Organic Chemistry-Package(Custom)
Organic Chemistry-Package(Custom)
4th Edition
ISBN: 9781259141089
Author: SMITH
Publisher: MCG
bartleby

Concept explainers

Question
Book Icon
Chapter 20, Problem 20.34P
Interpretation Introduction

(a)

Interpretation:

The product formed by the treatment of given compound with either (CH3)2CuLi followed by H2O or HCCLi followed by H2O is to be stated.

Concept introduction:

Organometallic reagents like RLi,RMgX and R2CuLi are the source of R, which acts as a nucleophile. Organocuprate reagent form 1,4-addition product on reaction with α, β-unsaturated carbonyl compound whereas organolithium and Grignard reagent form 1,2-addition product on reaction with α, β-unsaturated carbonyl compound.

Expert Solution
Check Mark

Answer to Problem 20.34P

The product formed by the treatment of given compound with (CH3)2CuLi followed by H2O and HCCLi followed by H2O is,

Organic Chemistry-Package(Custom), Chapter 20, Problem 20.34P , additional homework tip  1

Figure 1

Explanation of Solution

The given reagents are organocuprate ((CH3)2CuLi) and organolithium (HCCLi). Organocuprate reagent form 1,4-addition product whereas organolithium reagent form 1,2-addition product on reaction with α, β-unsaturated carbonyl compound.

The product formed by the reaction of (CH3)2CuLi with given α, β-unsaturated carbonyl compound is 1,4-addition product as shown in Figure 2.

Organic Chemistry-Package(Custom), Chapter 20, Problem 20.34P , additional homework tip  2

Figure 2

The product formed by the reaction of HCCLi with given α, β-unsaturated carbonyl compound is 1,4-addition product as shown in Figure 3.

Organic Chemistry-Package(Custom), Chapter 20, Problem 20.34P , additional homework tip  3

Figure 3

Conclusion

The product formed by the treatment of given compound with (CH3)2CuLi followed by H2O and HCCLi followed by H2O is shown in Figure 2 and Figure 3.

Interpretation Introduction

(b)

Interpretation:

The product formed by the treatment of given compound with either (CH3)2CuLi followed by H2O or HCCLi followed by H2O is to be stated.

Concept introduction:

Organometallic reagents like RLi,RMgX and R2CuLi are the source of R, which acts as a nucleophile. Organocuprate reagent form 1,4-addition product on reaction with α, β-unsaturated carbonyl compound whereas organolithium and Grignard reagent form 1,2-addition product on reaction with α, β-unsaturated carbonyl compound.

Expert Solution
Check Mark

Answer to Problem 20.34P

The product formed by the treatment of given compound with (CH3)2CuLi followed by H2O and HCCLi followed by H2O is,

Organic Chemistry-Package(Custom), Chapter 20, Problem 20.34P , additional homework tip  4

Figure 4

Explanation of Solution

The given reagents are organocuprate ((CH3)2CuLi) and organolithium (HCCLi). Organocuprate reagent form 1,4-addition product whereas organolithium reagent form 1,2-addition product on reaction with α, β-unsaturated carbonyl compound.

The product formed by the reaction of (CH3)2CuLi with given α, β-unsaturated carbonyl compound is 1,4-addition product as shown in Figure 5.

Organic Chemistry-Package(Custom), Chapter 20, Problem 20.34P , additional homework tip  5

Figure 5

The product formed by the reaction of HCCLi with given α, β-unsaturated carbonyl compound is 1,4-addition product as shown in Figure 6.

Organic Chemistry-Package(Custom), Chapter 20, Problem 20.34P , additional homework tip  6

Figure 6

Conclusion

The product formed by the treatment of given compound with (CH3)2CuLi followed by H2O and HCCLi followed by H2O is shown in Figure 5 and Figure 6.

Interpretation Introduction

(c)

Interpretation:

The product formed by the treatment of given compound with either (CH3)2CuLi followed by H2O or HCCLi followed by H2O is to be stated.

Concept introduction:

Organometallic reagents like RLi,RMgX and R2CuLi are the source of R, which acts as a nucleophile. Organocuprate reagent form 1,4-addition product on reaction with α, β-unsaturated carbonyl compound whereas organolithium and Grignard reagent form 1,2-addition product on reaction with α, β-unsaturated carbonyl compound.

Expert Solution
Check Mark

Answer to Problem 20.34P

The product formed by the treatment of given compound with (CH3)2CuLi followed by H2O and HCCLi followed by H2O is,

Organic Chemistry-Package(Custom), Chapter 20, Problem 20.34P , additional homework tip  7

Figure 7

Explanation of Solution

The given reagents are organocuprate ((CH3)2CuLi) and organolithium (HCCLi). Organocuprate reagent form 1,4-addition product whereas organolithium reagent form 1,2-addition product on reaction with α, β-unsaturated carbonyl compound.

The product formed by the reaction of (CH3)2CuLi with given α, β-unsaturated carbonyl compound is 1,4-addition product as shown in Figure 2.

