16.4 Naming Esters Esters such as ethyl butanoate provide the odor and flavor of many fruits, such as pineapples. Learning Goal Write the IUPAC and common.

Slides:



Advertisements
Similar presentations
AN ester is simply an oxygen bonded between two hydrocarbon atoms.
Advertisements

1 Carboxylic Acids, Esters, Amines and Amides Carboxylic Acids Properties of Carboxylic Acids Esters Esterification and Hydrolysis.
Goals for the day… Review practice Exam 3
Chemistry: An Introduction to General, Organic, and Biological Chemistry, Twelfth Edition© 2015 Pearson Education, Inc Esters By the 1800s, chemists.
Carboxylic Acids A carboxylic acid contains a a hydroxyl group (–OH) attached to a carboxyl group, which is a carbonyl group. © 2013 Pearson, Education.
Carboxylic Acids. A carboxylic acid contains a carboxyl group, which is a carbonyl group attach to a hydroxyl group. carbonyl group O  CH 3 — C—OH hydroxyl.
Acids and Esters. Organic Acids Also called carboxylic acids Functional group –Where in chain? Naming: Use HC root and add “oic acid” instead of ol Example:
Timberlake: General, Organic & Biological Chemistry Copyright ©2010 by Pearson Education, Inc. SAMPLE PROBLEM16.1 Naming Carboxylic Acids SOLUTION a. STEP.
Carboxylic Acids and Their Derivatives By: Dr. Shatha Alaqeel.
Higher Chemistry Unit 2 Multiple Choice Questions Section 6 Esters
Chapter 16 Carboxylic Acids and Esters
1 Lecture 6: Carboxylic Acids and Esters 16.1 Carboxylic Acids Copyright © 2007 by Pearson Education, Inc. Publishing as Benjamin Cummings.
26-3: Carboxylic Acids and Esters
Carboxylic Acids and Esters,
ORGANIC CHEMISTRY Any molecule that contains the element CARBON.
By: Adrianne Nelson.  They are an organic compound made by replacing the hydrogen of an acid by an alkyl or other organic group.  Esters are responsible.
1 © 2013 Pearson Education, Inc. Chapter 16, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake 16.1 Carboxylic Acids.
Unit 2 Esters. Go to question Which of the following compounds is an ester? a. b. c. d.
Esters Organic compound formed by the condensation reaction of a carboxylic acid and an alcohol. O O R-C-OH + R-OH R-C-O-R’ + H2O (ester)
ORGANIC ACID Carboxylic acid Alkanoic acid or. At the end of the lesson, pupils should be able to name, write and draw first four members of the alkanoic.
Carboxylic Acids Carboxyl group: -CO 2 H, -COOH Pure carboxylic acids form hydrogen bonded dimers very high boiling points (higher than alcohols) H-bond.
Carboxylic acids. Starter Which of the following formulae represent carboxylic acids? 1.CH 3 CH 2 CH(CH 3 )COOH 2.(CH 3 ) 2 CHCHO 3.CH 3 CH 2 OH 4.C 6.
Esters The smelly compounds. What are Esters?  A group of compounds that are responsible for some natural and synthetic flavours  They are often found.
Topic: Functional Group #7: Esters Do Now:. Esters General format R and R ‘ = hydrocarbon branches – Can be same or different Esters contain carbonyl.
Unit 2 Esters. Go to question Which of the following compounds is an ester? The structural formula of the ester formed between ethanol.
General, Organic, and Biological Chemistry Copyright © 2010 Pearson Education, Inc.1 Chapter 16 Carboxylic Acids and Esters 16.1 Carboxylic Acids.
Describe the hydrolysis of esters.
10.4 Carboxylic Acids Esters Esterfications. Carboxylic acids A carboxylic acid is an organic compound that contains the carboxyl group. Examples include.
Carboxylic acids, esters etc. Objectives To continue to learn about the structures and some of the uses of acids, ethers and esters.
Higher Chemistry Unit 2 Section 6 - Esters Multiple Choice Questions This is designed to be used by teachers to help students develop skills in answering.
PROBLEMS CH 14. Learning Check Identify the following compounds as either an aldehyde or ketone. A. CH 3 —CH 2 —CH 2 —COH B. CH 3 —CH 2 —CO—CH 2 —CH 2.
Carboxylic Acids and Their Derivatives By: Dr. Siham Lahsasni.
Formation of the ester ethyl propanoate from a carboxylic acid
Esters and Esterification. Esters produced by combining carboxylic acid and alcohol (esterification) Large chain esters account for flavor and odor.
Week 4 © Pearson Education Ltd 2009 This document may have been altered from the original Explain the water solubility of carboxylic acids. Describe the.
1.6 Carboxylic Acids and Esters
Organic Chemistry Functional Groups: - Aldehydes - Ketones
Carbonyl Compounds.
PROBLEMS CH 16. Learning Check Give the IUPAC and common names for the following. A. B. C.
Chemistry: An Introduction to General, Organic, and Biological Chemistry, Eleventh Edition Copyright © 2012 by Pearson Education, Inc. Chapter 14 Carboxylic.
Functional Groups: - Aldehydes - Ketones - Organic Acids - Esters.
+ +. After completing this topic you should be able to : State esters are formed by the condensation reaction between an alkanoic acid and an alcohol.
Organic Chemistry Alkanes and Alkenes. Pure Hydrocarbons Because the main use of hydrocarbons is as a fuel there is no point in going to the effort to.
Carboxylic Acids & Esters
Hydrocarbon Derivatives Aldehydes Ketones Carboxylic Acids Esters.
Carboxylic acids and Esters
Chapter 16 Carboxylic Acids
Sample Problem 16.1 Naming Carboxylic Acids
Chapter 1.6 Carboxylic Acids, Esters, and Fats
The Reaction between a Carboxylic acid and an Alcohol-Esterification
Carboxylic Acids, Esters, Amines and Amides
Esters By Cori and Shania.
Esters When alcohols are heated with carboxylic acids in the presence of concentrated sulfuric acid, they produce sweet smelling compounds called esters.
Carboxylic Acids.
Carboxylic Acids, Esters, Amines and Amides
Alkanoic acids and Esters
16.1 Carboxylic Acids A carboxylic acid contains a carboxyl group, which consists of a hydroxyl group to the carbon in a carbonyl group.
1.6 CARBOXYLIC ACIDS, ESTERS, AND FATS
Hydrocarbon Derivatives
PROBLEMS CH 16.
ORGANIC CHEMISTRY CHAPTER-1
Unit 2 Section 2.7 Esters.
CH3COOH Ethanoic acid Carboxylic Acids
CH3COOH Ethanoic acid Carboxylic Acids
Ester Functional Group Created by: Jenny Chase.
Pop-Quiz Sit down quietly and draw the following structures.
Esters and Esterification
Carboxylic Acids and Esters
Chapter 14 Aldehydes, Ketones, and Chiral Molecules
Presentation transcript:

16.4 Naming Esters Esters such as ethyl butanoate provide the odor and flavor of many fruits, such as pineapples. Learning Goal Write the IUPAC and common names for esters; draw condensed and line-angle structural formulas.

Naming Esters The name of an ester consists of two words: 1. The first word indicates the alkyl part from the alcohol. 2. The second word is the carboxylate name of the carboxylic acid.

Naming Esters Esters have IUPAC and common names:

Guide to Naming Esters

Naming Esters What is the IUPAC name of the following ester? STEP 1 Write the name for the carbon chain from an alcohol as an alkyl group ethyl ANALYZE Given Need THE ester IUPAC and common name PROBLEM

Naming Esters What is the IUPAC name of the following ester? STEP 2 Change the ic acid of the acid name to ate. ethyl propanoate ethyl propionate

Study Check Give the IUPAC and common names for the following compound, responsible for the flavor and odor of pears:

Solution Give the IUPAC and common names for the following compound, responsible for the flavor and odor of pears: STEP 1 Write the name for the carbon chain from an alcohol as an alkyl group. propyl ANALYZE Given Need THE ester IUPAC and common name PROBLEM

Solution Give the IUPAC and common names for the following compound, responsible for the flavor and odor of pears: STEP 2 Change the ic acid of the acid name to ate. propyl ethanoate propyl acetate

Esters in Fruits Many of the fragrances of perfumes and flowers and the flavors of fruits are due to esters. Small esters are volatile, so we can smell them, and they are soluble in water, so we can taste them. The odor of grapes is due to ethyl heptanoate.

Esters in Fruits and Flavoring

Study Check Draw the condensed structural formulas for each of the following compounds: A. propyl pentanoate B. ethyl propionate

Solution Draw the condensed structural formulas for each of the following compounds: A. propyl pentanoate B. ethyl propionate