give the major product and mechanism used. label leaving group, solvent and Nucliphile and also identify what reactio...
give the major product of the reaction, and classify leaving group, Substrate, and whether it is an SN1, SN2, E1, or E2 reaction. (Show arrow pushing). KOCH.CH HOCH.CH
give the major product and identify LG, Nucliphile, solvent and whether the reaction is SN1,SN2, E1, or E2 bosc KOCHZ DMSO, A
Predict the major product for the following reaction. Label whether the reaction will proceed through an SN2, Sn1, E2, or E1 mechanism. SN2 / S1/E2/E1 сн. Br NaCN (1 mol) (1 mol) Predict the major product for the following reaction. Label whether the reaction will proceed through an SN2, SN1, E2, or E1 mechanism. SN27 SN1/E2/E1 NaOCH; Сн,он Draw the line structures of the reactants below and predict the product of their reaction. Label the reaction as SN1, SN2, E1,...
**WRITTEN WORK** For the following set of reaction conditions, use the table to identify which mechanism is favored by each factor and which is favored overall. Also, supply the major product. NOC(CH) Acetone, SN1 SN2 EI E2 Factor Strength Concentration Leaving group Solvent Heat Total HTML Edit
Draw the major product and label as SN2, SN1, E2, or E1 7. Draw the major products of the following reactions, and label the reaction as SN2, SN1, E2 E1. (Darkly shaded bonds are wedged) Br NaOMe NaCN H2SO4 OTs NaSH OTs H20 NaOMe Br KOtBu OH HBr HBr OH
16. Give the major product that you would expect to be formed in each of the following reactions. If you think there is no reaction write NR after the arrow. In each case give the mechanism (SN1, SN2, E1 or E2) by which the product is formed. Also indicate the correct stereochemistry when applicable. Both product and the mechanism should be correct to get credit. No partial credit. Nal -BuOK Acetone t-Buo NaSH DMF Br, H NaOMe DMSO MeOH,rt t-BuOH...
Given that the SN2 mechanism requires the nucleophile to force out the leaving group, what would you expect the product ratio of alkyl bromide to alky chloride be when sulfuric acid is the solvent? Also given that the SN1 mechanism requires the nucleophile to react with an empty p orbital of a carbocation involving bond formation, what would you expect the product ratio of alkyl bromide to alky chloride be when sulfuric acid is the solvent? R-Br > R-Cl or...
(3 pt) For the following reactions: a) Label the substrate (1°, 2°, 3°), reagent (Good/Poor Nu, Strong/Weak Base) and solvent (protic, aprotic). b) Determine what mechanism will predominate (SN1, SN2, E1, or E2). c) Draw the product(s) you would expect to form, paying attention to regioselectivity and stereoselectivity. 4. (3 pt) For the following reactions: a) Label the substrate (1º, 2º, 3º), reagent (Good/Poor Nu, Strong/Weak Base) and solvent (protic, aprotic). b) Determine what mechanism will predominate (SN1, SN2, E1,...
(8 pts) For each reaction, predict what mechanism will account for the major product(s) formed and write (SN1, SN2, E1, E2 or N.R.) in the boxes provided. Explanations or drawings are NOT required. 4. а. Н-о Br heat b. OTs NaOEt НOE с. NaCl OTs DMSO d. CI CHон
Thank you so much! (2 pts) Draw the major elimination products and Identify the mechanism responsible (E1 or E2). If both E and Z isomers form, only draw the E alkene. If only one isomer forms, label the alkene "E,""Z," or neither 1. NaOCH3 а. Br НОСHЗ b. НОСНЗ C. CI NaOCH3 d. (6 pts) Draw the substitution and/or elimination product(s) for the following reactions and identify 2. the mechanism responsible (SN1, SN2, E1, or E2) for each product drawn....