Organic Chemistry
Organic Chemistry
5th Edition
ISBN: 9780078021558
Author: Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
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Chapter 7, Problem 7.17P
Interpretation Introduction

(a)

Interpretation: The nucleophile needed to convert (CH3)2CHCH2CH2Br to given product is to be predicted.

Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. The electron rich chemical species that contains negative charge or lone pair of electrons are known as a nucleophile. In a nucleophilic substitution reaction, nucleophile takes the position of leaving group by attacking the electron deficient carbon atom.

Expert Solution
Check Mark

Answer to Problem 7.17P

The nucleophile needed to convert (CH3)2CHCH2CH2Br to given product is SH or H2S.

Explanation of Solution

The reactant of the reaction is (CH3)2CHCH2CH2Br. The structure of the product shows that SH group is present at the place of Br group. Hence, Br acts as a leaving group and SH or H2S acts as a nucleophile during the formation of product. The reaction of (CH3)2CHCH2CH2Br with SH is shown in Figure 1.

Organic Chemistry, Chapter 7, Problem 7.17P , additional homework tip  1

Figure 1

The reaction of (CH3)2CHCH2CH2Br with H2S is shown in Figure 2.

Organic Chemistry, Chapter 7, Problem 7.17P , additional homework tip  2

Figure 2

Conclusion

The nucleophile needed to convert (CH3)2CHCH2CH2Br to given product is SH or H2S.

Interpretation Introduction

(b)

Interpretation: The nucleophile needed to convert (CH3)2CHCH2CH2Br to given product is to be predicted.

Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. The electron rich chemical species that contains negative charge or lone pair of electrons are known as a nucleophile. In a nucleophilic substitution reaction, nucleophile takes the position of leaving group by attacking the electron deficient carbon atom.

Expert Solution
Check Mark

Answer to Problem 7.17P

The nucleophile needed to convert (CH3)2CHCH2CH2Br to given product is OCH2CH3 or HOCH2CH3.

Explanation of Solution

The reactant of the reaction is (CH3)2CHCH2CH2Br. The structure of the product shows that OCH2CH3 group is present at the place of Br group. Hence, Br acts as a leaving group and OCH2CH3 or HOCH2CH3 acts as a nucleophile during the formation of product. The reaction of (CH3)2CHCH2CH2Br with OCH2CH3 is shown in Figure 3.

Organic Chemistry, Chapter 7, Problem 7.17P , additional homework tip  3

Figure 3

The reaction of (CH3)2CHCH2CH2Br with H2S is shown in Figure 4.

Organic Chemistry, Chapter 7, Problem 7.17P , additional homework tip  4

Figure 4

Conclusion

The nucleophile needed to convert (CH3)2CHCH2CH2Br to given product is OCH2CH3 or HOCH2CH3.

Interpretation Introduction

(c)

Interpretation: The nucleophile needed to convert (CH3)2CHCH2CH2Br to given product is to be predicted.

Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. The electron rich chemical species that contains negative charge or lone pair of electrons are known as a nucleophile. In a nucleophilic substitution reaction, nucleophile takes the position of leaving group by attacking the electron deficient carbon atom.

Expert Solution
Check Mark

Answer to Problem 7.17P

The nucleophile needed to convert (CH3)2CHCH2CH2Br to given product is OOCH3 or HOOCH3.

Explanation of Solution

The reactant of the reaction is (CH3)2CHCH2CH2Br. The structure of the product shows that OOCH3 group is present at the place of Br group. Hence, Br acts as a leaving group and OOCH3 or HOOCH3 acts as a nucleophile during the formation of product. The reaction of (CH3)2CHCH2CH2Br with OOCH3 is shown in Figure 5.

Organic Chemistry, Chapter 7, Problem 7.17P , additional homework tip  5

Figure 5

The reaction of (CH3)2CHCH2CH2Br with H2S is shown in Figure 6.

Organic Chemistry, Chapter 7, Problem 7.17P , additional homework tip  6

Figure 6

Conclusion

The nucleophile needed to convert (CH3)2CHCH2CH2Br to given product is OOCH3 or HOOCH3.

Interpretation Introduction

(d)

Interpretation: The nucleophile needed to convert (CH3)2CHCH2CH2Br to given product is to be predicted.

Concept introduction: The replacement or substitution of one functional group with another different functional group in any chemical reaction is termed as substitution reaction. The electron rich chemical species that contains negative charge or lone pair of electrons are known as a nucleophile. In a nucleophilic substitution reaction, nucleophile takes the position of leaving group by attacking the electron deficient carbon atom.

