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Page 1: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

1© 2013 Pearson Education, Inc. Chapter 17, Section 1

General, Organic, and Biological Chemistry

Fourth EditionKaren Timberlake

© 2013 Pearson Education, Inc.

17.1Lipids

Chapter 17Lipids

Lectures

Page 2: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

2© 2013 Pearson Education, Inc. Chapter 17, Section 1

Lipids

Lipids are biomolecules that contain fatty acids or a steroid

nucleus. soluble in organic solvents, but not in water. named for the Greek word lipos, which means “fat.” extracted from cells using nonpolar organic solvents. natural components of cell membranes, fat-soluble

vitamins, and steroid hormones.

Page 3: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

3© 2013 Pearson Education, Inc. Chapter 17, Section 1

Lipids

There are 2 types of lipids; those that contain the structural component of a fatty

acid; and

those that contain the structural component of a four member steroid molecule.

Page 4: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

4© 2013 Pearson Education, Inc. Chapter 17, Section 1

Types of Lipids

The lipids that contain fatty acids are waxes, fats and oils (triacylglycerols), glycerophospholipids, and prostaglandins.

The types of lipids that do not contain fatty acid chainsare steroids.

Page 5: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

5© 2013 Pearson Education, Inc. Chapter 17, Section 1

Types of Fatty Acid Lipids

Page 6: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

6© 2013 Pearson Education, Inc. Chapter 17, Section 1

Learning Check

Which lipids contain the alcohol glycerol?

A. steroids and waxes

B. triacylglycerols and glycerophospholipids

C. sphingolipids and glycerophospholipids

D. glycerophospholipids and waxes

Page 7: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

7© 2013 Pearson Education, Inc. Chapter 17, Section 1

Solution

Which lipids contain the alcohol glycerol?

A. steroids and waxes

B. triacylglycerols and glycerophospholipids

C. sphingolipids and glycerophospholipids

D. glycerophospholipids and waxes

Answer is B. Triacylglycerols and glycerophospholipidscontain the alcohol glycerol.

Page 8: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

8© 2013 Pearson Education, Inc. Chapter 17, Section 1

General, Organic, and Biological Chemistry

Fourth EditionKaren Timberlake

© 2013 Pearson Education, Inc.

17.2Fatty Acids

Chapter 17Lipids

Lectures

Page 9: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

9© 2013 Pearson Education, Inc. Chapter 17, Section 1

Fatty Acids

Fatty acids contain long-chain

hydrocarbons with a carboxylic acid.

typically contain 12 to 18 carbon atoms.

are insoluble in water. can be saturated or

unsaturated.

Page 10: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

10© 2013 Pearson Education, Inc. Chapter 17, Section 1

Fatty Acid Formulas

The formulas for fatty acids are written as condensed structural formulas. skeletal formulas.

Insert structures of lauric acid pg 600, both condensed structural formula and skeletal formulas

Page 11: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

11© 2013 Pearson Education, Inc. Chapter 17, Section 1

Saturated fatty acids have only single C—C bonds. molecules that fit closely together

in a regular pattern. have properties similar to alkanes.

Saturated Fatty Acids

Page 12: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

12© 2013 Pearson Education, Inc. Chapter 17, Section 1

Saturated Fatty Acids

Page 13: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

13© 2013 Pearson Education, Inc. Chapter 17, Section 1

Unsaturated Fatty Acids

Unsaturated fatty acids have one or more double bond. that are naturally occurring have one or more cis

double bond

insert picture of cis and trans fatty acid from top of pg 602

Page 14: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

14© 2013 Pearson Education, Inc. Chapter 17, Section 1

Monounsaturated Fatty Acids

Unsaturated fatty acids with one double bond are called monounsaturated fatty acids.

Insert table 17.1 monounsaturated fatty acids.

Page 15: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

15© 2013 Pearson Education, Inc. Chapter 17, Section 1

Polyunsaturated Fatty Acids

Unsaturated fatty acids with more than one double bond are called polyunsaturated fatty acids.

Insert table 17.1 polyunsaturated fatty acids.

