Predict the major and minor products that would be obtained from each of the following reactions. Give the mechanism (SN1, SN2, E1, or E2) by which each product is formed.
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Predict the major and minor products that would be obtained from each of the following reactions. Give the mechanism (SN1, SN2, E1, or E2) by which each product is formed.
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- Which is an appropriate name for the following compound? (2R,4S)-1,2-epoxy-4-ethoxypentane 2-ероху-4-ethoxypentane O(2R,4R)-1,2-epoxy-4-ethoxypentane (2R,4R)-1,2-ероху-4-еthoxypentane (25,4R)-4,5-epoxy-2-methoxypentane (2R,4S)-1,2-epoxy-4-methyl-5-oxoheptane7 & 8. The major products A, B, and C of the following scheme are: if R Me R PhCH₂OH (1 equiv) cat. H', heat Ph₂P CH₂ major product C if R = H if R-Cl major product A major product B17. Determine the mechanism(s), SN1, SN2, E1 or E2 for the following reaction. Show the step-wise mechanism(s) and determine the product(s). Indicate major product if one is present. Include stereochemistry at stereogenic centers if any are present. (3 products) KOH THF 18. Determine the mechanism for the following reaction (SN1, SN2, E1, or E2). Show the step-wise mechanism and product(s). Determine the major product if one is present. (3 products) OH H₂SO4
- What would be the major product of the following reaction? O CH3 || C6H5C-CHCH3 + D20 A) B) C) D) E) O CD3 C6H5C-CHCH3 O CH3 1-1 C6H5C-CDCH3 O CH3 C6D5C-CDCH3 O CD3 | | C6H5C-CDCD3 OD - C6H5CDCHCH3 CH3 OD room temp. ?Curved arrows are used to illustrate the flow of electrons. Follow the arrows and draw the intermediate and product in this reaction. Include all lone pairs. Ignore stereochemistry. Ignore inorganic byproducts. :O: H :OCH3 H OH CH3 CH3OH2+ protonation CH3OH deprotonation H3C CH3OH ОН nucleophilic addition -H Draw Intermediate QDraw Intermediate CH3OH₂+ protonation H H3C -0 H Q CH3OH deprotonation loss of H₂O elimination H3C :0 ÖH -CH3 Draw Intermediate CH3OH deprotonatio Please select a drawing or reag
- Q2-) Draw a detailed mechanism for the following Fischer esterification reaction.(13 points) A few drops of HSO4 Acetic acid Ethanol Ethyl acetate(h) CHCO CI CH3CO2H, 50 °C Draw the major product(s) of the reaction.(b) Show the mechanism to form 2-chloro-2-methylpentane, but not 2-chloro-4-methylpentane. CI H -CI H -CI
- The conversion of 3 alcohols into alkenes under acidic conditions involves two cationic intermediates. For each reaction, draw the complete mechanism using curved arrows.Complete the reaction by identifying the major product/s of the reaction: NucBase Strength methyl 1 strongistrong SN2 SN2 E2 E2 no strongweak SN2 SN2 SN2 reaction no weak/strong E2 E2 E2 reaction no no weakiweak SNTET SNIEI reaction reaction Br (W) O Il only III only O l only O IV only I and II Il and IIIA common ketone starting material is shown below. Predict the major product for each reaction based on the reagents given. Ignore any inorganic byproducts. Sel ect to Dr aw CH3NH2, pH 4-5 Sel ect to Dr aw 1.NaBH4 2. Neutralizing work-up