Expert Solution
Check Mark

Answer to Problem 7.17P

The nucleophile needed to convert (CH3)2CHCH2CH2Br to given product is CN.

Explanation of Solution

The reactant of the reaction is (CH3)2CHCH2CH2Br. The structure of the product shows that CN group is present at the place of Br group. Hence, Br acts as a leaving group and CN acts as a nucleophile during the formation of product. The reaction of (CH3)2CHCH2CH2Br with CN is shown in Figure 7.

Organic Chemistry, Chapter 7, Problem 7.17P , additional homework tip  7

Figure 7

Conclusion

The nucleophile needed to convert (CH3)2CHCH2CH2Br to given product is CN.

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Chapter 7 Solutions

Organic Chemistry

Ch. 7 - Prob. 7.11PCh. 7 - Does the equilibrium favor the reactants or...Ch. 7 - Prob. 7.13PCh. 7 - Classify each solvent as protic or aprotic. a. b....Ch. 7 - Prob. 7.15PCh. 7 - Prob. 7.16PCh. 7 - Prob. 7.17PCh. 7 - Prob. 7.18PCh. 7 - Prob. 7.19PCh. 7 - Draw the product of each SN2 reaction and indicate...Ch. 7 - Prob. 7.21PCh. 7 - Prob. 7.22PCh. 7 - What happens to the rate of an SN1 reaction under...Ch. 7 - Draw the products of each SN1 reaction and...Ch. 7 - Classify each carbocation as 1,2, or 3. a. b. c....Ch. 7 - Prob. 7.26PCh. 7 - Prob. 7.27PCh. 7 - Prob. 7.28PCh. 7 - Prob. 7.29PCh. 7 - Problem 7.30 For each alkyl halide and...Ch. 7 - Prob. 7.31PCh. 7 - Prob. 7.32PCh. 7 - Prob. 7.33PCh. 7 - Prob. 7.34PCh. 7 - Prob. 7.35PCh. 7 - Prob. 7.36PCh. 7 - Prob. 7.37PCh. 7 - Prob. 7.38PCh. 7 - Prob. 7.39PCh. 7 - Give the IUPAC name for each compound, including...Ch. 7 - Draw the products formed when each alkyl halide is...Ch. 7 - Give the IUPAC name for each compound. a. c. e. b....Ch. 7 - Prob. 7.43PCh. 7 - Draw the eight constitutional isomers having the...Ch. 7 - Which compound in each pair has the higher boiling...Ch. 7 - Draw the products of each nucleophilic...Ch. 7 - Prob. 7.47PCh. 7 - Rank the species in each group in order of...Ch. 7 - Which of the following nucleophilic substitution...Ch. 7 - Rank the species in each group in order of...Ch. 7 - Prob. 7.51PCh. 7 - Prob. 7.52PCh. 7 - 7.53 Consider the following reaction. Draw a...Ch. 7 - Prob. 7.54PCh. 7 - Draw the products of each SN2 reaction and...Ch. 7 - Prob. 7.56PCh. 7 - Prob. 7.57PCh. 7 - Consider the following SN1 reaction. a.Draw a...Ch. 7 - 7.59 Pick the reactant or solvent in each part...Ch. 7 - Draw the products of each SN1 reaction and...Ch. 7 - Prob. 7.61PCh. 7 - Prob. 7.62PCh. 7 - Prob. 7.63PCh. 7 - Fluticasone, the chapter-opening molecule, can be...Ch. 7 - Prob. 7.65PCh. 7 - 7.66 Diphenhydramine, the antihistamine in...Ch. 7 - Draw a stepwise, detailed mechanism for the...Ch. 7 - When a single compound contains both a nucleophile...Ch. 7 - Prob. 7.69PCh. 7 - Prob. 7.70PCh. 7 - Draw a stepwise, detailed mechanism f or the...Ch. 7 - Prob. 7.72PCh. 7 - Fill in the appropriate reagent or starting...Ch. 7 - Devise a synthesis of each compound from an alkyl...Ch. 7 - Suppose you have compounds A-D at y our disposal....Ch. 7 - Muscalure, the sex pheromone of the common...Ch. 7 - Prob. 7.77PCh. 7 - Prob. 7.78PCh. 7 - Draw a stepwise mechanism for the following...Ch. 7 - 7.80 As we will learn in Chapter 9, an epoxide is...Ch. 7 - Prob. 7.81PCh. 7 - In some nucleophilic substitutions under SN1...
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