Page 16: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

16© 2013 Pearson Education, Inc. Chapter 17, Section 1

Properties of Saturated Fatty AcidsSaturated fatty acids fit closely together in a

regular pattern. have significant

dispersion forces between chains.

have higher melting points.

are solids at room temperature.

Page 17: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

17© 2013 Pearson Education, Inc. Chapter 17, Section 1

Properties of Unsaturated Fatty AcidsUnsaturated fatty acids have “kinks” in the fatty

acid chains. do not pack closely. have fewer attractions

between chains. have lower melting points. are liquids at room

temperature.

“kinks” in chain

Page 18: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

18© 2013 Pearson Education, Inc. Chapter 17, Section 1

Learning Check

Assign the melting point (mp) of −17°C, 13°C, or 69°C to each one of the following 18-carbon fatty acids, and list the fatty acids in order from highest to lowest melting point. Explain.

A. oleic acid

B. stearic acid

C. linoleic acid

Page 19: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

19© 2013 Pearson Education, Inc. Chapter 17, Section 1

Solution

Stearic acid is saturated and would have a higher melting point than the unsaturated fatty acids. Oleic acid, which has one double bond, has a higher mp than linoleic acid, which has two double bonds.

B. stearic acid mp 69°C saturatedA. oleic acid mp 13°C unsaturated with one

double bond C. linoleic acid mp −17°C unsaturated with two

double bonds

Page 20: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

20© 2013 Pearson Education, Inc. Chapter 17, Section 1

Prostaglandins

Prostaglandins have 20 carbon atoms in their fatty acid chains. differ by the substituents attached to the 5-carbon

ring.

Page 21: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

21© 2013 Pearson Education, Inc. Chapter 17, Section 1

Prostaglandins and Physiological Effects

Prostaglandins have potent physiological effects. Some increase blood pressure. Some lower blood pressure. Some stimulate contractions and relaxation of smooth

muscle in the uterus during the birth process and menstrual cycle.

When tissues are injured, arachidonic acid in the bloodis converted to PGE1 and PGF2 that produceinflammation and pain in the area.

Page 22: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

22© 2013 Pearson Education, Inc. Chapter 17, Section 1

NSAIDs and Prostaglandins

Several nonsteroidal anti-inflammatory drugs (NSAIDs), such as aspirin, block production of prostaglandins decreasing pain, inflammation, and fever.

Insert Picture of arachidonic acid conversion, top page 605.

Page 23: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

23© 2013 Pearson Education, Inc. Chapter 17, Section 1

NSAIDs and Prostaglandins

Other NSAIDs include naproxen (Aleve and Naprosyn), ketoprofen (Actron), and nabumetone (Relafen).

Long-term use of such products can result in liver, kidney, and gastrointestinal damage.

Page 24: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

24© 2013 Pearson Education, Inc. Chapter 17, Section 1

Omega-3 and Omega-6 Fatty Acids

Fish and vegetable oils have high levels of unsaturated fats. In vegetable oils, they are mostly omega-6 with

the first at C6.

Linoleic acid

In fish oils, they are mostly omega-3 with the first at C3. CH3─CH2─(CH═CH─CH2)3─(CH2)6─COOH 1 3

Linolenic acid

Page 25: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

25© 2013 Pearson Education, Inc. Chapter 17, Section 1

Omega-6 and Omega-3 Fatty Acids

Page 26: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

26© 2013 Pearson Education, Inc. Chapter 17, Section 1

Omega-3 Fatty Acids

Omega-3 fatty acids lower the tendency of blood platelets to stick

together, thereby reducing the possibility of blood clots.

can help reduce risk of heart disease. are found in salmon, tuna, and herring.

Page 27: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

27© 2013 Pearson Education, Inc. Chapter 17, Section 1

Learning Check

Draw the condensed structural formulas for each of the fatty acids with 10 carbon atoms that follow.

A. saturated

B. monounsaturated omega-3

C. monounsaturated omega-6

Page 28: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

28© 2013 Pearson Education, Inc. Chapter 17, Section 1

Solution

Draw the condensed structural formulas for each of the fatty acids with 10 carbon atoms that follow.

