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14. Determine if the following statements for SN2 reactions are True (T) or False (F) by circling the appropriate letter. ▪ Does not involve a carbocation intermediate. The rate of the reaction is dependent only on the concentration of the nucleophile. Secondary alkyl halides react faster than primary alkyl halides. . Substitution at a chiral center gives a racemic mixture of products. . T/F T/F T/F T/F

14. Determine if the following statements for SN2 reactions are True (T) or False (F) by circling the appropriate letter. ▪ Does not involve a carbocation intermediate. The rate of the reaction is dependent only on the concentration of the nucleophile. Secondary alkyl halides react faster than primary alkyl halides. . Substitution at a chiral center gives a racemic mixture of products. . T/F T/F T/F T/F

Chemistry
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
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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14. Determine if the following statements for SN2 reactions are True (T) or False (F) by circling the appropriate letter. Substitution at a chiral center gives a racemic mixture of products. ▪ Does not involve a carbocation intermediate. ▪ The rate of the reaction is dependent only on the concentration of the nucleophile. . Secondary alkyl halides react faster than primary alkyl halides. CI Compound A III T/F 15. Provide the only chair conformation of compound A that can undergo an E2 reaction, and determine the major product expected when the elimination reaction is complete. E2 conditions T/F T/F T/F
Transcribed Image Text:14. Determine if the following statements for SN2 reactions are True (T) or False (F) by circling the appropriate letter. Substitution at a chiral center gives a racemic mixture of products. ▪ Does not involve a carbocation intermediate. ▪ The rate of the reaction is dependent only on the concentration of the nucleophile. . Secondary alkyl halides react faster than primary alkyl halides. CI Compound A III T/F 15. Provide the only chair conformation of compound A that can undergo an E2 reaction, and determine the major product expected when the elimination reaction is complete. E2 conditions T/F T/F T/F
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