Organic Chemistry (Looseleaf) - With Access
Organic Chemistry (Looseleaf) - With Access
7th Edition
ISBN: 9780134325774
Author: Bruice
Publisher: PEARSON
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Chapter 17, Problem 60P

(a)

Interpretation Introduction

Interpretation:

From the given reaction it should be showed that how the product is prepared from the starting material.

Concept Introduction:

Oxidation: If electrons are moved from a species during a chemical reaction. The species whose electrons are removed is said to be oxidized.

Generally, oxidation of aldehyde or ketones gives alcohol which on further oxidation results in formation of acids.

(b)

Interpretation Introduction

Interpretation:

From the given reaction it should be showed that how the product is prepared from the starting material.

Concept Introduction:

Reduction: If electrons are gained to a species during a chemical reaction. The species which gets electrons are said to be reduced.

Generally, reduction of primary alcohol results to give aldehyde.

Aldehyde (except formaldehyde) in presence of Grignard Reagent results in formation of secondary alcohol.

Oxidation: If electrons are moved from a species during a chemical reaction. The species whose electrons are removed is said to be oxidized.

Generally, oxidation of primary alcohol forms aldehyde and secondary alcohol forms ketone.

(c)

Interpretation Introduction

Interpretation:

From the given reaction it should be showed that how the product prepared from the starting material.

Concept introduction:

Reduction: If electrons are gained to a species during a chemical reaction. The species which gets electrons are said to be reduced.

Reaction for aldehydes and ketones in presence of primary amine is as follows,

The carbonyl group of a carboxylic acid or carboxylic acid derivative gets converted into imine in presence of primary amine which is depicted as follows,

Organic Chemistry (Looseleaf) - With Access, Chapter 17, Problem 60P

Oxidation: If electrons are moved from a species during a chemical reaction. The species whose electrons are removed is said to be oxidized.

Generally, oxidation of primary alcohol forms aldehyde and secondary alcohol forms ketone.

(d)

Interpretation Introduction

Interpretation:

From the given reaction it should be showed that how the product is prepared from the starting material.

Concept introduction:

Reduction: If electrons are gained to a species during a chemical reaction. The species which gets electrons are said to be reduced.

Oxidation: If electrons are moved from a species during a chemical reaction. The species whose electrons are removed is said to be oxidized.

Generally, oxidation of primary alcohol forms aldehyde and secondary alcohol forms ketone.

(e)

Interpretation Introduction

Interpretation:

From the given reaction it should be showed that how the product is prepared from the starting material.

Concept introduction:

Reduction: If electrons are gained to a species during a chemical reaction. The species which gets electrons are said to be reduced.

Oxidation: If electrons are moved from a species during a chemical reaction. The species whose electrons are removed is said to be oxidized.

Generally, oxidation of primary alcohol forms aldehyde and secondary alcohol forms ketone.

Ketone in presence of Grignard Reagent results to form tertiary alcohol.

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Chapter 17 Solutions

Organic Chemistry (Looseleaf) - With Access

Ch. 17.4 - Show how the following compounds can be...Ch. 17.5 - Prob. 13PCh. 17.5 - Prob. 14PCh. 17.6 - In the mechanism for cyanohydrin formation, why is...Ch. 17.6 - Prob. 16PCh. 17.6 - Prob. 17PCh. 17.6 - Show two ways to convert an alkyl halide into a...Ch. 17.7 - Prob. 20PCh. 17.7 - Prob. 21PCh. 17.7 - Prob. 22PCh. 17.7 - Prob. 23PCh. 17.8 - Prob. 24PCh. 17.9 - What reducing agents should be used to obtain the...Ch. 17.9 - Prob. 26PCh. 17.9 - Prob. 27PCh. 17.10 - Prob. 28PCh. 17.10 - Prob. 29PCh. 17.10 - Prob. 30PCh. 17.10 - The pKa of protonated acetone is about 7.5. and...Ch. 17.10 - Prob. 32PCh. 17.10 - Prob. 33PCh. 17.10 - Prob. 34PCh. 17.10 - Excess ammonia must be used when a primary amine...Ch. 17.10 - The compounds commonly known as amino acids are...Ch. 17.11 - Hydration of an aldehyde is also catalyzed by...Ch. 17.11 - Which ketone forms the most hydrate in an aqueous...Ch. 17.11 - When trichloroacetaldehyde is dissolved in water,...Ch. 17.12 - Which of the following are a. hermiacetals? b....Ch. 17.12 - Prob. 41PCh. 17.12 - Explain why an acetal can be isolated but most...Ch. 17.13 - Prob. 43PCh. 17.13 - Prob. 44PCh. 17.13 - What products would be formed from the proceedings...Ch. 17.13 - a. In a six-step synthesis, what is the yield of...Ch. 17.13 - Show how each of the following compounds could be...Ch. 17.15 - Prob. 48PCh. 17.17 - Prob. 50PCh. 17.18 - Prob. 51PCh. 17.19 - Prob. 52PCh. 17 - Draw the structure for each of the following: a....Ch. 17 - Prob. 54PCh. 17 - Prob. 55PCh. 17 - a. Show the reagents required to form the primary...Ch. 17 - Prob. 57PCh. 17 - Using cyclohexanone as the starting material,...Ch. 17 - Prob. 59PCh. 17 - 60. Show how each of the following compounds could...Ch. 17 - Fill in the boxes:Ch. 17 - Prob. 62PCh. 17 - Identify A through O:Ch. 17 - Prob. 64PCh. 17 - Prob. 65PCh. 17 - Prob. 66PCh. 17 - How many signals would the product of the...Ch. 17 - Prob. 68PCh. 17 - Prob. 69PCh. 17 - Prob. 70PCh. 17 - Prob. 71PCh. 17 - Prob. 72PCh. 17 - Prob. 73PCh. 17 - Prob. 74PCh. 17 - Prob. 75PCh. 17 - Prob. 76PCh. 17 - Prob. 77PCh. 17 - A compound gives the following IR spectrum. Upon...Ch. 17 - a. Propose a mechanism for the following reaction:...Ch. 17 - Prob. 80PCh. 17 - Prob. 81PCh. 17 - Prob. 82PCh. 17 - Prob. 83PCh. 17 - Prob. 84PCh. 17 - In the presence of an acid catalyst, acetaldehyde...Ch. 17 - Prob. 86PCh. 17 - Prob. 87PCh. 17 - Prob. 88PCh. 17 - A compound reacts with methylmagnesium bromide...Ch. 17 - Show how each of the following compounds can be...Ch. 17 - Prob. 91PCh. 17 - Prob. 92PCh. 17 - The pKa values of the carboxylic acid groups of...Ch. 17 - The Baylis-Hillman reaction is a DABCO...Ch. 17 - Prob. 95PCh. 17 - Prob. 96P
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