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- The following Walden cycle has been carried out. Explain the results, and indicate where Walden inversion occurs.9) A student described the following reaction as "I brominated it then added bulky base with heat". . A What would the different products be for the following different brominating reagents? NBS, Br₂, HBr, HBY/ROORThe conversion of (CH3)3CI to (CH3)2C=CH2 can occur by either a onestepor a two-step mechanism, as shown in Equations [1] and [2].
- [References] Use the References to access important values if needed for this question. Draw the structure of the organic product that is expected when the following compound is treated with concentrated H,SO4. CH3 CH2CCH2CH3 tosH heat HO. • You do not have to consider stereochemistry. • In cases where there is more than one answer, just draw one. ed P. opy aste C. CH4 ChemDoodle Retry Entire Group 3 more group attempts remaining Submit Answer Previous Next Email Instructor Save and(iii) Explain the products in the following addition reactions with mechanism. CH i) Hg(OAC)2 , H,0 CH3 i) BH3,THF CH3 HO ii) NaBH4, MEOH ii) H,O, /NAOH OHDraw the organometallic compound that would be produced by each of the following reactions. (a) (b) (c) Li(s) Mg(s). Br Mg(s) ? Ether Br H,C=c=CH THE THE Br Mg(s). ? (d) (e) 1. Li(s), THF CI Ether Br 2. Cul (f) (g) .CI 1. Li(s), THF ? Br Li(s) ? 2. CuI THE
- 2. Label the following reactions as most likely occuring by an SN1 or SN2 mechanism. Explain your answer. (4 marks) HBr A) HO, CH;CH2OH 'Br B) Na* SCH; CH;CN ‚Br „SCH3Using curved arrows show the mechanism for the hydrohalogenation for thefollowing reaction. Show how the two possible intermediate products are formed and explain why only one product proceeds to form the product. Clearly indicate attackof electrons and full and partial chargesFor the reaction below, give the major produc excess Cl₂ ..) and show the complete stepwise mechanism
