1. Na toluene reflux + NaCl .OH H₂O + 2. Br2 Br. HBr a = Proton transfer d = Radical chain addition g = E2 Elimination b = Lewis acid/base e = Electrophilic addition h = SN1 Nucleophilic substitution C = Radical chain substitution f = E1 Elimination i = SN2 Nucleophilic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1 2.

6) The substitution reaction below to produce 1-iodobutane was performed using 1-bromobutane at a 0.1 M concentration and sodium iodide at a 0.1 M concentration. What would the rate law be for the reaction below? How would you expect the rate of the reaction to change if a 0.2 M concentration of sodium iodide was used? How would you expect the rate constant to change? Explain. Nal (0.1 M) Br acetone (0.1 M)

A Grades for Angela Winston: CHEM-2 0 0 C ← caps lock 52 Heavy rain soon A Choose the reagent(s) that would be most likely to complete this reaction. - . S Aktiv Chemistry alt app.101edu.co E # D م Aktiv Chemistry 8888 R ه الكاكاك الكاكاك الكاك G B H N ASUS VivoBook OOOO U ل Answered: se the reagent(s) that wou Question 11 of 27 - M الشان K alt L (1586) Oldies music playing from ctrl 1.OsO. (catalytic) 2 NMO Bra HO 1. BH-THE 2 H.O., NaOH الحالات الالالالالكاك الالالال الكاك تات 1. Hg(OAC), M.O 2. NaBH., NaOH ه + enter, shift

Show the organic chemical reaction mechanism of the synthesis of 1-bromobutane from 1-butanol