Homework Help is Here – Start Your Trial Now!
Science
Chemistry
40) For a reaction between a thiolate anion and 1-Chloropropane, why is SN2 more favoured than E2 reaction at normal room temperatures? a. Because it yields Zaitsev's product which is more stable then the substituted product. b. Because the substituted product has a stable intermediate. c. Because it takes less amount of energy spent to undergo a nucleophilic attack towards the partially positive alpha carbon and eliminate the leaving group; than to abstract an anti-periplanar proton and form a double bond after the leaving group departs. d. Because the leaving groups of alkyl halides in an SN2 reaction are better leaving groups than E2 substrate leaving groups; thus, less energy is required for SN2 to occur. e. Because it takes less amount of energy spent for a good nucleophile to attack the alpha carbon and eliminate the leaving group than for a weak base to abstract an anti-periplanar proton and form a double bond after eliminating the leaving group. f. Both C & E.

40) For a reaction between a thiolate anion and 1-Chloropropane, why is SN2 more favoured than E2 reaction at normal room temperatures? a. Because it yields Zaitsev's product which is more stable then the substituted product. b. Because the substituted product has a stable intermediate. c. Because it takes less amount of energy spent to undergo a nucleophilic attack towards the partially positive alpha carbon and eliminate the leaving group; than to abstract an anti-periplanar proton and form a double bond after the leaving group departs. d. Because the leaving groups of alkyl halides in an SN2 reaction are better leaving groups than E2 substrate leaving groups; thus, less energy is required for SN2 to occur. e. Because it takes less amount of energy spent for a good nucleophile to attack the alpha carbon and eliminate the leaving group than for a weak base to abstract an anti-periplanar proton and form a double bond after eliminating the leaving group. f. Both C & E.

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
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
See similar textbooks
icon
Related questions
Question
org chem question answer with explanation. ⁴⁰
40) For a reaction between a thiolate anion and 1-Chloropropane, why is SN2 more favoured than E2 reaction at normal room temperatures? a. Because it yields Zaitsev's product which is more stable then the substituted product. b. Because the substituted product has a stable intermediate. c. Because it takes less amount of energy spent to undergo a nucleophilic attack towards the partially positive alpha carbon and eliminate the leaving group; than to abstract an anti-periplanar proton and form a double bond after the leaving group departs. d. Because the leaving groups of alkyl halides in an SN2 reaction are better leaving groups than E2 substrate leaving groups; thus, less energy is required for SN2 to occur. e. Because it takes less amount of energy spent for a good nucleophile to attack the alpha carbon and eliminate the leaving group than for a weak base to abstract an anti-periplanar proton and form a double bond after eliminating the leaving group. f. Both C & E.
Transcribed Image Text:40) For a reaction between a thiolate anion and 1-Chloropropane, why is SN2 more favoured than E2 reaction at normal room temperatures? a. Because it yields Zaitsev's product which is more stable then the substituted product. b. Because the substituted product has a stable intermediate. c. Because it takes less amount of energy spent to undergo a nucleophilic attack towards the partially positive alpha carbon and eliminate the leaving group; than to abstract an anti-periplanar proton and form a double bond after the leaving group departs. d. Because the leaving groups of alkyl halides in an SN2 reaction are better leaving groups than E2 substrate leaving groups; thus, less energy is required for SN2 to occur. e. Because it takes less amount of energy spent for a good nucleophile to attack the alpha carbon and eliminate the leaving group than for a weak base to abstract an anti-periplanar proton and form a double bond after eliminating the leaving group. f. Both C & E.
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps

SEE SOLUTIONCheck out a sample Q&A here
Blurred answer
Knowledge Booster
Atoms
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY
SEE MORE TEXTBOOKS