29 30 31 30. The relative rates of nucleophilic substitution for the given substrates are as follows:CompoundApprox. Relative rateCH;CH;Br1.0CH;CH;CH,Br0.28(CH3CHCH,Br0.030(CH3), CCH;Br0.00000042A. Each of the reactions above is likely to be Sn2B. Each of the reactions above is likely to be SN1C. The first two reactions follow SN2 and the next two reactions follow SN1D. There is no role of steric factor31. What is the main product of the following reaction?Na* OEtETOHBrtono reactionOEtAв сDE 29. Which of the following statement is correct?A. E2 is a concerted reaction in which bonds break and new bonds form at thesame time in a single stepB. Order of reactivity of alkyl halides towards E2 dehydrohalogenation is foundto be 3° > 2°> 1°C. In E2 elimination different stereoisomer (diastereomer) converts into differentstereo productD. A, B, and CE. A and B

Answered: Image /qna-images/answer/c1feea74-d289-4061-82e5-3f6cd5176c5d.jpg

29. Which of the following statement is correct? A. E2 is a concerted reaction in which bonds break and new bonds form at the same time in a single step B. Order of reactivity of alkyl halides towards E2 dehydrohalogenation is found to be 3° > 2°> 1° C. In E2 elimination different stereoisomer (diastereomer) converts into different stereo product D. A, B, and C E. A and B

29. Which of the following statement is correct? A. E2 is a concerted reaction in which bonds break and new bonds form at the same time in a single step B. Order of reactivity of alkyl halides towards E2 dehydrohalogenation is found to be 3° > 2°> 1° C. In E2 elimination different stereoisomer (diastereomer) converts into different stereo product D. A, B, and C E. A and B

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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