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Chapter 17, Problem 81P

(a)

Interpretation Introduction

Interpretation: It should be indicated that how the given compound prepared from its given starting material.

Concept introduction: When an acyl group is attached to hydrogen then the compound is an aldehyde. When the acyl group is attached to an (R) group then the compound is a ketone. Both aldehydes and ketones undergo nucleophilic addition reaction.

Aldehydes react with Griganrds reagent to form secondary alcohols while ketones form tertiary alcohol. Aldehydes and ketones can be reduced in the presence of reagent NaBH4 and can be oxidized in the presence of NaOCl/CH3COOH.

(b)

Interpretation Introduction

Interpretation: It should be indicated that how the given compound prepared from its given starting material.

Concept introduction: When an acyl group is attached to hydrogen then the compound is an aldehyde. When the acyl group is attached to an (R) group then the compound is a ketone. Both aldehydes and ketones undergo nucleophilic addition reaction.

Aldehydes react with Griganrds reagent to form secondary alcohols while ketones form tertiary alcohol. Aldehydes and ketones can be reduced in the presence of reagent NaBH4 and can be oxidized in the presence of NaOCl/CH3COOH.

(c)

Interpretation Introduction

Interpretation: It should be indicated that how the given compound prepared from its given starting material.

Concept introduction: When an acyl group is attached to hydrogen then the compound is an aldehyde. When the acyl group is attached to an (R) group then the compound is a ketone. Both aldehydes and ketones undergo nucleophilic addition reaction.

Aldehydes react with Griganrds reagent to form secondary alcohols while ketones form tertiary alcohol. Aldehydes and ketones can be reduced in the presence of reagent NaBH4 and can be oxidized in the presence of NaOCl/CH3COOH.

(d)

Interpretation Introduction

Interpretation: It should be indicated that how the given compound prepared from its given starting material.

Concept introduction: When an acyl group is attached to hydrogen then the compound is an aldehyde. When the acyl group is attached to an (R) group then the compound is a ketone. Both aldehydes and ketones undergo nucleophilic addition reaction.

Aldehydes react with Griganrds reagent to form secondary alcohols while ketones form tertiary alcohol. Aldehydes and ketones can be reduced in the presence of reagent NaBH4 and can be oxidized in the presence of NaOCl/CH3COOH.

(e)

Interpretation Introduction

Interpretation: It should be indicated that how the given compound prepared from its given starting material.

Concept introduction: When an acyl group is attached to hydrogen then the compound is an aldehyde. When the acyl group is attached to an (R) group then the compound is a ketone. Both aldehydes and ketones undergo nucleophilic addition reaction.

Aldehydes react with Griganrds reagent to form secondary alcohols while ketones form tertiary alcohol. Aldehydes and ketones can be reduced in the presence of reagent NaBH4 and can be oxidized in the presence of NaOCl/CH3COOH.

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Chapter 17 Solutions

Organic Chemistry; Modified MasteringChemistry with Pearson eText -- ValuePack Access Card; Study Guide and Student Solutions Manual for Organic Chemistry, Books a la Carte Edition (7th Edition)

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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