The addition of chlorine to the alkene shown will give products that are: CH₂CH3 H C=C H3C H one meso compound two meso compounds a pair of enantiomers O four different stereoisomers
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- Indicate the products of the reaction with their name and stereochemistry: Å CH₂ CH3 C6H5 H₂O, H+Give the Major product(s) and name the starting compound with stereochemistry: H2O H2O H2SO4 H,SO, HgSO,Draw a structural formula for the major organic product of the following reaction: CH2Cl2 Cl2 Show product stereochemistry IF the reactant alkene has both carbons of the double bond within a ring. • Do not show stereochemistry in other cases. • If enantiomers are formed, just draw one. орy вste ChemDoodle
- Indicate the stereochemistry of the product of SN2 reaction: NaOH Br CH3 CH;OH Name the product:What is (are) the major organic product(s) obtained from the following reaction? Br2 O (2R,3R)-dibromobutane meso-2,3-dibromobutane O (2S,3S)-dibromobutane O Racemic mixtureWhat is the stereochemistry of the alkene below? W = FCH2CH2; X = fluoro; Y = bromo; Z = isopropyl W -x OE OZ Oneither Y N
- Draw the structural formula of the product of the reaction shown below. + H₂O AAVIL H₂SO4 • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If the reaction produces a racemic mixture, just draw one stereoisomer. Sn [F Ⓡ ChemDoodle(a) (R)-2-Bromobutane undergoes light-induced reaction with Br2 to yield a mixture of products, among which are 1,2-dibromobutane and 2,2-dibromobutane. Write the reaction showing the correct stereochemistry of the reactant. Which of the two products is optically active? Explain. ENG bj hp 17 fe 19 fho is f6 12 米 $4 4 3. & 7 23 2 8. E T Y 5 96 %24Draw all of the substitution and elimination products formed from the given alkyl halide with each reagent: (a) CH3OH; (b) KOH. Indicate the stereochemistry around the stereogenic centers present in the products, as well as the mechanism by which each product is formed.
- Which of the following reactions of alkenes takes place with syn stereospecificity? O addition of bromine (treatment with Br2) O oxidation (treatment with OsO4) addition of H2 with Pt O Hydroboration Oxidation O B, C and DThe bicyclic alkene P can be prepared by thermal electrocyclic ring closure from cyclodecadiene Q or by photochemical electrocyclic ring closure from cyclodecadiene R. Draw the structures of Q and R, and indicate the stereochemistry of the process by which each reaction occurs.Draw a structural formula for the major organic product of the following reaction: CH2CI2 Br2 CH3CH=CHCH2CH(CH3)2 + Show product stereochemistry IF the reactant alkene has both carbons of the double bond within a ring. • Do not show stereochemistry in other cases. • If enantiomers are formed, just draw one. opy aste - [F ChemDoodle