ORGANIC CHEMISTRYPKGDRL+MLCRL MDL
ORGANIC CHEMISTRYPKGDRL+MLCRL MDL
3rd Edition
ISBN: 9781119416746
Author: Klein
Publisher: WILEY
bartleby

Concept explainers

Question
Book Icon
Chapter 21, Problem 63PP

(a)

Interpretation Introduction

Interpretation: The reagents that are used to make the given compound of aldol condensation have to be found.

Concept Introduction:

Retro synthetic analysis:

It is the analysis of the synthetic starting materials for a given compound through its precursors or fragments which are known as synthons. The synthons can be obtained by logical cleavage of the chemical bonds in the compounds. The resulted synthons will be therefore known as logical synthons.

Crossed aldol condensation:

Crossed aldol condensation reaction occurs, when an aldehyde and a ketone are heated in aqueous sodium hydroxide. The resulted product will be an α,β-unsaturatedaldehydeorketone that forms through elimination of water. The basic reagent NaOH gives a suitable environment for the reactants to involve in the condensation reaction.

General scheme:

ORGANIC CHEMISTRYPKGDRL+MLCRL MDL, Chapter 21, Problem 63PP , additional homework tip  1

Retro aldol analysis:

To obtain the reactants of the given aldol product, the alpha beta unsaturated bond has to be cleaved using water molecule as shown here:

ORGANIC CHEMISTRYPKGDRL+MLCRL MDL, Chapter 21, Problem 63PP , additional homework tip  2

(b)

Interpretation Introduction

Interpretation: The reagents that are used to make the given compound of aldol condensation have to be found.

Concept Introduction:

Retro synthetic analysis:

It is the analysis of the synthetic starting materials for a given compound through its precursors or fragments which are known as synthons. The synthons can be obtained by logical cleavage of the chemical bonds in the compounds. The resulted synthons will be therefore known as logical synthons.

Crossed aldol condensation:

Crossed aldol condensation reaction occurs, when an aldehyde and a ketone are heated in aqueous sodium hydroxide. The resulted product will be an α,β-unsaturatedaldehydeorketone that forms through elimination of water. The basic reagent NaOH gives a suitable environment for the reactants to involve in the condensation reaction.

General scheme:

ORGANIC CHEMISTRYPKGDRL+MLCRL MDL, Chapter 21, Problem 63PP , additional homework tip  3

Retro aldol analysis:

To obtain the reactants of the given aldol product, the alpha beta unsaturated bond has to be cleaved using water molecule as shown here:

ORGANIC CHEMISTRYPKGDRL+MLCRL MDL, Chapter 21, Problem 63PP , additional homework tip  4

(c)

Interpretation Introduction

Interpretation: The reagents that are used to make the given compound of aldol condensation have to be found.

Concept Introduction:

Retro synthetic analysis:

It is the analysis of the synthetic starting materials for a given compound through its precursors or fragments which are known as synthons. The synthons can be obtained by logical cleavage of the chemical bonds in the compounds. The resulted synthons will be therefore known as logical synthons.

Crossed aldol condensation:

Crossed aldol condensation reaction occurs, when an aldehyde and a ketone are heated in aqueous sodium hydroxide. The resulted product will be an α,β-unsaturatedaldehydeorketone that forms through elimination of water. The basic reagent NaOH gives a suitable environment for the reactants to involve in the condensation reaction.

General scheme:

ORGANIC CHEMISTRYPKGDRL+MLCRL MDL, Chapter 21, Problem 63PP , additional homework tip  5

Retro aldol analysis:

To obtain the reactants of the given aldol product, the alpha beta unsaturated bond has to be cleaved using water molecule as shown here:

ORGANIC CHEMISTRYPKGDRL+MLCRL MDL, Chapter 21, Problem 63PP , additional homework tip  6

Blurred answer
Students have asked these similar questions
(a) Sketch the 'H NMR of the following chemical including the approximate chemical shifts, the multiplicity (splitting) of all signals and the integration (b) How many signals would you expect in the 13C NMR? CH3
Draw the Show the major and minor product(s) for the following reaction mechanisms for both reactions and show all resonance structures for any Explain why the major product is favoured? intermediates H-Br
Choose the right answer

