Pleaes answer a1a, b, and c. Will upvote, guaranteed. Thank you and much appreciation. Full reaction...
Please answer Q2. Will upvote, guaranteed. Thank you and much appreciation. A) Draw the complete mechanism for the following esterification reaction. Please use curved arrows to indicate electron flow. B) Provide the IUPAC name for the final product. 2. OH (311 11
4. Complete the following reaction and answer the questions. 4. Complete the following reaction and answer the questions. 1. (Structure of LAH) Ph 2. HC1, H2O a. Provide a mechanism of the reaction above. b. Provide two more approaches which can yield the same product in the reaction above. Different reagents and starting material are allowed to use. You need to show the reactions to earn full credits.
- Thank you! If possible, please write the full steps of the reaction. I'd appreciate it Predict which reaction in each of the following pairs will have a higher E2:El product ratio and explain why CH, CH, u011 ? CH CH CHBr CLCH.OH (a) CHCH,CHBr CH CH, Nitromethane Write the structure of the major organic product of the reaction of 2-bromopropane with (a) CH CH OH: (b) NaSCH3 in CH CH OH: (c) NaOCH2CH3 in CH CH2OH. Predict which reaction...
Please show ALL work and justify your answer in full sentences. Thanks so much! 3. Identify the product for the reaction. 1. CH,CH,MgCI 2. H20, H со. A) CH:CH2 он 0 B) CH,CHCH2OH C) CHs он 0 D) CHCHOH 4. Give the product for the following reaction. CH:CH Cl 2 H20, H 0 A) 0% CH CHCH OH CH B) CH,CH. CH C) CH CH он CH D) CH2CH, CHCH OH CH2CH
CH3 H 2. In the reaction below, what type of reaction occurred? A. E2 - H₃C B. E1 slow step C. 5 2 HC—C—CI- (-CI) D.S 1 CH3 E. None of above Nuc: CH) → H3C—C—OH HC CH
2) Fill in each of the following boxes with the structure of the major reaction product(s) from each of the following reactions. (28 points total). a) Pd(PPhale NaOH b) + Pd(OA) (CH CHN CN 1. NaBH 2. H2O HH OH но -н H- OH HH OH CH,OH HNO, но NH,OH trace of acid 1. CHI (excess 2. Ag,0 H2O, heat CI 1 CRUS POY Grubbs catalyst) Page 2 of 5
Please show all work. Thank you! 10. An amine is typically a poor leaving group. An amine can be converted to a good leaving group when treated with excess methyl iodide. The iodide salt is converted to the hydroxide salt using silver oxide and upon heating an E2 reaction occurs. This synthetic sequence is usually referred to as the Hofmann elimination. The reaction commonly favors the formation of the least substituted alkene. excess CH 31 R-N(CH), 1 Ag,0 - —...
4. Complete the following reaction and answer the questions. 1. (Structure of LAH) 2. HC1, H2O a. Provide a mechanism of the reaction above. b. Provide two more approaches which can yield the same product in the reaction above. Different reagents and starting material are allowed to use. You need to show the reactions to earn full credits.
Could you please show the full mechanism for this reaction with arrow pushing. Thank you so much! OS 88 N-Br 064-0 NaOH H2O Br Racemic mixture Scheme 1: Formation of epxoycyclohexane starting with cyclohexene.
Determine the product of the following reaction. 1 L CHOCH "CH Br no reaction H DH (D) 8. Which reagent(s) is needed to facilitate the following reaction: (A) H20, (B) 1. Hg(OAc)2 in H2O 2. NaBH4 (C) 1. Hg(OAc), in CH,OH (D) 1.BH; THE 2. NaBH4 2. H2O2, NaOH (E) all of the above would work 9. Which of the following compounds is the final product of the reaction below: CI (A) (B) CHA + 2 mol Cl, in cct...