3. For the following reaction: NaOH DMSO ? a. identify the type of alkyl halide: b. identify the type of nucleophile/base: c. predict the anticipated mechanism(s): d. predict the major organic product by drawing the appropriate mechanism:
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- Br CH₂ONa CH₂OH ? a. Identify the type of alkyl halide: b. Identify the type of nucleophile/base: c. Predict the anticipated mechanism: d. Draw the predicted mechanism(s). If more than one product is possible for a mechanism, draw the mechanism for each product. 2. For the following reaction: CH2CH₂ONa Br CH₂CH₂OH ? a. Identify the type of alkyl halide: b. Identify the type of nucleophile/base: c. Predict the anticipated mechanism: d. Draw the predicted mechanism(s). If more than one product is possible for a mechanism, draw the mechanism for each product.5. For the following reaction: Br CH₂S™ Na+ DMSO a. identify the type of alkyl halide: b. identify the type of nucleophile/base: c. predict the anticipated mechanism: d. predict the major organic product by drawing the appropriate mechanism(s): 7. For the following reaction: Br CH₂O¯ Na* DMSO ? a. identify the type of alkyl halide: b. identify the type of nucleophile/base: c. predict the anticipated mechanism: d. predict the major organic product by drawing the appropriate mechanism(s):Draw the full electron pushing mechanism for the reaction depicted including ALL intermediates (with lone pairs and formal charges). Clearly label the electrophile and nucleophile in each step where appropriate.
- Draw the major organic product for each of the hydroboration-oxidation reactions. Disregard stereochemistry. Draw the product of Reaction A. Select Draw Rings More ||||||CH|OB Reaction A. 1. B₂H6 2. H₂O₂ (aq) 3M NaOH Reaction B. 1. B₂H6 2. H₂O₂ (aq) 3M NaOH S 3 Draw the product in reaction B. Select Draw Rings More |||||||||CH|OB Erase Q2Q Erase Q2Q3. Draw the reaction mechanism for the following reactions. When possible, label nucleophiles/electrophiles, carbocations, and oxonium ions. H* CI. a) H. + H2O + НОCHЗ H* OH H* H;C1. Give the major product(s) of the following reactions as needed. Include any stereoisomers. NaOEt 1. Br NaOH Br 2. NaOtBu 3. A MEOH 4. Br 2. Which reaction will proceed faster A or B? H,S H2S "CI .... в
- Predict the major substitution products of the following reaction. Br. H Na OAc HOAC • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If there is more than one major product possible, draw all of them. H.C. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate multiple products using the sign from the drop-down menu. Q24 DO-Sall ⒸY 981 BEH O. IF1. Consider the following reaction. CI EtOH OEt a. Provide a reasonable arrow-pushing mechanism for the following reaction, showing all steps and balancing all charges. b. Predict the stereochemistry of the final product(s). c. Label the electrophilic sites on the molecule and explain why only one of them undergoes substitution.The reaction will proceed with mechanism because the secondary alkyl halide react with nucleophile. + NaOCH3 Br CH3 O a. SN2, strong O b. SN1, strong O c. SN1, weak O d. SN2, weak
- For the following reaction, H2O a. List all expected organic and covalent products. b. Indicate what mechanism is followed as either Sn1 or Sn2. c. For each organic product, write out a mechanism using arrow notation and any necessary transition states. Remember to include stereochemistry where necessary and required.Predict the major organic product of the given reaction. Select Draw Rings More 1. NaOEt/ETOH 2. CH3CH2CH2Br 3. dilute NaOH/heat 4. H3O* 5. Нeat d orrow mechanism for the scheme by adding any missing atoms, bonds, charges,4. Please write out the general mechanism for the electrophilic addition to alkene. (two steps mechanisum, E+: electrophile, Nuc: nucleophile)