4. (20 points) There are two reactions given. (Note the arrow pointing to the right and...
1-) What is the difference between SN1 and SN2 reactions? Please list at least three different factors for each reaction type. Also provide an example for each type with detailed arrow-pushing mechanism. 2-) Ethanol is not usually a solvent used for SN2 reactions – why not? Describe an undesirable side reaction that might occur using ethanol as a solvent that would not occur if THF was used as the solvent.
23. Please answer the questions regarding to the following reactions. (12 pts) (a) CI + T (1) Is this a substitution or elimination reaction? (2) Do you think the reaction mechanism is Snl or Sx2? (3) Please provide mechanisms by using curved arrow pushing (step by step) that account for the product CL V ai + H2O (1) Is this a substitution or elimination reaction? (2) Do you think the reaction mechanism is Snl or Sn2? (3) Please provide mechanisms...
Draw the mechanisms of each of the reactions including all electrons and arrow pushing H.SO H.0 1. BH. THE 2. H202, NaOH One H,SO H2O 1. Hg(OAc), H,0 2. NaBH H3PO4 H20
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and under SN2 reaction conditions. Explain your answer. mer 2. Draw the complete mechanism and the products for of the following SN1 reaction paying close attention to stereochemistry. H3C CI CH OH CH2CH3 општироотип солио 3. Provide the product/s for the following reactions. Indicate if the reactions proceed via an SN1, or SN2 mechanism. Indicate proper stereochemistry if it is applicable. Show the mechanisms NaCN...
1. (20 points) Provide the products for the following reactions. Provide stereochemistry where necessary. Determine whether they are SN2, S1, E2, E1, or Elcb where necessary. NO NEED FOR MECHANISMS. Br NaOCH.CH diethyl ether KOBU DMSO heat NaCN THF
3. Provide a full arrow-pushing mechanism for each of the following reactions. Wood CHAMBRE Cascos - LX i. CH3MgBr (excess) ii. H+ OH OCH; 4. Provide the major product of the following reaction and provide a mechanism for its formation. HO1 OH A 5. You need to synthesize a large amount of molecule C, and you have just enough of each of molecules A and B in your chemical inventory. Provide a synthetic route showing how you can efficiently synthesize...
provide a detailed reaction mechanism for each of the reactions below. use curved arrow notation to describe the flow of electrons. you do not need to show resonance stabilization of intermediates. To0-H HaC CH Nao DEL notu NaDEt: NAD CHauhs ELOHE CH CHAuh CH
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
can u provide stepwise mechanisms for questions with electron arrow pushing thank you 9. Give the MAJOR organic product(s) for each of the following reactions. Be sure to clearty stereochemistry where appropriate. If no reaction occurs, so indicate (N.R.) and briejly explain win [4 points each] indicate a) H2 (1 eq) Ph b) H.ot Ph MgBr c) Cl 2) H20 d) H3CO NaBH4 CH3OH e) 끄LiAIH 2) H2O NH 1) CHaLi
Please show all work for Number 5: CH3OH and number 3, HF one. Thank you Complete the following reaction and provide forget resonance structures when applicable. a. a detailed arrow-pushing mechanism. Don't HF OH 5. (28 pt.) Complete the following reactions with the correct structures of starting material or product(s) Indicate 'major' and 'minor' if applicable. Don't forget to specify the stereochemistry and draw both enantiomers if applicable. Provide mechanism only if indicated. Cl2/H20 Et AV Use the provided template...