A. saturated

CH3—CH2—CH2—CH2—CH2—CH2—CH2—CH2—CH2—COOH

B. monounsaturated omega-3

C. monounsaturated omega-6

Page 29: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

29© 2013 Pearson Education, Inc. Chapter 17, Section 1

General, Organic, and Biological Chemistry

Fourth EditionKaren Timberlake

© 2013 Pearson Education, Inc.

17.3Waxes and

Triacylglycerols

Chapter 17Lipids

Lectures

Page 30: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

30© 2013 Pearson Education, Inc. Chapter 17, Section 1

Waxes

Waxes are esters of saturated fatty acids and long-chain alcohols

each containing 14 to 30 carbon atoms. coatings that prevent loss of water from leaves of plants.

Page 31: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

31© 2013 Pearson Education, Inc. Chapter 17, Section 1

Typical Waxes

Page 32: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

32© 2013 Pearson Education, Inc. Chapter 17, Section 1

Fats and Oils: Triacylglycerols

Fats and oils are also called triacylglycerols. triesters of glycerol. produced by esterification. formed when the hydroxyl

groups of glycerol react with the carboxyl groups of fatty acids.

a major form of energy storage for animals.

Insert picture of polar bear pg 608

Page 33: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

33© 2013 Pearson Education, Inc. Chapter 17, Section 1

In a triacylglycerol, glycerol forms ester bonds with three fatty acids.

Triacylglycerols

Insert structure top pg 608 as shown:

Page 34: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

34© 2013 Pearson Education, Inc. Chapter 17, Section 1

Formation of a Triacylglycerol

Most naturally occurring fats and oils are mixed triacylglycerols that contain glycerol bonded by ester bonds to two or three different fatty acids, typically palmitic acid, linoleic acid, and stearic acid.

One possible structure follows.

Page 35: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

35© 2013 Pearson Education, Inc. Chapter 17, Section 1

Learning Check

What are the fatty acids in the following triacylglycerol?

CH2 (CH2)12 CH3

CH2

CH CH CH (CH2)7 CH3O (CH2)7C

O

O (CH2)16 CH3C

O

O

O

C

Page 36: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

36© 2013 Pearson Education, Inc. Chapter 17, Section 1

Solution

Stearic acid

Oleic acid

Myristic acidCH2 (CH2)12 CH3

CH2

CH CH CH (CH2)7 CH3O (CH2)7C

O

O (CH2)16 CH3C

O

O

O

C

Page 37: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

37© 2013 Pearson Education, Inc. Chapter 17, Section 1

Learning Check

Draw the condensed structural formula for glyceryl tripalmitoleate (tripalmitolein).

Page 38: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

38© 2013 Pearson Education, Inc. Chapter 17, Section 1

Solution

Draw the condensed structural formula for glyceryl tripalmitoleate (tripalmitolein).

Page 39: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

39© 2013 Pearson Education, Inc. Chapter 17, Section 1

Melting Points of Fats and Oils

A triacylglycerol that is usually called a fat is solid at room temperature. is prevalent in meats, whole milk, butter, and cheese.

A triacylglycerol that is usually called an oil is liquid at room temperature. is prevalent in plants, such as olive and safflower.

Page 40: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

40© 2013 Pearson Education, Inc. Chapter 17, Section 1

Oils with Unsaturated Fatty Acids

Oils have more unsaturated fats. have cis double bonds that cause “kinks” in the fatty

acid chains. cannot pack triacylglycerol molecules as closely

together as in fats. have lower melting points than do saturated fats. are liquids at room temperature.

Page 41: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

41© 2013 Pearson Education, Inc. Chapter 17, Section 1

Triacylglycerol with Unsaturated Fatty AcidsUnsaturated fatty acid chains have kinks that do not allow close packing, such as those in olive oil.

Page 42: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

42© 2013 Pearson Education, Inc. Chapter 17, Section 1

Saturated and Unsaturated Fatty Acids In Fats and Oils

Vegetable oils are liquids at room temperature because they have a higher percentage of unsaturated fatty acids than do animal fats.

Page 43: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

43© 2013 Pearson Education, Inc. Chapter 17, Section 1

General, Organic, and Biological Chemistry

Fourth EditionKaren Timberlake

© 2013 Pearson Education, Inc.

17.4Chemical Properties of

Triacylglycerols

Chapter 17Lipids

Lectures

Page 44: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

44© 2013 Pearson Education, Inc. Chapter 17, Section 1

The chemical reactions of triacylglycerols are similarto those of alkenes and esters. In hydrogenation, double bonds in unsaturated

fatty acids react with H2 in the presence of a Ni or Pt catalyst.

In hydrolysis, ester bonds are split by water in the presence of an acid, a base, or an enzyme.

Chemical Properties of Triacylglycerols

Page 45: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

45© 2013 Pearson Education, Inc. Chapter 17, Section 1

Hydrogenation of Glyceryl Trioleate

In a hydrogenation reaction, H2 adds across the double bond to form a carbon–carbon single bond.

Page 46: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

46© 2013 Pearson Education, Inc. Chapter 17, Section 1

Hydrogenation of Oils

The hydrogenation of oils converts double bonds to single bonds, adds hydrogen (H2) to the carbon atoms of double

bonds, increases the melting point, and produces solids, such as margarine and shortening

Page 47: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

47© 2013 Pearson Education, Inc. Chapter 17, Section 1

Learning Check

Which of the following products is obtained from the complete hydrogenation of glyceryl trioleate?

A. glycerol and 3 oleic acids

B. glyceryltristearate

C. glycerol and 3 stearic acids

Page 48: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

48© 2013 Pearson Education, Inc. Chapter 17, Section 1

Which of the following products is obtained from the complete hydrogenation of glyceryl trioleate?

B. glyceryltristearate

Solution

Page 49: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

49© 2013 Pearson Education, Inc. Chapter 17, Section 1

Olestra, a Fat Substitute

Olestra is used in foods as an artificial fat. composed of 6–8 long-chain fatty acids attached by

ester links to a sucrose (not glycerol) molecule. not broken down in the intestinal tract.

Page 50: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

50© 2013 Pearson Education, Inc. Chapter 17, Section 1

Unsaturated fatty acids can be cis with bulky groups on the same side of , or

trans with bulky groups on opposite sides of .

Cis and Trans Fatty Acids

Page 51: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

51© 2013 Pearson Education, Inc. Chapter 17, Section 1

Trans Fatty Acids and Hydrogenation Trans fatty acids are formed during hydrogenation when cis double

bonds are converted to an undesirable side product with a trans double bond.

in the body behave like saturated fatty acids. are estimated to make up 2–4% of our total

calories.

The American Heart Association recommends the use of soft margarine, which is only slightly hydrogenated and therefore has fewer trans fatty acids.

Page 52: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

52© 2013 Pearson Education, Inc. Chapter 17, Section 1

Trans Fats

In vegetable oils, the unsaturated fats usually contain cis double

bonds. during hydrogenation, some cis double bonds are

converted to trans double bonds (more stable), causing a change in the fatty acid structure.

Page 53: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

53© 2013 Pearson Education, Inc. Chapter 17, Section 1

Formation of Trans Fats

Page 54: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

54© 2013 Pearson Education, Inc. Chapter 17, Section 1

Learning Check

Identify each statement as true (T) or false (F).

A. There are more unsaturated fats in vegetable oils.

B. Vegetable oils have higher melting points than fats.

C. Hydrogenation of oils converts some cis-double bonds to trans-double bonds.

D. Animal fats have more saturated fats.

Page 55: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

55© 2013 Pearson Education, Inc. Chapter 17, Section 1

Solution

Identify each statement as true (T) or false (F).

T A. There are more unsaturated fats in vegetable oils.

F B. Vegetable oils have higher melting points than fats.

T C. Hydrogenation of oils converts some cis-double bonds to trans-double bonds.

T D. Animal fats have more saturated fats.

Page 56: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

56© 2013 Pearson Education, Inc. Chapter 17, Section 1

Hydrolysis

In acid or enzyme hydrolysis, water adds to the ester bonds. triacylglycerols hydrolyze forming glycerol and three

fatty acids. a strong acid, such as HCl or H2SO4, or an enzyme

catalyst is required.

Page 57: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

57© 2013 Pearson Education, Inc. Chapter 17, Section 1

Base Hydrolysis (Saponification )

In base hydrolysis (saponification), a triacylglycerol reacts with heat and a strong base. a triacylglycerol splits into glycerol and the salts of

fatty acids (soap). a solid soap that can be molded into a desired shape

is produced when NaOH is used. a softer, liquid soap is produced when KOH is used. polyunsaturated oils produce softer soaps.

Page 58: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

58© 2013 Pearson Education, Inc. Chapter 17, Section 1

Saponification

glycerol + salts of fatty acids (soap)Fat or oil + strong base

Page 59: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

59© 2013 Pearson Education, Inc. Chapter 17, Section 1

Summary of Organic and Lipid Reactions

Page 60: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

60© 2013 Pearson Education, Inc. Chapter 17, Section 1

What products are obtained from the complete hydrolysis of glyceryl trioleate?

A. glycerol and 3 oleic acids

B. glyceryl tristearate

C. glycerol and 3 stearic acids

Learning Check

Page 61: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

61© 2013 Pearson Education, Inc. Chapter 17, Section 1

What products are obtained from the complete hydrolysis of glyceryl trioleate?

A. glycerol and 3 oleic acids

Solution

Page 62: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

62© 2013 Pearson Education, Inc. Chapter 17, Section 1

Learning Check

Draw the condensed structural formula of theproduct of the following reaction.

O

O

CH2

O

O

CH

CH2 O

O

C

C

C

(CH2)7 CH CH

CHCH(CH2)7

CHCH(CH2)7

(CH2)5 CH3

(CH2)5 CH3

(CH2)5 CH3

+ 3H2

Ni

Page 63: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

63© 2013 Pearson Education, Inc. Chapter 17, Section 1

Solution

CH2 (CH2)14

CH2

CH O C

O

O C

O

O

O

C

(CH2)14 CH3

(CH2)14 CH3

CH3

Page 64: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

64© 2013 Pearson Education, Inc. Chapter 17, Section 1

General, Organic, and Biological Chemistry

Fourth EditionKaren Timberlake

© 2013 Pearson Education, Inc.

17.5Phospholipids

Chapter 17Lipids

Lectures

Page 65: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

65© 2013 Pearson Education, Inc. Chapter 17, Section 1

Glycerophospholipids, themost abundant lipids in cellmembranes, contain two fatty acids, which form ester

bonds with the first and second hydroxyl group of glycerol.

a third hydroxyl group, which forms an ester with phosphoric acid, which then forms another phosphoester bond with an amino alcohol.

Glycerophospholipids

Insert pictureof glycerophospholipidpg 618

Page 66: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

66© 2013 Pearson Education, Inc. Chapter 17, Section 1

Lecithin and cephalin are glycerophospholipids that are abundant in brain and nerve tissues. are found in egg yolk, wheat germ, and yeast. contain choline (in lecithins) or either ethanolamine or

serine (in cephalins).

Lecithin and Cephalin

Page 67: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

67© 2013 Pearson Education, Inc. Chapter 17, Section 1

Glycerophospholipids Contain Amino Alcohols. Three amino alcohols found in glycerophospholipids

are choline, serine, and ethanolamine. In the body, at a physiological pH of 7.4, these amino

alcohols are ionized.

Insert structures of amino alcohols pg 618 bottom

Page 68: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

68© 2013 Pearson Education, Inc. Chapter 17, Section 1

Glycerophospholipids are Polar and Nonpolar. Glycerophospholipids have both polar and nonpolar regions that allow them to

interact with polar and nonpolar substances. an ionized amino alcohol and phosphate portion,

called “the head,” which is polar and strongly attracted to water.

a hydrocarbon chain known as “the tail,” which is soluble in nonpolar substances.

Page 69: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

69© 2013 Pearson Education, Inc. Chapter 17, Section 1

Formation of GlycerophospholipidsThe formation of a glycerophospholipid occurs when ester bonds form between glycerol and two fatty acids, and two phosphoester bonds form between phosphoric acid and an ionized amino alcohol and glycerol, such as palmitic acid.

Page 70: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

70© 2013 Pearson Education, Inc. Chapter 17, Section 1

Components of GlycerophospholipidsThe components of a glycerophospholipid are choline, phosphoric acid, glycerol, and two fatty acids.

Insert structure from figure 17.6a

Page 71: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

71© 2013 Pearson Education, Inc. Chapter 17, Section 1

Components of GlycerophospholipidsIn a glycerophospholipid, a polar “head” contains the ionized amino alcohol and phosphate, while the hydrocarbon chains of two fatty acids make up the nonpolar “tails.”

Insert structure from figure 17.6b

Page 72: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

72© 2013 Pearson Education, Inc. Chapter 17, Section 1

Learning Check

Identify each as a fatty acid, triacylglycerol, amino alcohol or glycerophospholipid.

A. glyceryl trioleate

B. cephalin

C. choline

D. palmitic acid

Page 73: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

73© 2013 Pearson Education, Inc. Chapter 17, Section 1

Solution

Identify each as a fatty acid, triacylglycerol, amino alcohol or glycerophospholipid.

A. glyceryl trioleate triacylglycerol

B. cephalin glycerophospholipid

C. choline amino alcohol

D. palmitic acid fatty acid

Page 74: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

74© 2013 Pearson Education, Inc. Chapter 17, Section 1

Learning Check

Identify the components and type of glycerophospholipid. O ║CH2—O—C— (CH2)16—CH3

O ║CH2—O—C— (CH2)16—CH3

+

O NH3

║ │CH2—O—P—O—CH2—CH−COO –

│ O–

Page 75: 1 © 2013 Pearson Education, Inc. Chapter 17, Section 1 General, Organic, and Biological Chemistry Fourth Edition Karen Timberlake © 2013 Pearson Education,

75© 2013 Pearson Education, Inc. Chapter 17, Section 1

Solution

Identify the components and type of glycerophospholipid. O ║CH2—O—C— (CH2)16—CH3

O 2 Stearic acids

║CH2—O—C— (CH2)16—CH3

+

O NH3

║ │ Type = cephalinCH2—O—P—O—CH2—CH−COO –

│ Serine O– Phosphate Amino alcohol

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Sphingosine

Sphingosine is an 18-carbon unsaturated amino alcohol.

Insert structure top pg 621

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Sphingolipids

Sphingolipids are phospholipids that contain a long-chain amino alcohol called sphingosine, rather than glycerol.

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Sphingomyelins

Sphingomyelins, are a group of sphingolipids in which the amine group forms an amide bond to a fatty acid,

and the hydroxyl group of sphingosine forms an ester

bond with phosphate forming another phosphoester bond to an amino alcohol, such as choline.

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79© 2013 Pearson Education, Inc. Chapter 17, Section 1

Sphingomyelins

Sphingomyelins, are abundant in the white matter of the myelin sheath, a coating

surrounding the nerve. cells that increase the speed of nerve impulses and

insulate and protect the nerve cells.

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Multiple Sclerosis

In multiple sclerosis, sphingomyelin is lost from the myelin sheath, which

protects the neurons in the brain and spinal cord. scars form on the neurons and impair the

transmission of nerve signals.

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81© 2013 Pearson Education, Inc. Chapter 17, Section 1

General, Organic, and Biological Chemistry

Fourth EditionKaren Timberlake

© 2013 Pearson Education, Inc.

17.6Steroids

Chapter 17Lipids

Lectures

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82© 2013 Pearson Education, Inc. Chapter 17, Section 1

Steroid Nucleus

Steroid molecules contain a steroid nucleus with3 cyclohexane rings, 1 cyclopentane ring,no fatty acids, anda total of four rings A, B, C, D.

The steroid nucleus is numbered from the carbon atoms in ring A to two methyl groups at 18 and 19.

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83© 2013 Pearson Education, Inc. Chapter 17, Section 1

Cholesterol

Cholesterol is the most important and abundant steroid in

the body. is a sterol because it contains an oxygen atom

as a hydroxyl group, –OH on carbon 3. has a double bond between carbon 5 and

carbon 6. has methyl –CH3 groups, at carbon 10 and 13.

has a carbon chain at carbon 17.

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84© 2013 Pearson Education, Inc. Chapter 17, Section 1

Cholesterol

Cholesterol is a component of cellular membranes, myelin sheaths, and brain and nerve tissues.

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85© 2013 Pearson Education, Inc. Chapter 17, Section 1

Cholesterol in the Body

Cholesterol in the body

is obtained from meats, milk, and eggs and synthesized in the liver.

clogs arteries when high levels form plaque.

A normal, open artery.

An artery clogged by cholesterol plaque

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86© 2013 Pearson Education, Inc. Chapter 17, Section 1

Cholesterol in Foods

A typical American diet includes 400–500 mg of cholesterol per day.

The American Heart Association has recommended no more than 300 mg of cholesterol per day.

Saturated fats in the diet may stimulate the production of cholesterol by the liver.

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87© 2013 Pearson Education, Inc. Chapter 17, Section 1

Learning Check

Match the components of the cholesterol molecule witheach of the following:

alkyl chain hydroxyl group

steroid nucleus methyl group

CH3

CH3CH3

CH3

HO

CH3

AC

B

D

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88© 2013 Pearson Education, Inc. Chapter 17, Section 1

Solution

Match the components of the cholesterol molecule witheach of the following:

alkyl chain hydroxyl group

steroid nucleus methyl group

CH3

CH3CH3

CH3

HO

CH3

AC

B

D

D A

C B

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89© 2013 Pearson Education, Inc. Chapter 17, Section 1

Bile Salts

Bile salts are synthesized from cholesterol in the liver. are stored in the gallbladder and secreted into the

small intestine. have a polar and a nonpolar region. help in the absorption of cholesterol into the intestinal

mucosa.

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Sodium Glycocholate, a Bile Salt

Nonpolar region

Polar region

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91© 2013 Pearson Education, Inc. Chapter 17, Section 1

Gallstones

Gallstones are formed when large amounts of cholesterol

accumulate in the gallbladder. composed of almost 100% cholesterol, with some

calcium salts, fatty acids, and glycerophospholipids.

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92© 2013 Pearson Education, Inc. Chapter 17, Section 1

Lipoproteins

Lipoproteins are spherical particles with an outer surface of polar

proteins and glycerophospholipids that surround hundreds of nonpolar molecules of triacylglycerols and cholesteryl esters.

combine lipids with proteins and phospholipids. are soluble in water because the surface consists of

polar lipids.

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Lipoproteins

A spherical lipoprotein particle surrounds nonpolar lipids with polar lipids and protein for transport to body cells.

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94© 2013 Pearson Education, Inc. Chapter 17, Section 1

Types of Lipoproteins

Lipoproteins differ in density, composition, and function

and include chylomicrons, very low-density lipoprotein (VLDLs); low-density lipoproteins (LDLs), which carry

cholesterol to the tissues; and high-density lipoproteins (HDLs) that pick up

cholesterol from the tissues and carry it to the liver.

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95© 2013 Pearson Education, Inc. Chapter 17, Section 1

LDLs

LDLs transport cholesterol to tissues where it can be used

for synthesis of cell membranes and steroid hormones.

deposit cholesterol in the arteries in the form of plaque when cholesterol levels exceed levels needed by tissues.

called “bad” cholesterol for their contribution to heart disease.

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HDLs

HDLs are more dense than LDLs due to the increased

amount of protein present. pick up cholesterol from the tissues and carry it to the

liver, where it can be converted to bile salts, which are eliminated from the body,

are called “good” cholesterol.

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VLDLs

VLDLs carry the triacylglycerols synthesized in the liver to the adipose tissues for storage.

Insert fig 17.10 pg 626

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Lipid Panel

A lipid panel is a blood test that measures serum lipidlevels including cholesterol triglycerides high-density lipoprotein (HDL) low-density lipoprotein (LDL)

The results of a lipid panel are used to evaluate apatient’s risk of heart disease.

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Lipid Panel

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Steroid Hormones

Steroid hormones are chemical messengers in cells. are produced from cholesterol. include sex hormones, such as androgens

(testosterone) in males and estrogens (estradiol) in females.

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Steroid Hormones

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102© 2013 Pearson Education, Inc. Chapter 17, Section 1

Adrenal Corticosteroids

Adrenal corticosteroids are steroid hormonesproduced by the adrenal glands located on the topof each kidney and include aldosterone, which regulates electrolytes and

water balance by the kidneys; cortisol, released under stress to increase blood

sugar and regulate carbohydrate, fat, and protein metabolism; and

prednisone, a synthetic corticosteroid, derived from cortisone, used for reducing inflammation, treating asthma and rheumatoid arthritis.

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Adrenal Corticosteroids

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104© 2013 Pearson Education, Inc. Chapter 17, Section 1

Learning Check

Identify each of the following as a steroid, triacylglycerol, phospholipid, or sphingolipid.

A. cholesterol

B. glycerol, 2 fatty acids, phosphate, and choline

C. glyceryl tristearate

D. sphingosine, fatty acid, phosphate, and choline

E. estradiol

F. bile salts

G. lipids in plasma membranes

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105© 2013 Pearson Education, Inc. Chapter 17, Section 1

Solution

A. cholesterol steroid

B. glycerol, 2 fatty acids, phospholipid

phosphate, and choline

C. glyceryl tristearate triacylglycerol

D. sphingosine, fatty acid, sphingolipid

phosphate, and choline

E. estradiol steroid

F. bile salts steroid

G. lipids in plasma phospholipid

membranes sphingolipid

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106© 2013 Pearson Education, Inc. Chapter 17, Section 1

General, Organic, and Biological Chemistry

Fourth EditionKaren Timberlake

© 2013 Pearson Education, Inc.

17.7Cell Membranes

Chapter 17Lipids

Lectures

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107© 2013 Pearson Education, Inc. Chapter 17, Section 1

Cell Membranes

Cell membranes have a lipid bilayer that separates cellular contents from the external

environment. contains two layers of glycerophospholipids arranged

with their hydrophilic heads at the outer and inner membrane surfaces and their hydrophobic tails in the center.

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108© 2013 Pearson Education, Inc. Chapter 17, Section 1

Fluid Mosaic Model of Cell MembranesThe lipid bilayer contains proteins, carbohydrates, and cholesterol. has unsaturated fatty acids that make cell

membranes fluid-like rather than rigid. has proteins and carbohydrates on the surface that

communicate with hormones and neurotransmitters.

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109© 2013 Pearson Education, Inc. Chapter 17, Section 1

Fluid Mosaic Model

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110© 2013 Pearson Education, Inc. Chapter 17, Section 1

Transport Pathways Through Cell MembranesThe transport of substances through cell membranesinvolves diffusion (passive transport), which moves

particles from a higher to a lower concentration; facilitated transport, which uses protein channels

to increase the rate of diffusion; and active transport, which moves ions against a

concentration gradient.

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Transport Pathways Through Cell Membranes

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112© 2013 Pearson Education, Inc. Chapter 17, Section 1

Learning Check

What is the transport of particles across a cell membranefrom high concentration to low concentration called?

A. facilitated transport

B. diffusion (passive transport)

C. active transport

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113© 2013 Pearson Education, Inc. Chapter 17, Section 1

Solution

What is the transport of particles across a cell membranefrom high concentration to low concentration called?

A. facilitated transport

B. diffusion (passive transport)

C. active transport