Organic Chemistry-Package(Custom), Chapter 20, Problem 20.34P , additional homework tip  8

Figure 8

The product formed by the reaction of HCCLi with given α, β-unsaturated carbonyl compound is 1,4-addition product as shown in Figure 3.

Organic Chemistry-Package(Custom), Chapter 20, Problem 20.34P , additional homework tip  9

Figure 9

Conclusion

The product formed by the treatment of given compound with (CH3)2CuLi followed by H2O and HCCLi followed by H2O is shown in Figure 8 and Figure 9.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
complete these reactions with reagents and intermediates.
What products result from each step in the following reactions? Use mild acid if needed. q H₂O, H+ TfCl MeOH + + + TfCl MeOH
Draw the major product for the following reaction: 1) 9-BBN 2) H₂O₂, NaOH ?

Chapter 20 Solutions

Organic Chemistry-Package(Custom)

Ch. 20 - Draw the structure of both an acid chloride and an...Ch. 20 - Problem 20.12 Draw the products formed from ...Ch. 20 - Prob. 20.13PCh. 20 - Prob. 20.14PCh. 20 - What product is formed when...Ch. 20 - Prob. 20.16PCh. 20 - Problem-20.16 Review the oxidation reactions using...Ch. 20 - Problem-20.17 Write the step(s) needed to convert ...Ch. 20 - Problem-20.18 Oct-1-yne reacts rapidly with ,...Ch. 20 - Draw the product formed when each organometallic...Ch. 20 - Draw the product of each reaction. a.c. b.d.Ch. 20 - Draw the products including stereochemistry of the...Ch. 20 - What Grignard reagent and carbonyl compound are...Ch. 20 - Problem 20.24 Linalool (the Chapter 9 opening...Ch. 20 - Problem 20.25 What Grignard reagent and carbonyl...Ch. 20 - Prob. 20.26PCh. 20 - Draw the products formed when each compound is...Ch. 20 - What ester and Grignard reagent are needed to...Ch. 20 - What organocuprate reagent is needed to convert...Ch. 20 - What reagent is needed to convert (CH3)2CHCH2CHO...Ch. 20 - Prob. 20.31PCh. 20 - What carboxylic acid formed from each alkyl halide...Ch. 20 - Prob. 20.33PCh. 20 - Prob. 20.34PCh. 20 - Problem 20.35 Synthesize each compound from...Ch. 20 - Prob. 20.36PCh. 20 - 20.37 Devise a synthesis of each alcohol from...Ch. 20 - 20.38 Draw the products formed when pentanal is...Ch. 20 - Prob. 20.39PCh. 20 - Draw the product formed when CH3CH2CH2MgBr is...Ch. 20 - Draw the product formed when (CH3CH2CH2CH2)2CuLi...Ch. 20 - The stereochemistry of the products of reduction...Ch. 20 - Prob. 20.43PCh. 20 - What reagent is needed to convert...Ch. 20 - What reagent is needed to convert...Ch. 20 - Draw the products or each reduction reaction. a....Ch. 20 - Prob. 20.47PCh. 20 - Draw all stereoisomers formed in each reaction. a....Ch. 20 - Prob. 20.49PCh. 20 - 20.46 Treatment of ketone A with ethynylithium...Ch. 20 - 20.47 Explain why metal hydride reduction gives an...Ch. 20 - Prob. 20.52PCh. 20 - 20.49 Identify the lettered compounds in the...Ch. 20 - Prob. 20.54PCh. 20 - Draw a stepwise mechanism for each reaction. a. b.Ch. 20 - Prob. 20.56PCh. 20 - 20.54 Draw a stepwise mechanism for the following...Ch. 20 - What Grignard reagent and aldehyde or ketone are...Ch. 20 - Prob. 20.59PCh. 20 - What ester and Grignard reagent are needed to...Ch. 20 - What organolithium reagent and carbonyl compound...Ch. 20 - 20.59 What epoxide and organometallic reagent are...Ch. 20 - Prob. 20.63PCh. 20 - 20.61 Propose two different methods to synthesize...Ch. 20 - Synthesize each compound from cyclohexanol using...Ch. 20 - Prob. 20.66PCh. 20 - Prob. 20.67PCh. 20 - Devise three different methods to prepare each...Ch. 20 - Convert benzene into each compound. You may also...Ch. 20 - Design a synthesis of each compound from alcohols...Ch. 20 - Synthesize each compound from the given starting...Ch. 20 - 20.69 An unknown compound A (molecular formula )...Ch. 20 - 20.70 Treatment of compound C (molecular formula )...Ch. 20 - 20.71 Treatment of compound E (molecular formula )...Ch. 20 - 20.72 Reaction of butanenitrile () with methyl...Ch. 20 - 20.73 Treatment of isobutene with forms a...Ch. 20 - Prob. 20.77PCh. 20 - Prob. 20.78PCh. 20 - 20.76 Lithium tri-sec-butylborohydride, also known...Ch. 20 - Prob. 20.80PCh. 20 - Prob. 20.81PCh. 20 - Prob. 20.82PCh. 20 - 20.80 Draw a stepwise mechanism for the following...Ch. 20 - Prob. 20.84P
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