Concept explainers
(a)
Interpretation:
A steroid is to be classified as saponifiable or nonsaponifiable lipid.
Concept introduction:
Lipids are one of those macromolecular substances that are present in the living cell. The cell membrane of the living cell is made up of lipids. The lipids have a greasy, waxy and oily texture. The lipids are insoluble in water. They include natural oils, waxes, and steroids.
Answer to Problem 18.4E
A steroid is a nonsaponifiable lipid.
Explanation of Solution
A hydrolysis reaction carried out in a basic solution is known as saponification reaction. The term saponifiable lipids indicate the lipids that can undergo saponification reaction. The lipids that have ester group are saponifiable lipids. The basic structure of steroid is composed of three six-member ring and one five-member ring. The steroid ring system is shown below.
Figure 1
The basic structure of steroid does not have any ester group. Therefore, a steroid is a nonsaponifiable lipid.
A steroid is a nonsaponifiable lipid.
(b)
Interpretation:
Wax is to be classified as saponifiable or nonsaponifiable lipid.
Concept introduction:
Lipids are one of those macromolecular substances that are present in the living cell. The cell membrane of the living cell is made up of lipids. The lipids have a greasy, waxy and oily texture. The lipids are insoluble in water. They include natural oils, waxes, and steroids.
Answer to Problem 18.4E
Wax is a saponifiable lipid.
Explanation of Solution
A hydrolysis reaction carried out in a basic solution is known as saponification reaction. The term saponifiable lipids indicate the lipids that can undergo saponification reaction. The lipids that have ester group are saponifiable lipids. The wax is an ester of long-chain alcohol and a fatty acid. The structure of a simple wax that is beeswax is shown below.
Figure 2
The basic structure of wax has an ester group. Therefore, wax is a saponifiable lipid.
Wax is a saponifiable lipid.
(c)
Interpretation:
A triglyceride is to be classified as saponifiable or nonsaponifiable lipid.
Concept introduction:
Lipids are one of those macromolecular substances that are present in the living cell. The cell membrane of the living cell is made up of lipids. The lipids have a greasy, waxy and oily texture. The lipids are insoluble in water. They include natural oils, waxes, and steroids.
Answer to Problem 18.4E
A triglyceride is a saponifiable lipid.
Explanation of Solution
A hydrolysis reaction carried out in a basic solution is known as saponification reaction. The term saponifiable lipids indicate the lipids that can undergo saponification reaction. The lipids that have ester group are saponifiable lipids. The triglyceride is formed from glycerol and three fatty acids with ester bonds. The general structure of triglyceride is shown below.
Figure 3
The basic structure of triglyceride has ester groups. Therefore, a triglyceride is a saponifiable lipid.
A triglyceride is a saponifiable lipid.
(d)
Interpretation:
A phosphoglyceride is to be classified as saponifiable or nonsaponifiable lipids.
Concept introduction:
Lipids are one of those macromolecular substances that are present in the living cell. The cell membrane of the living cell is made up of lipids. The lipids have a greasy, waxy and oily texture. The lipids are insoluble in water. They include natural oils, waxes, and steroids.
Answer to Problem 18.4E
A phosphoglyceride is a saponifiable lipid.
Explanation of Solution
A hydrolysis reaction carried out in a basic solution is known as saponification reaction. The term saponifiable lipids indicate the lipids that can undergo saponification reaction. The lipids that have ester group are saponifiable lipids. The structure of phosphoglyceride is similar to that of a triglyceride. The only difference between triglyceride and phosphoglyceride is that on the third carbon of glycerol, a phosphate group is attached in the phosphoglyceride. The general structure of phosphoglyceride is shown below.
Figure 4
The basic structure of phosphoglyceride has ester groups. Therefore, a phosphoglyceride is a saponifiable lipid.
A phosphoglyceride is a nonsaponifiable lipid.
(e)
Interpretation:
A glycolipid is to be classified as saponifiable or nonsaponifiable lipid.
Concept introduction:
Lipids are one of those macromolecular substances that are present in the living cell. The cell membrane of the living cell is made up of lipids. The lipids have a greasy, waxy and oily texture. The lipids are insoluble in water. They include natural oils, waxes, and steroids.
Answer to Problem 18.4E
A glycolipid is a saponifiable lipid.
Explanation of Solution
A hydrolysis reaction carried out in a basic solution is known as saponification reaction. The term saponifiable lipids indicate the lipids that can undergo saponification reaction. The lipids that have ester group are saponifiable lipids. The glycolipid contains carbohydrate in it. The glycolipids are also termed as cerebroside as they are present in the brain. The typical structure of glycolipid (cerebroside) is shown below.
