Organic Chemistry - With Access (Looseleaf) (Custom)
Organic Chemistry - With Access (Looseleaf) (Custom)
4th Edition
ISBN: 9781259726224
Author: SMITH
Publisher: MCG
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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 - With Access (Looseleaf) (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 - With Access (Looseleaf) (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 - With Access (Looseleaf) (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 - With Access (Looseleaf) (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 - With Access (Looseleaf) (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 - With Access (Looseleaf) (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 - With Access (Looseleaf) (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 - With Access (Looseleaf) (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 - With Access (Looseleaf) (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.

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Chapter 20 Solutions

Organic Chemistry - With Access (Looseleaf) (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
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