5. Determine the products for each of the following reactions. Label each carbonyl group as either a ketone or aldehyde. (Note: DMS stands for dimethyl sulfide - CH SCH3) a. 1) O3, -78°C 2) DMS b. 1) O3, -78°C 2) DMS K
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- Please helpcomplete the reaction 68Draw the product of the given reaction between a ketone and an alcohol. Select Draw Rings More Erase // H. C H* + 1 mole equiv. HO-CH2-CH3 .C. H3C CH3 How would the product of the reaction be classified? O It is an acetal. It is an alcohol. It is a hemiacetal. It is a ketone.
- 5. Which of the following reagents would transform the reactant into this product? CI a. 1) OsO4 2) H₂O₂ b. 1) MCPBA 2) NaOCH, 3) dilute acid c. 1) MCPBA 2) H₂OCH3 /HOCH₁ d. 1) BH3 2) H₂O₂/NaOH/H₂O CI- OH C1. Draw the product formed when the following ketone reduces with NaBH4 in CH3OH. DIBAL-H (H3C)3C- (H3C)3C- A. I OH охон B. II OCH 3 C. II and III CH3OH (H3C)3C D. IV || -COOH E III -OH IV -OHSynthesize the following compound from cyclohexanol, ethanol, and any other needed reagents. 2 Part 1 out of 3 Preparation of the Grignard reagent: ok nt nces A OH draw structure ... draw structure ... Draw the intermediate product formed above and select the correct reagent for A. O MgBr, O HBr O NaBr O Br2 Draw the Grignard reagent formed above and select the correct reagent for B. O Mgo O MgBr O MgI, O Mg Hint Solution e to search K.
- What reagents are needed to carry out the shown multi-step synthesis ? Br Br Br Br O 1. 1.) LDA; 2.) HBr 2. 1.) H9SO4; 2.) NaBr none of the shown reagents will work 3. 1.) NaOH; 2.) HBr 4. 1.) Li; 2.) Br2 O 5.Complete the reactions given belowDraw the structure of the organic product formed when the given compounds undergo the three-step reaction sequence indicated. Select Draw Rings More Erase C Br 1. NaOC,H5. C,H5OH 2. NaOH, H2O 3. H3O*, heat
- Pick all reactants (list is shown in separate picturesIn Part 1 add the curved arrows to the nucleophilic acyl substitution reaction mechanism. In Part 2, answer the multiple-choice question about the reaction in Part 1. Part 1 See Periodic Table O See Hint :ö: :Br: Add the missing curved arrow notation. 20 F CI Br I Part 2 Which statement is most correct regarding the equilibrium for the above reaction? Choose one: O The equilibrium favors the right (i.e., Kea > 1) because acetate is a better leaving group than bromide. O The equilibrium favors the right (i.e., Keg > 1) because bromide is a better leaving group than acetate. O The equilibrium favors the left (i.e. Keg « 1) because acetate is a better leaving group than bromide. O The equilibrium favors the left (i.e., Keg« 1) because bromide is a better leaving group than acetate.027 In Part 1 add the curved arrows to the nucleophilic acyl substitution reaction mechanism. In Part 2, answer the multiple-choice question about the reaction in Part 1. Part 1 4 See Periodic Table O See Hint :0: :Br: Add the missing curved arrow notation. S CI Br Part 2 Which statement is most correct regarding the equilibrium for the above reaction? Choose one: O The equilibrium favors the right (i.e., Kea > 1) because acetate is a better leaving group than bromide. O The equilibrium favors the right (i.e., Kea > 1) because bromide is a better leaving group than acetate. O The equilibrium favors the left (i.e., Keq« 1) because acetate is a better leaving group than bromide. O The equilibrium favors the left (i.e., Keg 1) because bromide is a better leaving group than acetate. +