).
- The increasing order of reactivity of HX towards ether is: (A HI,HBr,HCI B HCI,HBr,HI HCI, HBr, HI HI, HCI, HBr10. E to CH3ONa a) Br₂ Br2 1. Mg /ether khan (A) (B) (C) (D) hv FeBr3 hv 2. CO2 3. H3O+ C1 B2 B3 B1 KMnO4 H+ C1 Mg, ether CHO b) 1. CH3Mgl H2SO4 HBr 1. Mgether khan A B D to 2. H3O+ peroxide 2. H₂C-CH2 ° CH3COCI AICI 3 1. C1 1. 03 G F E 2. H3O+ 2. Na₂S 3. H3O+Options for left to right: a) Fe/HCl b) Br2/FeBr3 c) NaBH4/H2O d) HNO3/cat. H2SO4 e) H2O/HCl Options for top to bottom: a) Fe/HCl b) Br2/FeBr3 c) LiAlH4/H2O d) HNO3/cat. H2SO4 e) PBR/DMF Options right to left: a) HNO3/cat. H2SO4 b) NaNO2/cat. H2SO4 c) Fe/HCl d) Br2/FeBr3 e) NaBH4/H2O