aldehydes & ketones dr. michael p. gillespie. introduction the aldehydes and ketones are...

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Aldehydes & Ketones Dr. Michael P. Gillespie

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Page 1: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Aldehydes & Ketones

Dr. Michael P. Gillespie

Page 2: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Introduction

• The aldehydes and ketones are characterized by the presence of the carbonyl group.

• The carbonyl group is a functional group made up of a carbon atom bonded to an oxygen atom by a double bond.

• Carbonyl compounds are those that contain a carbonyl group.

• Aldehydes, ketones, carboxylic acids, and amides all are carbonyl compounds.

2Dr. Michael P. Gillespie

Page 3: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Carbonyl Group

• The carbonyl group is a functional group made up of a carbon atom bonded to an oxygen atom by a double bond.

• Carbonyl groups are polar.

Dr. Michael P. Gillespie 3

Page 4: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Structure and Physical Properties Aldehydes

• In aldehydes the carbonyl group is attached to at least one hydrogen; the second group may be attached to another hydrogen or a carbon atom.

• Aldehydes are polar due to the polar nature of the carbonyl group.

Dr. Michael P. Gillespie 4

Page 5: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Structure and Physical Properties Aldehydes

• Aldehydes have higher boiling points than comparable hydrocarbons, but lower boiling points than comparable alcohols.

• Small aldehydes are reasonably soluble in water.

• Large aldehydes are less polar and dissolve more readily in nonpolar organic solvents.

Dr. Michael P. Gillespie 5

Page 6: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Aldehydes

Dr. Michael P. Gillespie 6

Page 7: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Structure and Physical Properties Ketones

• In ketones, the carbonyl group is attached to two carbon containing groups.

• Ketones are polar due to the polar nature of the carbonyl group.

Dr. Michael P. Gillespie 7

Page 8: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Structure and Physical Properties Ketones

• Ketones have higher boiling points than comparable hydrocarbons, but lower boiling points than comparable alcohols.

• Small ketones are reasonably soluble in water.

• Large ketones are less polar and dissolve more readily in nonpolar organic solvents.

Dr. Michael P. Gillespie 8

Page 9: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Ketones

Dr. Michael P. Gillespie 9

Page 10: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Important Aldehydes & Ketones

• Many members of the aldehyde and ketone family are important as food and fragrance chemicals, medicinals, and agriculture chemicals.

• Methanal (formaldehyde) is used to preserve tissue.

• Ethanal causes the symptoms of hangover.

• Ethanal is oxidized to produce acetic acid.

• Propanone is a useful organic solvent.

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Page 11: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Preparation of Aldehydes & Ketones

• Aldehydes and ketones are prepared by the oxidation of alcohols.

Dr. Michael P. Gillespie 11

Page 12: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Oxidation Reactions

• Oxidation of a primary alcohol yields an aldehyde.

• Oxidation of a secondary alcohol yields a ketone.

• Tertiary alcohols do not react under these conditions.

Dr. Michael P. Gillespie 12

Page 13: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Oxidation Reactions

• Aldehydes can be further oxidized to carboxylic acids. Ketones do not undergo further oxidation.

• Tollen’s test and Benedict’s test utilize this principle to distinguish between the two.

Dr. Michael P. Gillespie 13

Page 14: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Reduction Reactions

• Aldehydes and Ketones are readily reduced to alcohols by hydrogenation.

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Page 15: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Addition Reactions

• The most common reaction is addition across the double bond of the carbonyl group.

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Page 16: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Aldol Condensation

• Aldol condensation is a reaction in which aldehydes and ketones form larger molecules.

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Page 17: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Alcohol Abuse

• According to the Centers for Disease Control and Prevention, more than 75,000 Americans die each year from alcohol abuse.• 35,000 die of cirrhosis of the liver.• Nearly 41,000 die of alcohol related

automobile accidents.• An estimated 1400 college-age students

die each year of alcohol related causes.

• Alcohol abuse is the third leading cause of preventable death in the United States.

Dr. Michael P. Gillespie 17

Page 18: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Antabuse

• The drug tetraethylthiuram disulfide (disulfiram) is used to treat alcohol abuse. It is otherwise known as antabuse.

• People who take Antabuse become violently ill after consuming any alcoholic beverage.

• The compound inhibits one of the enzymes in the pathway to oxidize alcohols.

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Page 19: Aldehydes & Ketones Dr. Michael P. Gillespie. Introduction The aldehydes and ketones are characterized by the presence of the carbonyl group. The carbonyl

Antabuse

• The inhibition occurs within 1-2 hours after consuming the drug and lasts up to 14 days.

• When a person who has taken Antabuse drinks an alcoholic beverage, the levels of acetylaldehyde reach levels that are 5 – 10 times higher than would normally occur after a drink.

• Symptoms of a severe hangover occur within minutes and may last for hours.

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