Organic Chemistry
Organic Chemistry
5th Edition
ISBN: 9780078021558
Author: Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
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Chapter 20, Problem 20.38P

Draw the products formed when pentanal ( CH 3 CH 2 CH 2 CH 2 CHO ) is treated with each reagent. With some reagents, no reaction occurs.

a. NaBH 4 , CH 3 OH

b. LiAlH 4 , H 2 O

c. H 2 ( 1 equiv ) , Pd C

d. PCC

e. Na 2 Cr 2 O 7 , H 2 SO 4 , H 2 O

f. Ag 2 O , NH 4 OH

g. [ 1 ] CH 3 CH 2 MgBr , [ 2 ] H 2 O

h. [ 1 ] C 6 H 5 Li , [ 2 ] H 2 O

i. [ 1 ] ( CH 3 ) CuLi , [ 2 ] H 2 O

j. HC CNa , [ 2 ] H 2 O

k. H 3 CC CLi , H 2 O

l. The [product in (a), then TBDMS-Cl, imidazole.

Expert Solution
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Interpretation Introduction

(a)

Interpretation: The product formed by the reaction of pentanal with NaBH4, CH3OH is to be predicted.

Concept introduction: The substitution reaction involves the replacement of one functional group by other functional group. In nucleophilic substitution an electron rich species attack the species that is deficient in electrons. The electrophile and the leaving group together form a substrate. The nucleophile attacks over the substrate and there occurs the removal of leaving group from the substrate.

Answer to Problem 20.38P

The product formed by the reaction of pentanal with NaBH4, CH3OH is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  1

Figure 1

Explanation of Solution

The reaction that shows the formation of product when pentanal reacts with NaBH4, CH3OH is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  2

Figure 2

In the given reaction, sodium borohydride is used as a reducing agent. Sodium borohydride is used to for the reduction of carbonyl compounds to alcohols.

Conclusion

The product formed by the reaction of pentanal with NaBH4, CH3OH is shown in Figure 1.

Expert Solution
Check Mark
Interpretation Introduction

(b)

Interpretation: The product formed by the reaction of pentanal with LiAlH4, H2O is to be predicted.

Concept introduction: The substitution reaction involves the replacement of one functional group by other functional group. In nucleophilic substitution an electron rich species attack the species that is deficient in electrons. The electrophile and the leaving group together form a substrate. The nucleophile attacks over the substrate and there occurs the removal of leaving group from the substrate.

Answer to Problem 20.38P

The product formed by the reaction of pentanal with LiAlH4, H2O is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  3

Figure 1

Explanation of Solution

The reaction that shows the formation of product when pentanal reacts with LiAlH4, H2O is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  4

Figure 3

In the given reaction, LiAlH4 is used as a reducing agent. Lithium aluminium hydride is used to for the reduction of carbonyl compounds to alcohols.

Conclusion

The product formed by the reaction of pentanal with LiAlH4, H2O is shown in Figure 1.

Expert Solution
Check Mark
Interpretation Introduction

(c)

Interpretation: The product formed by the reaction of pentanal with the H2(1equiv), PdC is to be predicted.

Concept introduction: Addition of hydrogen takes place across a double bond of alkenes to form alkanes. This process is known as hydrogenation. It takes place in the presence of catalysts such as nickel, platinum or palladium.

Answer to Problem 20.38P

The product formed by the reaction of pentanal with the H2(1equiv), PdC is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  5

Figure 1

Explanation of Solution

The reaction that shows the formation of product when α,β unsaturated ketone reacts with H2(1equiv), PdC is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  6

Figure 4

In the given reaction, hydrogenation of alkene takes place in the presence of palladium.

Conclusion

The product formed by the reaction of pentanal with the H2(1equiv), PdC is shown in Figure 1.

Expert Solution
Check Mark
Interpretation Introduction

(d)

Interpretation: The product formed by the reaction of pentanal with PCC is to be predicted.

Concept introduction: PCC is an oxidizing reagent and is used for the conversion of alcohols to carbonyl compounds.

Answer to Problem 20.38P

No product is formed by the reaction of pentanal with PCC.

Explanation of Solution

The product formed by the reaction of pentanal with PCC is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  7

Figure 5

Conclusion

No product is formed by the reaction of pentanal with PCC.

Expert Solution
Check Mark
Interpretation Introduction

(e)

Interpretation: The product formed by the reaction of pentanal with the Na2Cr2O7, H2SO4, H2O is to be predicted.

