1. Assign the correct mechanism for the process that will predominantly take place in the reactions A-F shown. Your thr...
1. Assign the correct mechanism for the process that will predominantly take place in the reactions A-F shown. Your three choices are: S2 or E2 or (S1+E1) NaCN t-BuOK Br Br DMSO В. A. NaOCH2CH3 Br Cн,CH-оH D. Br heat C. Н-о F NaOCH2CH3 Br Br E Hint: As practice for the exam, make sure that you can CONFIDENTLY draw the structures of all the products formed in these reactions by the predominant mechanisms that you select! a) A: S&2;...
1. Assign the correct mechanism for the process that will predominantly take place in the reactions A-F shown. Your three choices are: SN2 or E2 or (SN1+E1) Hint: As practice for the exam, make sure that you can CONFIDENTLY draw the structures of all the products formed in these reactions by the predominant mechanisms that you select! a) A: SN2; B: E2; C: SN1+E1; D: E2; E: SN2; F: SN1+E1 b) A: E2; B: SN2; C: E2; D: SN2; E:...
Complete the following with the correct products, label Zaitsev and Hofmann, and explain why the reaction is either regioselective or stereoselective. (6 pts.) D -Br Nahi Complete each of the following reactions by adding the starting material, reaction conditions, or all possible product(s) - label major/minor - Sx2. Sx1, E2 or E1. (33 pts.) (CH3),COK DMF C(CH3) NaOH DMSO CH OH heat Ph H+Br NaOCH, H+CHE Ph DMF SK DMF o (only product)
Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. Methanol to + + NaOCH3 NOCH Mothands t º + HOCH • NAGI HOCHZ + NaCl OH NaHCO3 o + H2O + CO2 + Nal a = Proton transfer b = Lewis acid base c = Radical chain substitution d=Radical chain addition e = Electrophilic addition f=E1 Elimination g=E2 Elimination h=Syl Nucleophilic substitution i= Sy2...
1. for each of thenfollowing write S if it is substitue and E if it is elimination. also write R for those that are rearrangement 2. predict which reactions proceed by SN1 SN2 E1 or E2 mechanism 10/2ery due MON Unit 3 HW#2 Chemistry 420 wo Name: 1. For each of the following reactions, write S if it is a substitution and E if it is an elimination. Also write R for all of those that are also rearrangements. +...
Which product(s) would you expect to obtain from each of the following reactions? In each part give the mechanism (Sw1, SN2, E1 or E2) by which each product is formed. Explain your reasoning. (20 pts) 6. a. NaSH OTs DMSO b. CI NaOCH3 C. OMs NaOCH2CH3 d. ON HCECNa e. KOC(CH3).3 CI Br NaOCH2CH3 CH3CH2OHH
Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. OSCH O=O=O cis and trans 0 H3 Hac Aqueous ethanol + HO + HBr н CH3 CH3 a = Proton transfer b = Lewis acid/base c= Radical chain substitution d = Electrophilic addition e=E1 Elimination f=E2 Elimination g=Syl Nucleophilic substitution h = Sy2 Nucleophilic substitution Identify the mechanism by which each of the reactions above...
please only box one answer for each of these questions. HOH • SOCI + SO, HC a = Proton transfer b = Lewis acid base c = Radical chain substitution d = Radical chain addition e = Electrophilic addition f= E1 Elimination g = E2 Elimination h = Syl Nucleophilic substitution = Sy2 Nucleophilic substitution = Electrophilic aromatic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters - for...
] Ph 1. Na + -COLET D CO2Et + Br CH2-Ph NaB 2. (Ph),C-OH + HCI (Ph) C-Cl + H2O a = Proton transfer d = Electrophilic addition e = E1 Elimination f=E2 Elimination g=Syl Nucleophilic substitution h = Sy2 Nucleophilic substitution b = Lewis acid/base c=Radical chain substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 2.
9) Circle the correct answer for each of the questions below. e. Which reacts faster in an Syl reaction? a. Which reacts faster in an Sy2 reaction? CHs CH, CH,CHCHCH, or CH,CH,CCHy Br Br Br b. Which reacts faster in an El reaction? d. Which reacts faster in an E2 reaction? Br Br 10)2-bromobutane will react with OCH, in the present of dimethylsulfoxide, DMSO, as a solvent to create 1-butene and 2-butene by an elimination reaction A) Write the chemical...