32. Option D, Compounds A and D. Example for SN1 reaction, hence racemic mixture formed.
33 . Example for sn2 reaction, hence inversion of configuration occured.
32. Which of the following substitution products will form in the reaction below? 1.0H MOHD меон...
Please explain answer 32. Which of the following substitution products will form in the reaction below? OcH Меон но All of the above. а. d. A & D b. A & B C & B е. с. D
Show the mechanism and provide the product for the reaction below. Short Answer 33. Show the mechanism and provide the product for the reaction below: Br NaCN acetone
thank you so much! 32. Which of the following substitution products will form in the reaction below? 1ОН MeOH Но ? -O d. e. A&D C&B a. b. c. All of the above. A&B D
thank you so much! 33. Show the mechanism and provide the product for the reaction below: Br NaCN acetone
2. For each of the chemical substitution reactions below identify the major products and whether the reaction is likely an SNI or SN2. Br NaCN ethanol-water CH,OH /H,0 Nal (1 equiv) acetone CH,CH,OH 25°C 3. For each of the following compounds provide appropriate reactants and solvent systems to synthesize them by a substitution reaction. Show which type of substitution: Syl or SN2. SH
8) Th e substitution reaction below Time spent: does not work. Provide an explanation of what might be the problem. BrH Br: HO: 9) What could be changed above to allow the reaction to proceed to the 1-bromopropane product? Recall from lab that alcohols can be dehydrated to form alkenes by heating with a strong acid. This reaction follows an E1 mechanism (P, H, and Eg). Dehydration of alcohols H2SO4 heat Alcohol Alkene 10) Why is acid required for the...
1. Determine the mechanism of each nucleophilic substitution reaction and explain why? Draw the products including the stereochemistry. (6 points) Br + CN acetone d. ~ + CH,CO2H - Y Y + POCHE UCH DMSO + TOCH.CH DMF b. + B + OCH + CH4OH DMSO – w ! ho + OCHCH , CH,CH,OH DM . Br + CH3OH + CH3CH,OH
Provide the two products expected and detailed mechanism for the substitution reaction given below. Therefore, show how each product was formed.
Organic chem please help 3. Each of the following reactions gives a substitution product. Identify the major product in each case and indicate whether the reaction is likely to proceed via a bimolecular (SN2) or a unimolecular (SN1) mechanism. (8 pts) SO2CF3 Nal a) acetone CH3OH b) OMs 80% H2O CH3CH2OH c) Br NaCN DMF d)
For each of the following transformations: a) Show all Products formed State whether the mechanism favors SN1 or SN2 b) c) Show stereochemistry (*R/S) where applicable. d) Show an arrow that indicates which side of the reaction is favored, products or reactants. Br acetone + NaCN CH3CH2CH2NH2 ш HСІ он