What type of mechanism are the given reactions most likely to follow? What type of mechanism...
3. Predict the major product (only one product) in each of the following reactions and indicate the type of mechanism. (3 pts; no partial point) Mechanism SN2 Sn1 HO HBr 0°C, H20 E2 E1 Mechanism Sn2 Sn1 H2SO4 E2 E1 Mechanism HBr Sn2 Sn1 rt, H20 E2 E1
3. Predict the major product (only one product) in each of the following reactions and indicate the type of mechanism. 3. Predict the major product (only one product) in each of the following reactions and indicate the type of mechanism. (3 pts; no partial point) Mechanism Sn2 Sn1 HO HBr moy ng heo 0°C, H2O E2 E1 Mechanism Sn2 Sn1 H2SO4 E2 E1 Mechanism HBr SN2 Sn1 rt, H20 E2 E1 OH
Tell whether each of the following reactions are likely to be Sn1, Sn2, E1, E1CB, or E2 and provide a mechanism for the transformation in part a. Tell whether each of the following reactions is likely to be Sn1, Sn2, E1, E1cB, or E2: кон Ethanol Br нсон H20
Predict the major product (only one product) in each of the following reactions and indicate the type of mechanism. Mechanism SN2 SN1 НО. HBr 0°С, НаО E2 Е1 Mechanism ОН SN2 SN1 H2SO4 Е2 Е1 Mechanism SN2 SN1 HBr D rt, H2O E2 Е1 ОН
4. Sn1 reactions are unimolecular and Sn2 reactions are bimolecular. What does this mean? Write the generic rate laws for Sn1 and Sn2 reactions. Which reagents do the rates of Sn1 and Sn2 reactions depend on? 5. Consider tert-butylchloride and 2-chloropropane. Which of these compounds is more likely to react via an Sn1 mechanism? Which is more likely to reactive via an Sn2 mechanism? Explain your answer. 6. Rank the following compounds in order of increasing likelihood of undergoing substitution...
7 ་་་་་༌་ཨ་མ་་་་སམ་ What is the most likely mechanism for the following reaction? OET EtOII What is the most likely mechanism for the following reaction? OEt EtOH Br Multiple Choice O SNI Saved . Multiple Choice Ο SN1 Ο SN2 Ο
Q. Predict mechanism type (SN1, E1, SN2, E2) for the following reactions. If more than one is possible, predict which mechanism is more likely and explain why. 5 - HI ح . 0H SNI KOCH2CH3 KOCHCH - I want to wors. NaOH, H2O, 100°C في NaCN ي . HO )..NC دا SN2
20. Arrange the following molecules based on their reactivity for SN1 mechanism (the most reactive to the least reactive) [4pts] Br Br CH3Br Br 21. Considering the SN1, SN2, E1, and E2 mechanisms, the energy diagram shown below corresponds to [4Pts] a. only the SN1 mechanism b. only the E1 mechanism c. both the SN2 and E2 mechanisms d. only the SN2 mechanism. e. only the E2 mechanism f. both the SN1 and El mechanisms energy rxn coordinate 22. If...
4. Predict the products of the following reactions & indicate whether they are most likely to go through an SN2, SN1, E1, or E2 mechanism. NaCN DMSO NaOH CH3OH heat Only one product is formed in the following E2 elimination reaction. Draw an arrow-pushing mechanism for the reaction and provide the correct product structure. Include a 3-D drawing (chair conformation) displaying proper stereochemistry of the transition state to explain formation of only the major product. CH3 •Br NaOCH3 ~"'CHS
8. complete the following reactions. mention the type of mechanism (SN1,SN2, E1, or E2) that each follows 8. Complete the following reactions. Mention the type of mechanism (SNI, SN2, E1 or E2) that each reaction follows. (4) (CHy)COH 100°C Br a) Cl Xiocn, NaOCH3 Heat CH3 b) Cl CH3ONa CH3OH,100°C CH3