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- Draw the products of each SN1 reaction and indicate the stereochemistry when necessary. Br + CH;CH2OH b. H20 a.Which of the following reaction conditions would result in Markovnikov addition to an alkene? O[1] BH3; [2] H₂O2/HO™ Cl2 HBr, ROOR CH3OH, H₂SO4Draw the products formed when a-D-gulose is treated with each reagent.a. CH3I, Ag2Ob. CH3OH, HClc. Ac2O, pyridined. The product in (a), then H3O+e. The product in (b), then Ac2O, pyridinef. The product in (d), then C6H5CH2Cl, Ag2O
- t-BUOK -> A is the reacich SN1,SN2 ET or Ez and what is the Br majar product. er EtONa3. Give structure of products A, B and C CH2 - CH₂ -COOH CH2CH2COOH BaCO3 → A NH,-NH, →B. Heat KOH >CWhich reagents Markovnikov orientation? react with 2-methyl-1-hexene in a I. HBr II. H20/H2SO4 II. Br2 IV. ВН3, NaOH, Н2О2, Н2О III and IV II, III, and IV Il and IV O I and II
- Drawthe MAJOR product(s) of the followingreaction. 1) Hg(OAc)2, H2O 2) NABH4 3) Na,Cr207, H2S04, H2O 1. он 1) NaH 2) 8 3) H2O 2. Fuming H,SO4 3. CH;COCI pyridine 4.Draw the products of each SN1 reaction and indicate the stereochemistry of any stereogenic centers. CH3 CH,CO0- H20 H CH3 CBr CH2CH3 a. (CH3)2CH b. CH;CH2Which reaction(s) afford pentylamine in high yield and minimal side products. 1. NaN3 A Br 2. LIAIH4 1. NaCN в Br 2. LIAIH4 1. SOCIl2 соон 2. Excess NH3 3. LIAIH4 1. NaN3 D Br 2. LIAIH4 NH3 E Br 1:1 ratio of reactants
- Draw the products formed when hex-1-yne is treated with below reagent. [1] R2BH; [2] H2O2, HO−Draw the products formed when (CH3)2C=CH2 is treated with each reagent. a.HBr b. H2O, H2SO4 c. CH3CH2OH, H2SO4 d. Cl2 e.Br2, H2O f.NBS (aqueous DMSO) g.[1] BH3; [2] H2O2, HO−4. What are the products obtained from the following elimination reaction? Indicate the major product. CH;CH2CCH3 H2O CI 5. a) Determine the major product that is formed when the alkyl halide reacts with a hydroxide ion in an elimination reaction. CH;CH,CH,CH,CCH3 Br b) For the major elimination product obtained in 5a), which stereoisomer (cis or trans) is obtained in greater yield? Draw the two isomers and provide the names of the compounds.