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- Which sequence of steps will give the highest yield of a carboxylic ester product? Mix 0.1 mole of benzoic acid (C6H5CO2H) with 1.0 mol SOC12, remove unreacted SOC12, then add 0.1 mole of isopropyl alcohol O Mix 0.1 mole of benzoic acid (C6H5CO2H) with 0.1 mol of NaOH, then add 1.0 mol of isopropyl alcohol and heat, Men remove any unreacted isopropyl alcohol O Mix 0.1 mole of benzoic acid (C6H5CO2H) with 0.1 mol of NaOH, then add 0.1 mol of isopropyl alcohol and heat Mix 0.1 mole of methyl benzoate (C6H5-(C=0)-OCH3) with 0.1 mol of isopropyl alcohol and stir overnightComplete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible answer. 1) CH3CH2M9B CH3OH H+ (ехcess) но 2) H30*, H2O B A OCH3Identify the products of hydrolysis of a triester shown below (the products that form when a compound shown below reacts with water in the presence of an acid). H,C-O-C-(CH)15CH3 HC-C O- (CH)12CH3 H2C-O (CH-) 1CH3 ype here to search Prise F10 F11 F5 F6 F7 F8 F9 F2 F3 F4 & 4 5 6 E R T Y. * CO
- Which is the major product from the acid catalyzed hydrolysis of cyclohexene oxide? но OH но он || II IV1. Each of the nucleophilic substitution reactions shown below are reported in the chemistry literature. Predict the expected product of each reaction Br Me. Br OH NaOCH₂CH₂ONa DMSO CI OTS NaOH H₂O NaN3 DMFProvide a mechanism that accounts for the outcome of the following hydrolysis reaction. H3O+ ?
- C15T09Q9684 Give the major product of the following reaction. NaOH H+ F- -NO, heat O,N HO- O,N N- H OMe F- N. Meo NO2 There is no reaction under these conditions or the correct product is not listed here.Draw the product of the reaction below. Ignore inorganic byproducts. НО I Н. I I но OH OH Ag2O ОН Н excess CH3I -OH g WWhich of the following reactions will NOT work to provide propyl butanoate as a product? + H,SO4 HO. HO H2SO4 `NH2 но Pyridine (base) OH O:
- Give the major product of the following reaction. NO, NaOH H+ O,N- heat NO, O,N NO2 O,N- OMe -N F- N- H There is no reaction under these conditions or the correct answer is not listed here. O,N OMe Meo F OMe NO2 O,N- H. O,N F H.a) Using your knowledge of organic reaction mechanisms, explain the formation of EACH product (A,B) in the following reaction. This will require you to write out MULTIPLE mechanisms (i.e. each product comes from a different reaction pathway). Hint: all reaction pathways start from the same intermediate: NaH is a strong base but cannot deprotonate an sp3 C-H bond! OH он 1) NaH (0.5 equiv) Br + 2) H20 A B b) Briefly explain why there is no epoxide (formed via an intramolecular substitution reaction) in the product mixture of the above reaction?Predict the major product(s) of the following reaction. H₂SO4 OH ??? наю " нохо ""т НО HO