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- Draw a stepwise mechanism for the following reaction: H,SO Part 1: A. HSO, or B. . H,SO, +. OC. H20 view structure D. SO, view structure Part 2: OA. H,0 В. Н.О C. HO view structure OD. H2 view structure Part 3 out of 4 edit structure ... edit structure ... Gr Next partOraw a stepwise mechanism for the following reaction: Br CH3CH2OH Part 1 out of 3 HBr Br Br CH3CH,Br finish structure ... draw structure CH;BrDraw a stepwise mechanism for the following reaction: Br CH3CH2OH Part 1 out of 3 HBr Br i Br CH;CH,Br finish structure . draw structure ... CH3B Next part
- 1. Draw the products of each nucleophilic substitution reaction a. b. D b OH C. d. e. f. Br 1 NaCN + NaOCH3 H₂OSynthesize each compound from cyclohexanol using any other organic or inorganic compounds. CH,OH a. g. (Each cyclohexane ring must come from cyclohexanol.) COOH b. d. h. сно CHs (Each cyclohexane ring must come from cyclohexanol.)Draw a stepwise mechanism for the following reaction: H,SO 4 Part 1 out of 4 OA. HSO4 OB. H,SO4 HOH В. OC. H20 finish structure ... draw structure ... OD. SO, Next part
- 1. Name the starting compound and then draw a reaction. stepwise mechanism for the following Cl2 .Cl H2ODraw the following compounds: 2-methoxypentane a. b. (E)-3-chlorohex-2-ene constrate aa. b. C. d. e. type: OH type: type: OH 2 + OH TsOH cat. HÅH н Ἡ Acetal formation OH TsOH cat. SOCI₂ ܘ ܀ 1.2 equiv. NH3 2. LIAIH₂ 3. H₂O*
- 48. Which set of reagents would accomplish this conversion H. H. CH3OH with H* as a catalyst NaH followed by CH3OH CH3ONA followed CH3OH CH3ONA followed by CH3Br a. b. C. d.O#1 Draw all possible constitutional isomers formed by DEHYDROHALOGENATION of each alkyl halide. Br CI Br b. а. С. d.Give the IUPAC name for each aldehyde. CH, CH;CHCH-C-H a. CH;CH;CH;-C-CH;CHs сно b. c. (CH):CHCH:CH:CHO d. (CH:).CC(CH):CH:CHO Cire the IUPAC ваше for each ketone/ CH3-C- CHCH2CH3 CH2CH3 ČH3 ČH3