ORGANIC CHEMISTRY-PRINT COMPANION (LL)
ORGANIC CHEMISTRY-PRINT COMPANION (LL)
4th Edition
ISBN: 9781119659594
Author: Klein
Publisher: WILEY
Question
Book Icon
Chapter 18.13, Problem 32CC
Interpretation Introduction

Interpretation:

Considering the following reaction as example –

                     ORGANIC CHEMISTRY-PRINT COMPANION (LL), Chapter 18.13, Problem 32CC , additional homework tip  1

  • The lowering of temperature in aromatic nucleophilic substitution reaction when there is increase in number of nitro groups has to be justified.
  • The impact caused by the placement of the fourth nitro group in the above compound in lowering the reaction temperature of aromatic nucleophilic substitution reactions has to be analyzed.

Concept Introduction:

  • Benzene and its compounds undergo a unique type of reactions namely Aromatic nucleophilic substitution reactions designated as SNAr .
  • A nucleophile, unlike an electrophile is a species that is electron rich and always attracted towards electron deficient site. A nucleophile is mobile unlike electrophile. Thus in aromatic nucleophilic substitution reactions the aromatic compound behaves as electron deficient species. The aromatic compound must be deficient of electrons so that it acquires positive charge and attacked by nucleophile.
  • In the mechanism of SNAr reaction the nucleophile attacks the position that is bonded to leaving group and forms a resonance stabilized intermediate called Meisenheimer complex.
  • The criteria for aromatic nucleophilic substitution reaction to occur are –
  • The aromatic ring must contain a strong electron withdrawing group like nitro group.
  • The aromatic ring must contain a leaving group.
  • The leaving group must be posited either ortho or para position to the strong electron withdrawing group.
  • In aromatic compounds the site in the ring where there is deficient of electrons is attacked by the nucleophile. A new C-Nu bond is formed where ‘Nu’ is the nucleophile and ‘C’ is aromatic ring Carbon. In this process the bond between aromatic Carbon and the substituent bonded with it is broken.
  • Let the substituent be ‘X’ that then C-X bond gets broken and  C-Nu bond is formed. The substituent ‘X’ is termed as ‘Leaving group’. A good leaving is large in size with high electron affinity that they are capable to grabbing the bond pair electron and leaving form the aromatic C atom. Halogens are known to be excellent leaving group.
  • The overall reaction can be represented as follows –

                     ORGANIC CHEMISTRY-PRINT COMPANION (LL), Chapter 18.13, Problem 32CC , additional homework tip  2

  • Activation energy is the minimum amount of energy that the reactant must possess to undergo chemical reaction. If the reactant molecules do not possess the minimum energy then the required energy can be supplied externally in the form of heat or some other means.

Blurred answer
Students have asked these similar questions
Complete the mechanism for the E1 reaction below by following the directions written above each of the five boxes. Be sure to include lone pair electrons and nonzero formal charges. 2nd attempt 1 Provide the missing curved arrow notation. E+ RUDDA 1st attempt Feedback See Periodic Table See Hint Iir See Periodic Table See Hint
Heating an alcohol in the presence of sulfuric or phosphoric acid will cause a dehydration to occur: the removal of the elements of water from a molecule, forming an alkene. The reaction usually follows an E1 mechanism. The SN1 pathway is suppressed by using a strong acid whose conjugate base is a poor nucleophile. Further, heating the reaction mixture causes a greater increase in the rate of E1 compared to the rate of Sy1. 3rd attempt h Draw curved arrow(s) to show how the alcohol reacts with phosphoric acid. TH © 1 0 0 +1% # 2nd attempt Feedback H Ju See Periodic Table See Hint H Jud See Periodic Table See Hint
Part 2 (0.5 point) 0- Draw the major organic product with the correct geometry. 10 1: 70000 х く 1st attempt Part 1 (0.5 point) Feedback Please draw all four bonds at chiral centers. P See Periodic Table See Hint

Chapter 18 Solutions

ORGANIC CHEMISTRY-PRINT COMPANION (LL)

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