Concept introduction: Organometallic reagents like RLi,RMgX and R2CuLi are the source of R, which acts as a nucleophile. Epoxide converts into alcohol on treatment with organometallic reagents.

Answer to Problem 20.38P

The product formed by the reaction of pentanal with the Na2Cr2O7, H2SO4, H2O is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  8

Figure 6

Explanation of Solution

The product formed by the reaction of pentanal with the Na2Cr2O7, H2SO4, H2O is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  9

Figure 7

Conclusion

The product formed by the reaction of pentanal with the Na2Cr2O7, H2SO4, H2O is shown in Figure 6.

Expert Solution
Check Mark
Interpretation Introduction

(f)

Interpretation: The product formed by the reaction of pentanal with Ag2O,NH4OH is to be predicted.

Concept introduction:

Answer to Problem 20.38P

The product formed by the reaction of pentanal with Ag2O,NH4OH is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  10

Figure 6

Explanation of Solution

The product formed by the reaction of pentanal with Ag2O,NH4OH is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  11

Figure 8

Conclusion

The product formed by the reaction of pentanal with Ag2O,NH4OH is shown in Figure 6.

Expert Solution
Check Mark
Interpretation Introduction

(g)

Interpretation: The product formed by the reaction of pentanal with the [1]CH3CH2MgBr, [2]H2O is to be predicted.

Concept introduction: Grignard reagent is prepared by the reaction of alkyl or aryl bromide with magnesium metal in the presence of ether. The reaction of Grignard reagent with an aldehyde/ketone followed by hydrolysis yields an alcohol.

Answer to Problem 20.38P

The product formed by the reaction of pentanal with the [1]CH3CH2MgBr, [2]H2O is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  12

Figure 9

Explanation of Solution

The reaction that shows the formation of product when α,β unsaturated ketone reacts with [1]CH3CH2MgBr, [2]H2O is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  13

Figure 10

In the given reaction, Grignard reagent is used. This reagent attacks on the carbonyl compound to form alkoxides. In the next step, protonation with water takes place to give the final product.

Conclusion

The product formed by the reaction of pentanal with the [1]CH3CH2MgBr, [2]H2O is shown in Figure 9.

Expert Solution
Check Mark
Interpretation Introduction

(h)

Interpretation: The product formed by the reaction of pentanal with [1]C6H5Li, [2]H2O is to be predicted.

Concept introduction: Organometallic reagents like RLi,RMgX and R2CuLi are the source of R, which acts as a nucleophile. Epoxide converts into alcohol on treatment with organometallic reagents.

Answer to Problem 20.38P

The product formed by the reaction of pentanal with [1]C6H5Li, [2]H2O is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  14

Figure 11

Explanation of Solution

The reaction that shows the formation of product when α,β unsaturated ketone reacts with [1](CH2CH)2CuLi, [2]H2O is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  15

Figure 12

Conclusion

The product formed by the reaction of pentanal with [1]C6H5Li, [2]H2O is shown in Figure 11.

Expert Solution
Check Mark
Interpretation Introduction

(i)

Interpretation: The product formed by the reaction of pentanal with [1](CH3)CuLi, [2]H2O is to be predicted.

Concept introduction: Organometallic reagents like RLi,RMgX and R2CuLi are the source of R, which acts as a nucleophile. Epoxide converts into alcohol on treatment with organometallic reagents.

Answer to Problem 20.38P

No product formed by the reaction of pentanal with [1](CH3)CuLi, [2]H2O is shown below.

Explanation of Solution

The product formed by the reaction of pentanal with [1](CH3)CuLi, [2]H2O is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  16

Figure 13

Aldehydes do not react with organo copper reagent because these reagents are less reactive and cannot attack to the electrophilic centre of the aldehyde group.

Expert Solution
Check Mark
Interpretation Introduction

(j)

Interpretation: The product formed by the reaction of pentanal with HCCNa, [2]H2O is to be predicted.

Concept introduction: Organometallic reagents like RLi,RMgX and R2CuLi are the source of R, which acts as a nucleophile. Epoxide converts into alcohol on treatment with organometallic reagents.

Answer to Problem 20.38P

The product formed by the reaction of pentanal with HCCNa, [2]H2O is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  17

Figure 14

Explanation of Solution

The product formed by the reaction of pentanal with HCCNa, [2]H2O is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  18

Figure 15

Expert Solution
Check Mark
Interpretation Introduction

(k)

Interpretation: The product formed by the reaction of pentanal with H3CCCLi, H2O is to be predicted.

Concept introduction: Organometallic reagents like RLi,RMgX and R2CuLi are the source of R, which acts as a nucleophile. Epoxide converts into alcohol on treatment with organometallic reagents.