Chapter 21 Solutions

ORGANIC CHEMISTRYPKGDRL+MLCRL MDL

Ch. 21.2 - Prob. 10CCCh. 21.2 - Prob. 11CCCh. 21.2 - Prob. 12CCCh. 21.2 - Prob. 13CCCh. 21.3 - Prob. 2LTSCh. 21.3 - Prob. 14PTSCh. 21.3 - Prob. 15PTSCh. 21.3 - Prob. 16ATSCh. 21.3 - Prob. 3LTSCh. 21.3 - Prob. 17PTSCh. 21.3 - Prob. 18ATSCh. 21.3 - Prob. 4LTSCh. 21.3 - Prob. 19PTSCh. 21.3 - Prob. 20ATSCh. 21.3 - Prob. 21CCCh. 21.3 - Prob. 22CCCh. 21.3 - Prob. 23CCCh. 21.4 - Prob. 24CCCh. 21.4 - Prob. 25CCCh. 21.4 - Prob. 26CCCh. 21.4 - Prob. 27CCCh. 21.4 - Prob. 28CCCh. 21.5 - Prob. 29CCCh. 21.5 - Prob. 30CCCh. 21.5 - Prob. 5LTSCh. 21.5 - Prob. 31PTSCh. 21.5 - Prob. 32ATSCh. 21.5 - Prob. 6LTSCh. 21.5 - Prob. 33PTSCh. 21.5 - Prob. 34ATSCh. 21.6 - Prob. 35CCCh. 21.6 - Prob. 36CCCh. 21.6 - Prob. 37CCCh. 21.6 - Prob. 7LTSCh. 21.6 - Prob. 38PTSCh. 21.6 - Prob. 39ATSCh. 21.6 - Prob. 40CCCh. 21.6 - Prob. 41CCCh. 21.7 - Prob. 8LTSCh. 21.7 - Prob. 42PTSCh. 21.7 - Prob. 43PTSCh. 21.7 - Prob. 9LTSCh. 21.7 - Prob. 45PTSCh. 21.7 - Prob. 46ATSCh. 21 - Prob. 47PPCh. 21 - Prob. 48PPCh. 21 - Prob. 49PPCh. 21 - Prob. 50PPCh. 21 - Prob. 51PPCh. 21 - Prob. 52PPCh. 21 - Prob. 53PPCh. 21 - Prob. 54PPCh. 21 - Prob. 55PPCh. 21 - Prob. 56PPCh. 21 - Prob. 57PPCh. 21 - Prob. 58PPCh. 21 - Prob. 59PPCh. 21 - Prob. 60PPCh. 21 - Prob. 61PPCh. 21 - Prob. 62PPCh. 21 - Prob. 63PPCh. 21 - Prob. 64PPCh. 21 - Prob. 65PPCh. 21 - Prob. 66PPCh. 21 - Prob. 67PPCh. 21 - Prob. 68PPCh. 21 - Prob. 69PPCh. 21 - Prob. 70PPCh. 21 - Prob. 71PPCh. 21 - Prob. 72PPCh. 21 - Prob. 73PPCh. 21 - Prob. 74PPCh. 21 - Prob. 75PPCh. 21 - Prob. 76PPCh. 21 - Prob. 77PPCh. 21 - Prob. 78PPCh. 21 - Prob. 79PPCh. 21 - Prob. 80PPCh. 21 - Prob. 81PPCh. 21 - Prob. 82PPCh. 21 - Prob. 83PPCh. 21 - Prob. 84PPCh. 21 - Prob. 85PPCh. 21 - Prob. 86PPCh. 21 - Prob. 87PPCh. 21 - Prob. 88PPCh. 21 - Prob. 89IPCh. 21 - Prob. 90IPCh. 21 - Prob. 91IPCh. 21 - Prob. 92IPCh. 21 - Prob. 93IPCh. 21 - Prob. 94IPCh. 21 - Prob. 95IPCh. 21 - Prob. 96IPCh. 21 - Prob. 97IPCh. 21 - Prob. 98IPCh. 21 - Prob. 99IPCh. 21 - Prob. 100IPCh. 21 - Prob. 101IPCh. 21 - Prob. 102IPCh. 21 - Prob. 103IPCh. 21 - Prob. 104IPCh. 21 - Prob. 105IPCh. 21 - Prob. 106IPCh. 21 - Prob. 107IPCh. 21 - Prob. 108IPCh. 21 - Prob. 109IPCh. 21 - Prob. 110IPCh. 21 - Prob. 111IPCh. 21 - Prob. 112IPCh. 21 - Prob. 113IPCh. 21 - Prob. 114IPCh. 21 - Prob. 115IPCh. 21 - Prob. 116CPCh. 21 - Prob. 117CPCh. 21 - Prob. 118CP
Knowledge Booster
Background pattern image
Chemistry
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
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