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

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...

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