Chap 14: ALDEHYDES AND KETONES

Slides:



Advertisements
Similar presentations
CHAPTER 14 CONCURRENT ENROLLMENT. NOMENCLATURE Carbonyl group Carbonyl group.
Advertisements

Chapter Sixteen Aldehydes and Ketones James E. Mayhugh Oklahoma City University  2007 Prentice Hall, Inc. Fundamentals of General, Organic, and Biological.
Organic Chemistry Aldehydes and Ketones
Chapter 14 Aldehydes and Ketones Spencer L. Seager Michael R. Slabaugh Jennifer P. Harris.
1 Chapter 14: Aldehydes and Ketones. 2 ALDEHYDES AND KETONES The carbonyl group: Aldehydes have at least one hydrogen attached to the carbonyl group.
1 Lecture 4: Aldehydes, Ketones, and Chiral Molecules 14.1 Aldehydes and Ketones Copyright © 2007 by Pearson Education, Inc. Publishing as Benjamin Cummings.
Aldehydes Ketones. Carbonyl group C = O Aldehydes Ketones Carboxylic acids Esters.
Chemistry: An Introduction to General, Organic, and Biological Chemistry, Twelfth Edition© 2015 Pearson Education, Inc Aldehydes and Ketones Vanilla.
Chapter 4 Ketones and Aldehydes. Chapter Carbonyl Structure Carbon is sp 2 hybridized. C=O bond is shorter, stronger, and more polar than C=C.
Chapter 14 Aldehydes, Ketones, and Chiral Molecules
Chapter 18 Ketones and Aldehydes Organic Chemistry, 6 th Edition L. G. Wade, Jr.
Prentice Hall;Copyright Reduction of Aldehydes and Ketones The reduction of a carbonyl group occurs with the addition of hydrogen across the.
Chapter 121 Carbonyl Compounds II: Chapter 12. Chapter 122 Contents of Chapter 12 Structure of Aldehydes and Ketones Naming Adehydes and Ketones Reactivity.
Chapter 15 Aldehydes and Ketones
Capsaicin. Aldehydes and ketones Carbonyl Compounds Contain the carbonyl group C=O Aldehydes: R may be hydrogen, usually a carbon containing group Ketones:
Aldehydes and ketones Chapter 15. The carbonyl group Aldehydes and ketones are among the first examples of compounds that possess a C-O double bond that.
Chapter 13 Aldehydes and Ketones Denniston Topping Caret 5th Edition
Bettelheim, Brown, Campbell and Farrell Chapter 17
Aldehydes and Ketones Chapter 23
ALDEHYDES & KETONES Melanin - a polymeric substance involving many interconnected cyclic ketone units that colors human hair & skin.
Aldehyde and ketones Lec.10. Introduction Aldehydes and ketones are characterized by the presence of the carbonyl group, perhaps the most important functional.
1 Principles and Applications of Inorganic, Organic, and Biological Chemistry Denniston, Topping, and Caret 4 th ed Chapter 14 Copyright © The McGraw-Hill.
1-1 Chemistry 121, Winter 2014, LA Tech Introduction to Organic Chemistry and Biochemistry Instructor Dr. Upali Siriwardane (Ph.D. Ohio State)
© 2003 Thomson Learning, Inc. All rights reserved General, Organic, and Biochemistry, 7e Bettelheim, Brown, and March.
Ch 17- Aldehydes and Ketones Homework: 17.10, 17.13, 17.17, 17.19, 17.28, 17.35, 17.40, 17.41, 17.49, 17.53,
Chapter 9 Aldehydes and Ketones Chemistry 20. Carbonyl group C = O Aldehydes Ketones Carboxylic acids Esters.
General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake 14.1 Aldehydes and Ketones Chapter 14 Aldehydes, Ketones, and Chiral Molecules.
Definition a CARBONYL GROUP is a functional group found in organic compounds composed of a Carbon atom double - bonded to an oxygen atom. ═ C O.
Chapter 16 Aldehydes and Ketones.
Chapter 14 Aldehydes and Ketones Spencer L. Seager Michael R. Slabaugh Jennifer P. Harris.
Aldehydes By: Nicole Murphy & Michaela Miller. General Structure What makes an aldehyde an aldehyde? A carbon double bonded to an oxygen molecule. This.
Structures of Aldehydes and Ketones Both aldehydes and ketones contain a carbonyl group Aldehydes have at least one H attached, while ketones have two.
Chapter 17: Aldehydes and Ketones -C-H = = O O -C- = = O O < Aldehydes. Cinnamaldehyde < Ketones. Acetone.
Chem. 108 Aldehydes and Ketones Chapter 9.
Chapter 11 Outline 11.1 Alcohols, Ethers, and Related Compounds
Chapter 9 Aldehydes and Ketones. Structure aldehyde The functional group of an aldehyde is a carbonyl group bonded to a hydrogen atom. In methanal, the.
Name as Substituent On a molecule with a higher priority functional group, C=O is oxo- and -CHO is formyl. Aldehyde priority is higher than ketone. 3-methyl-4-oxopentanal.
Prentice Hall Copyright 2007 Chapter Sixteen Aldehydes and Ketones James E. Mayhugh Oklahoma City University  2007 Prentice Hall, Inc. Fundamentals of.
Topic: Function Group #4-Ketones Do Now: In terms of IMF, explain the difference in boiling point.
1-1 Chemistry 121, Winter 2016, LA Tech Introduction to Organic Chemistry and Biochemistry Instructor Dr. Upali Siriwardane (Ph.D. Ohio State)
General, Organic and Biochemistry 7 th Edition ORGANIC CHEMISTRY Copyright  The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
1 Chapter 14 Aldehydes, Ketones, and Chiral Molecules 14.1 Aldehydes and Ketones Copyright © 2007 by Pearson Education, Inc. Publishing as Benjamin Cummings.
Chapter 2 Aldehydes and Ketones Introduction 1.Aldehydes 2.Nomenclature of Aldehydes 3.Physical Properties of Aldehydes 4.Chemical Properties of Aldehydes.
Aldehyde and Ketones R- CH = O R – C – R y O Session 37.
Lecture 11 Monday 2/8/17.
Sample Problem 14.1 Identifying Aldehydes and Ketones
Chapter 14 Ketones, and Chiral Molecules
Ketones and Aldehydes.
ORGANIC CHEMISTRY 13 Aldehydes and Ketones
Chapter 14 Aldehydes, Ketones, and Chiral Molecules
Lecture 9 Monday 2/6/17.
Aldehydes and Ketones.
16.5 Properties of Esters Ethyl acetate is the solvent in fingernail polish, plastics, and lacquers. Learning Goal Describe the boiling points and solubility.
1.5 ALDEHYDES AND KETONES.
Chapter 17 Aldehydes and Ketones
14.1 Aldehydes and Ketones Formaldehyde is the simplest aldehyde. It is a colorless gas with a pungent odor. An aqueous solution called formalin, which.
Chapter 14 Aldehydes, Ketones, and Chiral Molecules
Chem. 108 Aldehydes and Ketones Chapter 9.
Chapter 14 Aldehydes, Ketones, and Chiral Molecules
Fundamentals of Organic Chemistry
Fundamentals of Organic Chemistry
ALDEHYDES, KETONES AND CARBOXYLIC ACIDS
ALDEHYDES, KETONES AND CARBOXYLIC ACIDS
Fundamentals of Organic Chemistry
Chapter 14 Aldehydes, Ketones, and Chiral Molecules
Fundamentals of Organic Chemistry
ALDEHYDES AND KETONES.
Fundamentals of Organic Chemistry
Organic Chemistry CHEM 145
Presentation transcript:

Chap 14: ALDEHYDES AND KETONES The carbonyl group: Aldehydes have at least one hydrogen attached to the carbonyl group. Ketones have two carbons attached to the carbonyl group.

NAMING ALDEHYDES Examples: Find the longest carbon chain that contains the aldehyde group. Change ending of the root hydrocarbon name by dropping –e and adding –al. All other branches and groups are named and located using standard IUPAC system. Examples:

NAMING KETONES Examples: Find the longest chain that contains C=O. Using the root alkane name, drop the –e ending and change to –one. Number the longest carbon chain so the C=O group has the lowest number. Name and number other substituents as before. Examples:

PHYSICAL PROPERTIES The carbonyl group is moderately polar, but it doesn’t have any hydrogen atoms attached, so it cannot hydrogen bond between molecules.

PHYSICAL PROPERTIES, cont. Because of the polarity of the C=O group, these groups can interact, but the attraction is not as strong as hydrogen bonding. This makes the boiling point of aldehydes and ketones higher than alkanes, but lower than alcohols.

PHYSICAL PROPERTIES, cont. The C=O group can hydrogen bond with water molecules. This makes low molecular weight aldehydes and ketones water soluble (they have small hydrophobic sections). H O || R-C-R O

ALDEHYDE AND KETONE REACTIONS Recall the oxidation of alcohols to produce aldehydes and ketones:

REACTIONS, cont. The addition of H2 in the presence of catalysts.

Examples:

REACTIONS, cont. The addition of alcohols to aldehydes produces an unstable hemiacetal intermediate.

REACTIONS, cont. General formulas for: Hemiacetals Acetals

REACTIONS, cont. The addition of alcohol to ketones produces an unstable hemiketal intermediate.

REACTIONS, cont. General formula for: Hemiketal Ketal

REACTIONS, cont. Cyclical hemiacetals and hemiketals are more stable than open chains and are important in carbohydrate chemistry.

REACTIONS, cont. Acetals and ketals are stable, but may be converted back to aldehydes and ketones through acid catalyzed hydrolysis. Hydrolysis is the breakage of a bond by reaction with water. Acetal hydrolysis:

REACTIONS, cont. Ketal hydrolysis: Specific Example:

IMPORTANT ALDEHYDES AND KETONES Formaldehyde Gas at room temperature Formalin – 37% aqueous solution Sterilizer Embalming fluid Starting material for plastics such as Formica and Bakelite

IMPORTANT ALDEHYDES AND KETONES, cont. Acetone (propanone) Important organic solvent Used in such things as nail polish remover Miscible with water

IMPORTANT ALDEHYDES AND KETONES, cont. Progesterone and testosterone (female and male sex hormones) are ketones. Some aldehydes and ketones are very fragrant and are used in flavorings. Vanillin (vanilla) Cinnamaldehyde (cinnamon) Citral (citrus flavoring) Camphor (medicinal odor)