The accomplishment of the given transformation by the use of nitrile as an intermediate is to be shown. Concept introduction: The lithium aluminium hydride reduction of nitrile followed by hydrolysis gives primary amine .

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Answer 1

Question

Chapter 21.14, Problem 21.39P

(a)

Interpretation Introduction

Interpretation:

The accomplishment of the given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

The lithium aluminium hydride reduction of nitrile followed by hydrolysis gives primary amine.

(b)

Interpretation Introduction

Interpretation:

The accomplishment of given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

Grignard reagent is used to generate R− carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

(c)

Interpretation Introduction

Interpretation:

The accomplishment of given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

Grignard reagent is used to generate R− carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

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What is the missing reactant in this organic reaction? + R -A HO IN + H₂O Specifically, in the drawing area below draw the skeletal ("line") structure of R. If there is more than one reasonable answer, you can draw any one of them. If there is no reasonable answer, check the No answer box under the drawing area. Note for advanced students: you may assume no products other than those shown above are formed. Explanation Check Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center

Stuc X ctclix ALE X A ALE אן A ALEX Lab (195 X Nut x M Inb x NU X NUT X Unt x + → C www-awu.aleks.com/alekscgi/x/Isl.exe/10_u-lgNslkr7j8P3jH-IQ1g8NUi-mObKa_ZLx2twjEhK7mVG6PulJI006NcKTV37JxMpZuyrVCdQolLAKqp_7U3r1GUD3... New Chrome available: Naomi Question 26 of 39 (4 points) | Question Attempt: 1 of Unlimited Give the IUPAC name. 2,3-dimethylhexane Part: 1/2 Part 2 of 2 Draw the skeletal structure of a constitutional isomer of the alkane above that contains a different number of carbons in its longest chain. Skip Part Check Click and drag to start drawing a structure. 3 Finance headline Q Search mwa Harvard Intensifi... X Save For Later 00 dlo HB Submit Assignment 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility a 9:11 PM 4/22/2025

Predict the product of this organic reaction: + NH2 HO A P+ H2O Specifically, in the drawing area below draw the skeletal ("line") structure of P. If there is no reasonable possibility for P, check the No answer box under the drawing area. Click and drag to start drawing a structure. ✓

Answer 2

Question

Chapter 21.14, Problem 21.39P

(a)

Interpretation Introduction

Interpretation:

The accomplishment of the given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

The lithium aluminium hydride reduction of nitrile followed by hydrolysis gives primary amine.

(b)

Interpretation Introduction

Interpretation:

The accomplishment of given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

Grignard reagent is used to generate R− carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

(c)

Interpretation Introduction

Interpretation:

The accomplishment of given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

Grignard reagent is used to generate R− carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

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Answer 3

Question

Chapter 21.14, Problem 21.39P

(a)

Interpretation Introduction

Interpretation:

The accomplishment of the given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

The lithium aluminium hydride reduction of nitrile followed by hydrolysis gives primary amine.

(b)

Interpretation Introduction

Interpretation:

The accomplishment of given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

Grignard reagent is used to generate R− carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

(c)

Interpretation Introduction

Interpretation:

The accomplishment of given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

Grignard reagent is used to generate R− carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

Expert Solution & Answer

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Answer 4

Question

Chapter 21.14, Problem 21.39P

(a)

Interpretation Introduction

Interpretation:

The accomplishment of the given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

The lithium aluminium hydride reduction of nitrile followed by hydrolysis gives primary amine.

(b)

Interpretation Introduction

Interpretation:

The accomplishment of given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

Grignard reagent is used to generate R− carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

(c)

Interpretation Introduction

Interpretation:

The accomplishment of given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

Grignard reagent is used to generate R− carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

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Answer 5

Chapter 21.14, Problem 21.39P

(a)

Interpretation Introduction

Interpretation:

The accomplishment of the given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

The lithium aluminium hydride reduction of nitrile followed by hydrolysis gives primary amine.

(b)

Interpretation Introduction

Interpretation:

The accomplishment of given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

Grignard reagent is used to generate R− carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

(c)

Interpretation Introduction

Interpretation:

The accomplishment of given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

Grignard reagent is used to generate R− carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

Answer 6

Chapter 21.14, Problem 21.39P

(a)

Interpretation Introduction

Interpretation:

The accomplishment of the given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

The lithium aluminium hydride reduction of nitrile followed by hydrolysis gives primary amine.

Answer 7

Chapter 21.14, Problem 21.39P

(a)

Interpretation Introduction

Interpretation:

The accomplishment of the given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

The lithium aluminium hydride reduction of nitrile followed by hydrolysis gives primary amine.

Answer 8

(b)

Interpretation Introduction

Interpretation:

The accomplishment of given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

Grignard reagent is used to generate R− carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

Answer 9

(b)

Interpretation Introduction

Interpretation:

The accomplishment of given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

Grignard reagent is used to generate R− carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

Answer 10

(c)

Interpretation Introduction

Interpretation:

The accomplishment of given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

Grignard reagent is used to generate R− carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

Answer 11

(c)

Interpretation Introduction

Interpretation:

The accomplishment of given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

Grignard reagent is used to generate R− carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

Answer 12

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Answer 13

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Answer 14

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Answer 15

Ch. 21.2F - Name the following carboxylic acid derivatives,...Ch. 21.4A - Prob. 21.2P Ch. 21.4A - Prob. 21.3P Ch. 21.4A - Prob. 21.4P Ch. 21.5C - Prob. 21.7P Ch. 21.6 - When ethyl 4-hydroxybutyrate is heated in the...Ch. 21.6 - Propose a mechanism for the following ring-opening...Ch. 21.6 - Prob. 21.15P Ch. 21.7B - Prob. 21.16P Ch. 21.7C - Prob. 21.19P

The accomplishment of the given transformation by the use of nitrile as an intermediate is to be shown. Concept introduction: The lithium aluminium hydride reduction of nitrile followed by hydrolysis gives primary amine .

Solution Summary: The author illustrates the transformation of 1-hexanol by the use of nitrile as an intermediate. Grignard reagent is used to generate R- carbanion which

Concept explainers

Interpretation:

The accomplishment of the given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

The lithium aluminium hydride reduction of nitrile followed by hydrolysis gives primary amine.

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Chapter 21 Solutions

The accomplishment of the given transformation by the use of nitrile as an intermediate is to be shown. Concept introduction: The lithium aluminium hydride reduction of nitrile followed by hydrolysis gives primary amine .

Solution Summary: The author illustrates the transformation of 1-hexanol by the use of nitrile as an intermediate. Grignard reagent is used to generate R- carbanion which

Concept explainers

Interpretation: The accomplishment of the given transformation by the use of nitrile as an intermediate is to be shown. Concept introduction: The lithium aluminium hydride reduction of nitrile followed by hydrolysis gives primary amine.

Want to see the full answer?

Chapter 21 Solutions

Interpretation:

The accomplishment of the given transformation by the use of nitrile as an intermediate is to be shown.

Concept introduction:

The lithium aluminium hydride reduction of nitrile followed by hydrolysis gives primary amine.