Organic Chemistry (9th Edition)
Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
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Chapter 10.11B, Problem 10.25P

(a)

Interpretation Introduction

To determine: The product from the reaction of LiAlH4 with the given compound.

Interpretation: The product from the reaction of LiAlH4 with the given compound is to be stated.

Concept introduction: Lithium aluminum hydride LiAlH4 is much stronger reducing reagent than sodium borohydride NaBH4. It easily reduces less reactive carbonyl groups like carboxylic acids and esters and also reduces ketones and aldehyde.

It reduces aldehyde, carboxylic acids and esters to primary alcohol, and ketones to secondary alcohol.

The reaction of LiAlH4 with aldehyde, carboxylic acids, esters and ketone is followed by the hydrolysis to give the product in the reaction.

(b)

Interpretation Introduction

To determine: The products from the reaction of LiAlH4 with the given compound.

Interpretation: The products from the reaction of LiAlH4 with the given compound are to be stated.

Concept introduction: Lithium aluminum hydride LiAlH4 is much stronger reducing reagent than sodium borohydride NaBH4. It easily reduces less reactive carbonyl groups like carboxylic acids and esters and also reduces ketones and aldehyde.

It reduces aldehyde, carboxylic acids and esters to primary alcohol, and ketones to secondary alcohol.

The reaction of LiAlH4 with aldehyde, carboxylic acids, esters and ketone is followed by the hydrolysis to give the product in the reaction.

(c)

Interpretation Introduction

To determine: The product from the reaction of LiAlH4 with the given compound.

Interpretation: The product from the reaction of LiAlH4 with the given compound is to be stated.

Concept introduction: Lithium aluminum hydride LiAlH4 is much stronger reducing reagent than sodium borohydride NaBH4. It easily reduces less reactive carbonyl groups like carboxylic acids and esters and also reduces ketones and aldehyde.

It reduces aldehyde, carboxylic acids and esters to primary alcohol, and ketones to secondary alcohol.

The reaction of LiAlH4 with aldehyde, carboxylic acids, esters and ketone is followed by the hydrolysis to give the product in the reaction.

(d)

Interpretation Introduction

To determine: The product from the reaction of LiAlH4 with the given compound.

Interpretation: The product from the reaction of LiAlH4 with the given compound is to be stated.

Concept introduction: Lithium aluminum hydride LiAlH4 is much stronger reducing reagent than sodium borohydride NaBH4. It easily reduces less reactive carbonyl groups like carboxylic acids and esters and also reduces ketones and aldehyde.

It reduces aldehyde, carboxylic acids and esters to primary alcohol, and ketones to secondary alcohol.

The reaction of LiAlH4 with aldehyde, carboxylic acids, esters and ketone is followed by the hydrolysis to give the product in the reaction.

(e)

Interpretation Introduction

To determine: The products from the reaction of LiAlH4 with the given compound.

Interpretation: The products from the reaction of LiAlH4 with the given compound are to be stated.

Concept introduction: Lithium aluminum hydride LiAlH4 is much stronger reducing reagent than sodium borohydride NaBH4. It easily reduces less reactive carbonyl groups like carboxylic acids and esters and also reduces ketones and aldehyde.

It reduces aldehyde, carboxylic acids and esters to primary alcohol, and ketones to secondary alcohol.

The reaction of LiAlH4 with aldehyde, carboxylic acids, esters and ketone is followed by the hydrolysis to give the product in the reaction.

(f)

Interpretation Introduction

To determine: The product from the reaction of LiAlH4 with the given compound.

Interpretation: The product from the reaction of LiAlH4 with the given compound is to be stated.

Concept introduction: Lithium aluminum hydride LiAlH4 is much stronger reducing reagent than sodium borohydride NaBH4. It easily reduces less reactive carbonyl groups like carboxylic acids and esters and also reduces ketones and aldehyde.

It reduces aldehyde, carboxylic acids and esters to primary alcohol, and ketones to secondary alcohol.

The reaction of LiAlH4 with aldehyde, carboxylic acids, esters and ketone is followed by the hydrolysis to give the product in the reaction.

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Chapter 10 Solutions

Organic Chemistry (9th Edition)

Ch. 10.8B - Prob. 10.11PCh. 10.8B - Prob. 10.12PCh. 10.9A - Prob. 10.13PCh. 10.9B - Prob. 10.14PCh. 10.9C - Show how you would synthesize each tertiary...Ch. 10.9D - Prob. 10.16PCh. 10.9D - Show how you would add Grignard reagents to acid...Ch. 10.9D - A formate ester, such as ethyl formate, reacts...Ch. 10.9E - Prob. 10.19PCh. 10.9E - In Section9-7B, we saw how acetylide ions add to...Ch. 10.9F - Prob. 10.21PCh. 10.10A - Prob. 10.22PCh. 10.10B - Prob. 10.23PCh. 10.11B - Predict the products you would expect from the...Ch. 10.11B - Prob. 10.25PCh. 10.11B - Prob. 10.26PCh. 10.12 - Prob. 10.27PCh. 10.12 - Prob. 10.28PCh. 10.12 - Authentic skunk spray has become valuable for use...Ch. 10 - Give a systematic (IUPAC) name for each alcohol....Ch. 10 - Give systematic (IUPAC) names for the following...Ch. 10 - Draw the structures of the following compounds...Ch. 10 - Predict which member of each pair has the higher...Ch. 10 - Predict which member of each pair is more acidic,...Ch. 10 - Predict which member of each group is most soluble...Ch. 10 - Draw the organic products you would expect to...Ch. 10 - Prob. 10.37SPCh. 10 - Show how you would synthesize the following...Ch. 10 - Show how you would use Grignard syntheses to...Ch. 10 - Show how you would accomplish the following...Ch. 10 - Show how you would synthesize the following: a....Ch. 10 - Complete the following acid-base reactions. In...Ch. 10 - Prob. 10.43SPCh. 10 - Prob. 10.44SPCh. 10 - Geminal diols, or 1,1-diols, are usually unstable,...Ch. 10 - Vinyl alcohols are generally unstable, quickly...Ch. 10 - Compound A (C7H11Br) is treated with magnesium in...Ch. 10 - Prob. 10.48SPCh. 10 - Prob. 10.49SPCh. 10 - Prob. 10.50SPCh. 10 - Prob. 10.51SPCh. 10 - Prob. 10.52SPCh. 10 - Prob. 10.53SPCh. 10 - Prob. 10.54SPCh. 10 - Prob. 10.55SPCh. 10 - Prob. 10.56SPCh. 10 - Show how this 1 alcohol can be made from the...Ch. 10 - Prob. 10.58SPCh. 10 - Prob. 10.59SPCh. 10 - Prob. 10.60SP
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