2) Answer is C). Because in SN2 reaction, rate depends on both concentration of 2-bromo-2-methylpentane as well as CH3CO2-. Hence overall rate become four times on doubling concentration of both.
3) Answer is A). At low temperature substitution takes place.
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A Queetionne2 Conider te B eacn of 2-r 2-me e e wih CHCOr wn Assuming no...
Question 2: Determine in the following examples if the base is strong enough to deprotonate the terminal alkyne. сH, нс. t-BuOK + Cн Question 3: A terminal alkyne is prepared by treating the dihalide with excess (xs) sodium amide, followed by water. Predict the major product and draw a mechanism for its formation: Br 1) xs NaNHNH 2) Hо Br Identify reagents that you could use to achieve the following transformations: CH3 Нас Н,с CH3 CH3 HyC Н.с CHs CH3...
Problem 13. Write a bond-line formula for each of the following compounds. (a) (E)-1,4-dibromopent-2-ene (b) (R)-3-chloro-2-methylbut-l-ene Problem 14. You have the task of preparing styrene (C.HSCH=CH;) by dehydrohalogenation of either 1- bromo-2-phenylethane or 1-bromo-1-phenylethane using KOH in ethanol at reflux temperature. Which halide would you choose as your starting material to give the better yield of the alkene Explain your answer. Problem 15. The reactions below are unlikely to occur as described. Predict the true major product and the reaction...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...