Organic Chemistry
Organic Chemistry
2nd Edition
ISBN: 9781118452288
Author: David R. Klein
Publisher: WILEY
Question
Book Icon
Chapter 8.7, Problem 13CC
Interpretation Introduction

Interpretation:

Rate of the reaction should be predicted at different concentrations of substrate and reagent for a second order reaction.

Concept introduction:

  • Elimination reaction: In elimination reaction, two substituents are removed from the substrate to give the product in presence of base. Elimination reactions are two types, E1 and E2.
  • E1 reaction: elimination follows stepwise mechanism. Rate of the reaction depends only on substrate concentration.

    r[substrate]

  • E2 reaction: elimination follows concerted pathway of mechanism. Rate of the reaction depends on both substrates as well as reagent concentration.

    r[substrate][base]

  • Elimination of compound in presence of bulky base leads to less substituted alkene, in presence of strong base (not bulky) leads to more substituted alkene.

(b)

Interpretation Introduction

Interpretation:

Rate of the reaction should be predicted at different concentrations of substrate and reagent for a second order reaction.

Concept introduction:

  • Elimination reaction: In elimination reaction, two substituents are removed from the substrate to give the product in presence of base. Elimination reactions are two types, E1 and E2.
  • E1 reaction: elimination follows stepwise mechanism. Rate of the reaction depends only on substrate concentration.

    r[substrate]

  • E2 reaction: elimination follows concerted pathway of mechanism. Rate of the reaction depends on both substrates as well as reagent concentration.

    r[substrate][base]

  • Elimination of compound in presence of bulky base leads to less substituted alkene, in presence of strong base (not bulky) leads to more substituted alkene.

(c)

Interpretation Introduction

Interpretation:

Rate of the reaction should be predicted at different concentrations of substrate and reagent for a second order reaction.

Concept introduction:

  • Elimination reaction: In elimination reaction, two substituents are removed from the substrate to give the product in presence of base. Elimination reactions are two types, E1 and E2.
  • E1 reaction: elimination follows stepwise mechanism. Rate of the reaction depends only on substrate concentration.

    r[substrate]

  • E2 reaction: elimination follows concerted pathway of mechanism. Rate of the reaction depends on both substrates as well as reagent concentration.

    r[substrate][base]

  • Elimination of compound in presence of bulky base leads to less substituted alkene, in presence of strong base (not bulky) leads to more substituted alkene.

Blurred answer
Students have asked these similar questions
Draw a Haworth projection of a common cyclic form of this monosaccharide CH₂OH HO H HO H H OH CH₂OH
Can you explain how I get these here and show the steps plz?
Give the IUPAC name for this compound Hydrocarbon Condensed Formulas Hint C2H5 CH2CH3 expand that in all the formula Part A: (CH3)2CHCH(C2H5)CH2CH2CH3 Give the IUPAC name for this compound. Part B: CH2=C(C2H5)CH2CH2CH3 Give the IUPAC name for this compound. Part C: (CH3)2C=CHC(C2H5)=CH2 Give the IUPAC name for this compound. Part D: CH3C=CCH(C2H5)2 Give the IUPAC name for this compound. Part E: (CH3)3CC=CCH2CH=C(CH3)2

Chapter 8 Solutions

Organic Chemistry

Ch. 8.5 - Prob. 8PTSCh. 8.6 - Prob. 4LTSCh. 8.6 - Prob. 9PTSCh. 8.6 - Prob. 10PTSCh. 8.6 - Prob. 11ATSCh. 8.6 - Prob. 12ATSCh. 8.7 - Prob. 13CCCh. 8.7 - Prob. 14CCCh. 8.7 - Prob. 5LTSCh. 8.7 - Prob. 15PTSCh. 8.7 - Prob. 16ATSCh. 8.7 - Prob. 17ATSCh. 8.7 - Prob. 6LTSCh. 8.7 - Prob. 18PTSCh. 8.7 - Prob. 19ATSCh. 8.7 - Prob. 20CCCh. 8.7 - Prob. 21CCCh. 8.8 - Prob. 7LTSCh. 8.8 - Prob. 22PTSCh. 8.8 - Prob. 23ATSCh. 8.8 - Prob. 24ATSCh. 8.8 - Prob. 25ATSCh. 8.9 - Prob. 26CCCh. 8.9 - Prob. 27CCCh. 8.9 - Prob. 28CCCh. 8.9 - Prob. 8LTSCh. 8.9 - Prob. 29PTSCh. 8.9 - Prob. 31CCCh. 8.10 - Prob. 32CCCh. 8.10 - Prob. 33CCCh. 8.10 - Prob. 9LTSCh. 8.10 - Prob. 34PTSCh. 8.10 - Prob. 35ATSCh. 8.10 - Prob. 36ATSCh. 8.11 - Prob. 37CCCh. 8.11 - Prob. 38CCCh. 8.12 - Prob. 10LTSCh. 8.13 - Prob. 11LTSCh. 8.14 - Prob. 12LTSCh. 8.14 - Prob. 46PTSCh. 8.14 - Prob. 48ATSCh. 8.14 - Prob. 49ATSCh. 8 - Prob. 50PPCh. 8 - Prob. 51PPCh. 8 - Prob. 52PPCh. 8 - Prob. 53PPCh. 8 - Prob. 54PPCh. 8 - Prob. 55PPCh. 8 - Prob. 56PPCh. 8 - Prob. 57PPCh. 8 - Prob. 58PPCh. 8 - Prob. 59PPCh. 8 - Prob. 60PPCh. 8 - Prob. 61PPCh. 8 - Prob. 62PPCh. 8 - Prob. 63PPCh. 8 - Prob. 64PPCh. 8 - Prob. 65PPCh. 8 - Prob. 66PPCh. 8 - Prob. 67PPCh. 8 - Prob. 68PPCh. 8 - Prob. 69PPCh. 8 - Prob. 70PPCh. 8 - Prob. 71PPCh. 8 - Prob. 72PPCh. 8 - Prob. 73PPCh. 8 - Prob. 74PPCh. 8 - Prob. 75PPCh. 8 - Prob. 76PPCh. 8 - Prob. 77IPCh. 8 - Prob. 78IPCh. 8 - Prob. 79IPCh. 8 - Prob. 80IPCh. 8 - Prob. 81IPCh. 8 - Prob. 82IPCh. 8 - Prob. 83IPCh. 8 - Prob. 84IPCh. 8 - Prob. 85IPCh. 8 - Prob. 86IPCh. 8 - Prob. 87IP
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY