Making Soap “Soaponification”

Slides:



Advertisements
Similar presentations
CHAPTER 15 CONCURRENT ENROLLMENT. CARBOXYLIC ACID CCCCarboxylic acid or carboxyl group - is an organic compound that contains the following functional.
Advertisements

N ATURE ’ S C HEMISTRY Soaps, Detergents and Emulsions.
International Comenius Project at GJAR From matter of the heart To the heart of matter.
Aim: Why do organic reactions occur more slowly than inorganic reactions? Combustion- Hydrocarbons (HC’s) will burn with sufficient amount of oxygen to.
Lipids Oil, greasy organic substances found in living organisms Insoluble in water (because water is very polar) Soluble in organic solvents (benzene,
Lipids, Proteins, and Carbohydrates
1 18.3Waxes, Fats, and Oils 18.4Chemical Properties of Triacylglycerols Chapter 18 Lipids.
Determination of Saponification Number
15.4 Chemical Properties of Triacylglycerols
Esters of Carboxylic Acids 17.5 Naming Esters 17.6 Properties of Esters Chapter 17 Carboxylic Acids And Esters.
1 Lipids Types of Lipids Fatty Acids Fats, and Oils Chemical Properties of Triglycerides.
1 Chapter 6 Lipids 6.4 Waxes, Fats, and Oils Copyright © 2005 by Pearson Education, Inc. Publishing as Benjamin Cummings.
Chemistry of Soap Getting Down and Dirty. Differences in Electronegativity If the difference in electronegativity is ___________ between two elements.
 Many people are lactose intolerant. These people cannot digest milk products because their bodies do not produce enough of the enzyme lactase to digest.
BASES Arrhenius defined a base as any compound that dissolves in water and yields a hydroxide ion.
IMPORTANT FUNCTIONS OF LIPIDS
Chapter 15: Carboxylic Acids and Esters
Saponification General reaction Fat + Base  Soap + glycerine Base = chemical that contains OH at the end Creating soap from fats or oils. Soaps are usually.
Organic Chemistry. Organic Compounds Def: Cmpds that are contain mostly carbon and hydrogen (millions) Ex) plastics, foods, fabrics Inorganic cmpds –
Organic Reactions Page 696 in Text Page 10:41 in Regents Review Book.
Reactions of Carboxylic Acids, Carboxylate Salts, and Carboxylate Esters Susan F. Hornbuckle Associate Professor of Chemistry Clayton State University.
Carboxylic Acids Carboxylic acids contain a carboxyl group: O CH 3 C-O-H ORCH 3 CO 2 H Carboxyl group.
Properties and reactions of Esters
Lipids General Characteristics Classification Biological function
Chapter 15 Carboxylic Acids and Esters Spencer L. Seager Michael R. Slabaugh Jennifer P. Harris.
Lipids-I BCH 302 [practical].
Understanding Soap. When was soap first used?  Soaps have been excavated in clay cylinders that date back to 2800 B.C.  An ancient Egyptian scroll dated.
What is Soap. water oil soap molecule If oil is added to water, the two liquids do not mix. Because of this, grease stains can be difficult to remove.
After completing this lesson you should be able to : Esters can be hydrolysed to produce the parent carboxylic acid and parent alcohol. Given the name.
CH 8: Lipids.
Chapter 15 Carboxylic Acids and Esters Spencer L. Seager Michael R. Slabaugh Jennifer P. Harris.
ESTERS. What is an ester? Responsible for tastes and odours. Contain the ester linkage Made from an alcohol and a carboxylic acid. Since the C=O group.
Glycerol is one of the building blocks in lipids. It is a 3C alcohol.
1 Chapter 15: Carboxylic Acids and Esters. 2 CARBOXYLIC ACIDS The functional group of carboxylic acids is the carboxyl group. Many carboxylic acids have.
Chemistry: An Introduction to General, Organic, and Biological Chemistry, Eleventh Edition Copyright © 2012 by Pearson Education, Inc. Chapter 14 Carboxylic.
Carboxylic Acids carboxyl group The functional group of a carboxylic acid is a carboxyl group, which can be represented in any one of three ways.
LIPIDS.
Organic Chemistry The study of carbon and carbon-containing compounds.
Naming esters Basically, an organic group is substituted in for the H in a carboxylic acids The first part of the name comes from the alcohol. Second part.
Do Now: Review your notes about substitution and addition and reactions and then complete this chart: Name Molecular formula Structural formula 2,3-dichloropentane.
17.4 Chemical Properties of Triacylglycerols
Why does fruit smell so good?
Chapter 15: Carboxylic Acids and Esters
Long term energy storage
Organic Reactions - The Saga Continues
PART III: ORGANIC REACTIONS
Soaps, Detergents and Emulsions
16.5 Properties of Esters Ethyl acetate is the solvent in fingernail polish, plastics, and lacquers. Learning Goal Describe the boiling points and solubility.
Chapter 16 Carboxylic Acids and Esters
Aim: Why do organic reactions occur more slowly than inorganic reactions? Combustion- Hydrocarbons (HC’s) will burn with sufficient amount of oxygen to.
Long term energy storage
Oils and Fats Major Component (%95-99) Triglycerides
Lipids Packet #10 Chapter #5.
Lubrication Prepared By Dr. Biswajit Saha.
Lipids.
Chemical Properties of Triglycerides
Chapter 17 Naturally Occurring Oxygen-Containing Compounds
Experiment one Measuring the saponification value of castor oil
Types of Organic Reactions
The study of carbon and carbon-containing compounds
7.7 Making Soaps Triglycerides
BASES Arrhenius defined a base as any compound that dissolves in water and yields a hydroxide ion.
Chapter 16 Carboxylic Acids and Esters
Chemical Properties of Triglycerides
Lipids Made up of C, H and O Can exist as fats, oils and waxes
ESTERS.
Long term energy storage
ESTERS.
Packet #10 Campbell—Chapter #5
Chemistry/Physical Setting
Presentation transcript:

Making Soap “Soaponification” Saponification Making Soap “Soaponification”

Saponification Reaction: Fat + Lye  Soap + Glycerol

Lye - Caustic solution made from ashes. Soda Lye = NaOH Potash Lye = KOH Combining potash K2CO3 with slaked lime Ca(OH)2 yields KOH and CaCO3 NaOH obtained from reacting sodium compounds.

O H C17H35-C-O-C-H + NaOH  O H Fat Lye (Triglyceride)

O H C17H35-C-ONa H-C-OH O C17H35-C-ONa + H-C-OH H Soap! Glycerol

How does it happen?? O Break the ester linkages C – O- by hydrolyzing the bonds between the carbon backbone and the fatty acid chains. (Reversal of esterification reaction) Form the sodium salt of a fatty acid (soap) and a trihydroxy alcohol (glycerol).

The Chemistry http://en.wikipedia.org/wiki/Saponification

Organic Reaction: Slow! Must break covalent bonds. Refluxing: Technique which allows a volatile solvent to boil, condense and return to the reaction vessel. It helps to maintain a fairly constant temperature throughout the reaction period.

BUMPING!!! When superheated liquids above their boiling point suddenly boil. Large bubbles cause liquid to shoot out of container. Add boiling chips to prevent bumping.

Strange but true… Fat in cadavers: saponifies if conditions are right. Alkalai environment, moist, minimal oxygen. Adipocere or grave wax is formed.