Answer to Problem 20.38P

The product formed by the reaction of pentanal with H3CCCLi, H2O is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  19

Figure 16

Explanation of Solution

The reaction that shows the formation of product when α,β unsaturated ketone reacts with [1](CH2CH)2CuLi, [2]H2O is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  20

Figure 17

Expert Solution
Check Mark
Interpretation Introduction

(l)

Interpretation: The product formed by the reaction of pentanal with NaBH4, CH3OH and then TBDMSCl is to be predicted.

Concept introduction: Organometallic reagents like RLi,RMgX and R2CuLi are the source of R, which acts as a nucleophile. Epoxide converts into alcohol on treatment with organometallic reagents.

Answer to Problem 20.38P

The product formed by the reaction of pentanal with NaBH4, CH3OH and then TBDMSCl is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  21

Figure 18

Explanation of Solution

The product formed by the reaction of pentanal with NaBH4, CH3OH and then TBDMSCl is shown below.

Organic Chemistry, Chapter 20, Problem 20.38P , additional homework tip  22

Figure 19

In the given reaction, sodium borohydride is used as a reducing agent. Sodium borohydride is used to for the reduction of carbonyl compounds to alcohols.

Conclusion

The product formed by the reaction of pentanal with the [1]CH3CH2MgBr, [2]H2O is shown in Figure 9.

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Chapter 20 Solutions

Organic Chemistry

Ch. 20 - Prob. 20.11PCh. 20 - Problem 20.12 Draw the products formed from ...Ch. 20 - Prob. 20.13PCh. 20 - Prob. 20.14PCh. 20 - Prob. 20.15PCh. 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 - Prob. 20.19PCh. 20 - Prob. 20.20PCh. 20 - Problem 20.21 Draw the product of each reaction. ...Ch. 20 - Problem 20.22 Draw the products (including...Ch. 20 - Problem 20.23 What Grignard reagent and carbonyl...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 - Problem 20.28 What ester and Grignard reagent are...Ch. 20 - Prob. 20.29PCh. 20 - Problem 20.30 What reagent is needed to convert ...Ch. 20 - Prob. 20.31PCh. 20 - What carboxylic acid formed from each alkyl halide...Ch. 20 - Prob. 20.33PCh. 20 - Problem 20.34 Draw the product when each compound...Ch. 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 - 20.39 Draw the product formed when is treated...Ch. 20 - The stereochemistry of the products of reduction...Ch. 20 - Prob. 20.41PCh. 20 - 20.42 Draw the products or each reduction...Ch. 20 - Prob. 20.43PCh. 20 - 20.44 Draw all stereoisomers formed in each...Ch. 20 - Prob. 20.45PCh. 20 - 20.46 Treatment of ketone A with ethynylithium...Ch. 20 - 20.47 Explain why metal hydride reduction gives an...Ch. 20 - Prob. 20.48PCh. 20 - 20.49 Identify the lettered compounds in the...Ch. 20 - Prob. 20.50PCh. 20 - 20.51 Draw a stepwise mechanism for the following...Ch. 20 - 20.52 Draw a stepwise mechanism for the following...Ch. 20 - Prob. 20.53PCh. 20 - 20.54 Draw a stepwise mechanism for the following...Ch. 20 - Prob. 20.55PCh. 20 - Prob. 20.56PCh. 20 - 20.57 What ester and Grignard reagent are needed...Ch. 20 - 20.58 What organolithium reagent and carbonyl...Ch. 20 - 20.59 What epoxide and organometallic reagent are...Ch. 20 - Prob. 20.60PCh. 20 - 20.61 Propose two different methods to synthesize...Ch. 20 - 20.62 Synthesize each compound from cyclohexanol...Ch. 20 - 20.63 Convert propan-2-ol into each compound....Ch. 20 - 20.64 Convert benzene into each compound. You may...Ch. 20 - 20.65 Design a synthesis of each compound from...Ch. 20 - 20.66 Synthesize each compound from the given...Ch. 20 - Prob. 20.67PCh. 20 - Prob. 20.68PCh. 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 - 20.74 Draw a stepwise mechanism for the following...Ch. 20 - Prob. 20.75PCh. 20 - 20.76 Lithium tri-sec-butylborohydride, also known...Ch. 20 - Prob. 20.77PCh. 20 - Prob. 20.78PCh. 20 - Prob. 20.79PCh. 20 - 20.80 Draw a stepwise mechanism for the following...Ch. 20 - Prob. 20.81P
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