PURPOSE: To synthesize soap from fat and lye. To observe the physical and chemical properties of soap.

Similar documents
Preparation and Comparison of Soaps Minneapolis Community and Tech. College C1152 Principles of Chemistry II v.5.10

H O. rapidly reduces. They dissolve. because they can hydrogen bond to the water molecules.

Experiment 12 Lipids. Structures of Common Fatty Acids Name Number of carbons

Introduction to the Study of Lipids

Esters. What intermolecular forces do you think esters have? δ + CH 3

EXPERIMENT 9 LIPIDS: DETERMINATION OF FAT IN FRENCH FRIES. a fat molecule. Materials Needed

EXPERIMENT 9 LIPIDS: DETERMINATION OF FAT IN FRENCH FRIES. a fat molecule. Materials Needed

EXERCISE 3 Carbon Compounds

The four levels of protein structure are: primary structure, secondary structure, tertiary structure, and quaternary structure.

9. Determine the mass of the fat you removed from the milk and record in the table. Calculation:

Organic Molecule Composition of Milk: Lab Investigation

ANIMALS OILS AND FATS CHAPTER 2 PREPARATION AND SAPONIFICATION OF SPERMACETI 1. PREPARATION OF SPERMACETI

Carboxylic Acid Derivatives

Lecture 30: Soaps and Detergents

12BL Experiment 2: Extraction & Saponification of Trimyristin from Nutmeg

Review of Research into Fat, Oil and Grease (FOG) Deposits in Collection Systems. Casey R. Furlong, P.E. Environmental Specialist InSinkErator

15.1 Lipids 15.2 Fatty Acids. Copyright 2009 by Pearson Education, Inc.

CH 3. Lipids CHAPTER SUMMARY

Physical properties: C L = L. Cl, NH 2, OCH 3, OH, OCR O O O NH 2 CH 3 N(CH 3 ) 2. Sol. in H 2 O

Downloaded from

Carboxylic Acids and Esters

Chem 263 Dec 1, 2016

Characterization of Fatty Acid Used In Soap Manufacturing In Nigeria: Laundry, Toilet, Medicated and Antiseptic Soap

CHAPTER4 ANSWERS. Multiple Choice Questions. Short Answer Questions. 1. (b) 2. (d) 3. (a) 4. (c) 5. (c) 6. (b) 7. (a) 8. (b)

Carboxylic Acids, Esters and Acyl Chlorides

St Andrew s and St Bride s High Higher Chemistry and Emulsions. fats and oils by sodium or potassium hydroxide by boiling under reflux conditions:

Factors to Consider in the Study of Biomolecules

OCR (A) Biology A-level

EXPERIMENT 8 (Organic Chemistry II) Carboxylic Acids Reactions and Derivatives

Calderglen High School CfE Higher Chemistry. Nature s Chemistry. Soaps, Detergents and Emulsions

THERMALLY OXIDIZED SOYA BEAN OIL interacted with MONO- and DIGLYCERIDES of FATTY ACIDS

3.1.3 Lipids. Source: AQA Spec

What is the intermolecular force present in these molecules? A) London B) dipole-dipole C) hydrogen bonding D) ion-dipole E) None. D.

They are substances that are soluble in lipid or derived from the lipids by hydrolysis; for examples, cholesterol and fat soluble vitamins.

Interesterification. 4.1 Introduction. Chapter 4. Efforts have been made to improve the low-temperature properties by blending the

2. Now that you have made your hypothesis, you will begin. must perform at least 3 trials. Pleasee complete

Properties of Alcohols and Phenols Experiment #3

3150:112 SAMPLE TEST 2. Print out a copy Answer the questions on your own. Check the answers at GOBC Ans.pdf. Good Luck!

Name the ester produced when methanol and pentanoic acid react. methyl pentanoate. Name the type of reaction used to make an ester

THERMALLY OXIDIZED SOYA BEAN OIL

Important reactions of lipids

Chemistry Chapter 21

Figure 2. Figure 1. Name: Bio AP Lab Organic Molecules

For example, monosaccharides such as glucose are polar and soluble in water, whereas lipids are nonpolar and insoluble in water.

Alcohol aldehydes cetones and carboxylic acids

A carboxylic acid is an organic compound that contains a carboxyl group, COOH

FATS & OILS GLOSSARY

SYNTHESIS OF QUATERNARY AMMONIUM COMPOUNDS FROM NATURAL MATERIALS

Carboxylic Acids and Their Derivatives. Chapter 17. Carboxylic Acids and Their Derivatives

BIOB111_CHBIO - Tutorial activity for Session 12

Milk Experiment Background and Procedure

Carboxylic Acids and their Derivatives I

Save My Exams! The Home of Revision For more awesome GCSE and A level resources, visit us at Lipids.

(Writing model for laboratory note book)

Biodiesel Fundamentals for High School Chemistry Classes. Laboratory 3: Determination of the Acid Number of Vegetable Oils by Titration

Chemistry 1506: Allied Health Chemistry 2. Section 8: Lipids. Biochemical Esters and Hydrocarbons. Outline

Carboxylic Acids and Esters

RICINOLEATE UPON BACTERIA

Pectins. Residue Monograph prepared by the meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 82 nd meeting 2016

CHAPTER 28 LIPIDS SOLUTIONS TO REVIEW QUESTIONS

O C C C. Human cannot synthesize ten of the twenty common amino acids found in protein; these essential amino acids must be supplied in the diet.

Calderglen High School CfE Higher Chemistry. Nature s Chemistry Esters, Fats and Oils. Page 1 of 11

2.1.1 Biological Molecules

of Life Chemical Aspects OBJ ECTIVESshould be able to: ENCOUNTERS WITH LIFE H" ~ ~O N-C-C H R OH After completing this exercise, the student

Dr. Nafith Abu Tarboush

10 th International Junior Science Olympiad, Pune, India. Experimental Tasks. Examination Rules: Task: C Tomato (6 marks for this task)

H N H H C R H R' O C O C C R'' 2H 2 O H N

Chemistry 506: Allied Health Chemistry 2. Chapter 17: Lipids. Biochemical Esters and Hydrocarbons

6/9/2015. Unit 15: Organic Chemistry Lesson 15.2: Substituted Hydrocarbons & Functional Groups

Properties of Alcohols and Phenols Experiment #3

CHAPTER 28 LIPIDS SOLUTIONS TO REVIEW QUESTIONS

EXPERIMENT 6 Properties of Carbohydrates: Solubility, Reactivity, and Specific Rotation

Chapter 2 Part 3: Organic and Inorganic Compounds

INTERMEDIATE 1 1 Food and Diet. These elements are present in compounds - not as free elements.

CfE Higher Chemistry. Unit 2: Natures Chemistry. Esters, Fats and Oils, Soaps

12AL Experiment 8 (3 days): Synthesis of Isopentyl Acetate (aka: Banana Oil)

Lutein Esters from Tagetes Erecta

Functions of Lipids. - Storage Fats are long term energy (9 kcal/g) while carbohydrates are quick energy (4 kcal/g).

Chemistry in Everyday life

Experiment 9 Amino Acids and Proteins

LIPIDS II: TRIACYLGLYCEROLS:

Acid/Base chemistry. NESA Biochemistry Fall 2001 Review problems for the first exam. Complete the following sentences

Lipids and Classification:

Purity Tests for Modified Starches

THE ETHER-SOLUBLE SUBSTANCES OF CABBAGE LEAF CYTOPLASM. CL. FURTHER OBSERVATIONS ON DI- GLYCERIDEPHOSPHORIC ACID. IV. (Received August 29th, 1927.

MCQS ON LIPIDS. Dr. RUCHIKA YADU

Classification, functions and structure

Biology Chapter 2 Review

Chapter 20 Carboxylic Acids. Introduction

Biochemistry Worksheet

Chapter 20 Lipids. Organic and Biochem

Petrolatum. Stage 4, Revision 1. Petrolatum is a purified semi solid mixture of hydrocarbons obtained from petroleum.

Seminar 6 Theoretical part

3016 Oxidation of ricinoleic acid (from castor oil) with KMnO 4 to azelaic acid

CCMR Educational Programs

QUESTION 1 Fats and oils vary in their degree of solubility in aqueous solutions. Give a reason for this observation.

ANIMAL OILS AND FATS CHAPTER 10 ÉTHAL 1 1. COMPOSITION 479. BY WEIGHT BY VOLUME 2

Question 2. Choose the correct reaction that happens during hydrogenation of vegetable oil. 1.

Biological Molecules B Lipids, Proteins and Enzymes. Triglycerides. Glycerol

22. The Fischer Esterification

Transcription:

FATS AND SAP: SAPNIFIATIN PURPSE: To synthesize soap from fat and lye. To observe the physical and chemical properties of soap. FATTY AIDS AND FATS: Fats and oils are mixtures of complex esters. Fat esters are made from long chain carboxylic acids (called fatty acids) and an alcohol containing three groups (called glycerol). A common fat is called a triacylglycerol or triglyceride. The hydrocarbon chain of the fatty acids determines the physical and chemical properties of the compound. Triacylglycerols made from long-chain (-16 to -18) saturated fatty acids (like palmitic and stearic acids) are solid or semisolid at room temperature. Solid animal fats contain an abundance of long saturated fatty acids. Triglycerides made from long-chain unsaturated fatty acids (like oleic or linoleic acids) are liquid oils at room temperature. Liquid vegetable oils contain an abundance of long unsaturated fatty acids. A few oils owe their characteristic liquid nature to the presence of shorter chain fatty acids (-6 to -14). oconut oil contains large amounts of lauric (-12) and myristic (-14) acids, as well as smaller amounts of -6, -8, and -10 acids. SAP: ydrolysis of an ester is the reverse of the synthesis of an ester. ydrolysis of a triacylglycerol into glycerol and fatty acids can be catalyzed by either strong acid or strong base. The general process of hydrolyzing esters with caustic alkali s (strong bases such as sodium hydroxide, Na or potassium hydroxides, K) is called saponification. The products of basic hydrolysis of fats or oils are glycerol and the salts of fatty acids called soaps. The term saponification comes from the ancient art of soap-making, performed by heating fats and oils with potash (potassium hydroxide) or lye (sodium hydroxide) solution obtained from leaching wood ashes with slaked lime.

2 Glyceryl Tristearate (A Fat) Na, 2 Glycerol 1,2,3-propantriol + Na Na Na Sodium Stearates (A Soap) Polar hydrophilic end attracts water Nonpolar lipophilic end attracts grease Soap owes its cleaning ability to the formation of micelles which can encapsulate grease or oil and make it water soluble. Micelles are destroyed by hard water ions such as a 2+ and Mg 2+. These ions precipitate the fatty acid anions causing a scum to form. In recent years, synthetic detergents (called syndets ) have been developed which are less affected by hard water ions since the magnesium and calcium salts are quite a bit more soluble. A Micelle Na S A Detergent

3 PREDURES: ATINS: I. SAP: A. Preparation: 1. Into a porcelin evaporating dish pour 2 mls vegetable oil 1 3 mls ethanol 2 20 drops 50% Sodium hydroxide (Na) 3 Stir with a stirring rod to mix well. 2. eat the mixture gently over medium heat on a hot plate or the moderate flame of a laboratory burner. Stir constantly until it becomes a thick paste. 4 3. Allow the dish to cool and record your observations on the report sheet. 4. Place the soap you just prepared into a 150 ml beaker with about 50 mls of deionized water. eat the mixture, with stirring, until all of the solid soap has dissolved in the water. 5 5. Test the p of this soap solution and record the result. 6 Use this soap solution in each of the following procedures. B. Purification: 1. btain two 50 ml beakers. Into beaker #1 pour 10 mls of the soap solution you just made and allow it to cool. 2. Into beaker, #2, pour 10 mls of a detergent solution. 3. To each beaker add solid sodium chloride (Nal) a little at a time with stirring, until no more Nal dissolves and the bottom of the beaker is covered with Nal. Record your observations on the report sheet 7. 4. Remove the mass of pure soap floating on the surface of beaker #1. This could be done by scraping it off the top with a spatula or piece of filter paper. 5. Put a small piece of the purified soap into a test tube and dissolve it in deionized water. Stopper the tube and shake the soap to see if it lathers. 8 6. Test the p of the purified soap solution in the test tube and also test the p of the detergent solution in the second beaker. Record the results. 1 Vegetable oils, or solid animal fat would work as they are all triacylglycerols. 2 Ethanol is a good solvent to dissolve both the nonpolar oil and the polar Na in order to better mix them together. 3 Sodium ydroxide (50% Na) is extremely dangerous. Make certain you are wearing eye protection. Do your best to avoid splashes. If skin contact is made wash immediately with soap and lots of water. 4 Do not overheat and burn your soap. 5 If there are clumps that will not dissolve, scoop them out and discard them. 6 This soap solution contains some leftover sodium hydroxide that didn t react so it will show a very basic p. The crude basic soap is too harsh to use on your skin so it must be purified. 7 Soap can be forced out of solution by dissolving Nal in it. Water can only dissolve a limited amount of stuff and since Nal is more polar than the long hydrocarbon chain of the soap, the water lets go of the soap and dissolves the Nal. The soap that has been let go floats to the surface of the water. The Na leftover from the preparation of soap reaction is very polar like sodium chloride so stays dissolved in the water. Therefore, the soap that comes to the surface of the water is now more pure. 8 You could also test the lathering ability by using the purified soap to wash your hands.

4. Reactivity with ard Water Ions: 1. btain two test tubes. Into test tube #1 pour 5 mls of the unpurified soap solution. Into test tube #2 pour 5 mls of detergent solution. 2. Add up to 10 drops of 1M alcium hloride (al 2 ), one drop at a time, to each tube and observe if a precipitate forms. 3. Record the results. 9 D. Reactivity with Acid: 4. btain two test tubes. Into test tube #1 pour 5 mls of the unpurified soap solution. Into test tube #2 pour 5 mls of detergent solution. 5. Add up to 4 drops of 6M l (hydrochloric acid), one drop at a time to each test tube and observe if a precipitate forms. 9 The sodium salts of fatty acids, soaps, are soluble in water. When other metal ions like calcium, magnesium, or iron, form salts with fatty acids they are not as soluble in water and tend to precipitate out. 10 A soap is a weak base so it reacts with l by taking an + which turns it into a carboxylic acid. The newly made carboxylic acid is a fatty acid with a long hydrocarbon chain and now that it has no charge it is no longer soluble in water. 6. Record the results. 10

5 FATS & SAP REPRT: I. SAP: NAME DATE bservations A. Preparation Appearance of freshly made soap: p of crude soap dissolved in water: B. Purification Results of salting out the soap: Describe the lather after shaking: Results of salting out detergent: p p of purified soap dissolved in water: p of detergent solution:. Reaction with ard Water Ions Results of adding al 2 to soap: Results of adding al 2 to detergent: omplete the reaction: Na 9 Sodium leate 18 + al 2 D. Reaction with Acid Results of adding to l soap: Results of adding l to detergent: omplete the reaction: Na 9 Sodium leate 18 + l

6 FATS & SAP: EXERISES: 1. 2. 3. Salting works to purify soap because. A. Salt kills bacteria that would make soap impure. B. Soap is not as soluble in water as salt is.. Salt (Nal) undergoes a chemical reaction with soap to make a less soluble product that can precipitate. D. More than one of these. What is the advantage of using detergent instead of soap if you have hard water? A. Detergent reacts with hard water ions to form new compounds that are soluble in water. B. Soap reacts with the ions in hard water and forms insoluble soap scum solids.. Detergent is cheaper than soap. D. More than one of these. Soaps and detergents dissolve in both nonpolar oil and in polar water because A. they have a nonpolar ionic end that attracts oil and a polar hydrocarbon end that attracts water. B. they have a nonpolar ionic end that attracts water and a polar hydrocarbon end that attracts oil.. they have a polar ionic end that attracts water and a nonpolar hydrocarbon end that attracts oil. D. Soaps and detergents are neither polar nor nonpolar so the solvent doesn t matter. 4. omplete the following: Na 2 Glyceryl Trioleate