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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 parta.) b.) LOCH 3 CHO Determine and draw the product of the following reactions. HNO3 / H₂SO4 HNO3 / H₂SO4 c.) ОНС d.) CH3 OCH3 CH3 OCH3 HNO3 / H₂SO4 HNO3/H₂SO4Draw 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
- . Base . The imol 1. The forme e. Bas perfo In 1 Orav cta 1. Steric hindrance is the unfavorable electron-electron repulsion that results when bonds are forced too close to each other. a. Draw the SN2 mechanism using curved arrows for the reaction of bromoethane with Nu:-. siz b. Draw the SN2 mechanism using curved arrows for the reaction of 2-bromopropane with Nu:. vtisizvod c. Given that steric hindrance is unfavorable, predict whether the SN2 reaction of bromoethane or 2- bromopropane would be faster. d. Determine in general the order of reactivity of all alkyl halides in an SN2 reaction (methyl, 1º, etc.)4. det erMIne ane producu uns show Stepwise mechanismwrite mechanism ? CN O H 1. HO. OH H+ (1 equiv.) 2. a) LIAIH4 b) H₂O work-up 3. H+
- a. Draw the dipor b. Here are two different carbonyl bearing molecules. With the knowledge you learned so far explain which one is more stable and why? CH3 H,C H3C b. a.1. Fill in the necessary starting material, reactants or product for the reactions shown below. A. B. C. I. NaNH,, NH, 2. CH₂CH₂CH₂CH₂Cl 1. NaNH,, NH, 2. CH₂CH₂CI 2. Show the complete mechanism for A. and B. from above. Use the back if necessary.Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: OH H,SO, Part 1: A. HSO, for B. H,SO, C. H20 view structure view structure SO2 Part 2 out of 4 OA. H;O" OB. . H,O Oc. Oc. HO draw structure... finish structure OD. H2 報 Next part +.
- b. 1. Propose a detailed stepwise mechanism, using curved arrow notation, for the following. H* LiOH OH a. H H₂O, heat 1. LIAIH4 (xs) 2. H₂O e NH₂ + H H-NⓇ HDraw product F. Select Draw Rings More F. (CHs);P*-CH2¯2. Draw the organic products formed in each reaction. Draw all stereogenic centers using wedges and dashed wedges. a. C. H OH D OH HI (2 equiv) [1] NaH [2] CH3CH₂Br [1] TsCl, pyr [2] NaOCH3 d. e. f. OH HBr [1] NaCN [2] H₂O OH H₂SO4