Figure 5
The basic structure of glycolipid does not have an ester group but they have an amide group that can undergo saponification. Therefore, a glycolipid is a saponifiable lipid.
A glycolipid is a saponifiable lipid.
(f)
Interpretation:
A prostaglandin is to be classified as saponifiable or nonsaponifiable lipid.
Concept introduction:
Lipids are one of those macromolecular substances that are present in the living cell. The cell membrane of the living cell is made up of lipids. The lipids have a greasy, waxy and oily texture. The lipids are insoluble in water. They include natural oils, waxes, and steroids.
Answer to Problem 18.4E
Prostaglandin is a nonsaponifiable lipid.
Explanation of Solution
A hydrolysis reaction carried out in a basic solution is known as saponification reaction. The term saponifiable lipids indicate the lipids that can undergo saponification reaction. The lipids that have ester group are saponifiable lipids. The basic structure prostaglandin is composed of a five-member ring with two substituted carbon chain. The structure of prostaglandin
Figure 6
The basic structure of prostaglandin does not have an ester group. Therefore, a prostaglandin is a nonsaponifiable lipid.
Prostaglandin is a nonsaponifiable lipid.
Want to see more full solutions like this?
Chapter 18 Solutions
Bundle: Chemistry for Today: General, Organic, and Biochemistry, Loose-Leaf Version, 9th + LMS Integrated OWLv2, 4 terms (24 months) Printed Access Card
- Which of the following attributes is a key advantage of the chiral auxiliary approach over the chiral pool approach in asymmetric synthesis? Question 10Select one: A. Chiral auxiliaries are cheaper than chiral pool substrates B. Chiral auxiliary can be recovered and recycled unlike chiral pool substrates. C. The use of chiral auxiliaries provide enantiopure products, while chiral pool reactions are only enantioselective D. The chiral auxiliaries are naturally occurring and do not require synthesisarrow_forwardIn the following molecule, indicate the hybridization and shape of the indicated atoms. CH3 CH3 H3C HO: CI:arrow_forwardWhich of the following are TRUE about linear syntheses? Question 7Select one: A. They are easier to execute B. They are the most efficient strategy for all syntheses C. They are generally shorter than convergent syntheses D. They are less versatile compared to convergent synthesesarrow_forward
- Which of the following characteristics is common among chiral pool substrates? Question 4Select one: A. They have good leaving groups B. They are all achiral C. All have a multiplicity of chiral centres D. They have poor leaving groupsarrow_forwardDetermine whether the following reaction is an example of a nucleophilic substitution reaction: H NO2 H+ NO 2 + Molecule A Molecule B Is this a nucleophilic substitution reaction? If this is a nucleophilic substitution reaction, answer the remaining questions in this table. What word or two-word phrase is used to describe the role Molecule A plays in this reaction? What word or two-word phrase is used to describe the role Molecule B plays in this reaction? Use a 6 + symbol to label the electrophilic carbon that is attacked during the substitution. Highlight the leaving group on the appropriate reactant. O Yes ○ No ☐ 0 dx 000 HE ?arrow_forwardDraw the major organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. :0: NaOH Harrow_forward
- 5. Calculate the total amount of heat transferred as 50 g of wat Specific heat H₂O (g) 2.00 J/g°C -10 °C. Specific heat H₂O (1) Specific heat H₂O (s) 4.18 J/g°C 2.11 J/g°C Heat of vaporization 2260 J/g Heat of fusion 334 J/g Melting point 0°C 6. Calculate the total amount of heat transferred as 25 g of water is heated from 50 °C to 100 °C as a gas. Boiling point 100 °Carrow_forwardCalculate the total amount of heat transferred as 50 g of Water -10°C. Calculate the total amount of heat transferred as 25 g of water is heated from 50°C to 100°C as a gas. \table[[Specific heat H₂O(g), 2.00°C Η 2 g 5. Calculate the total amount of heat transferred as 50 g of wat Specific heat H₂O (g) 2.00 J/g°C -10 °C. 4.18 J/g°C 2.11 J/g°C 2260 J/g 334 J/g Specific heat H₂O (1) Specific heat H₂O (s) Heat of vaporization Heat of fusion Melting point 6. Calculate the total amount of heat transferred as 25 g of water is heated from 50 °C to 100 °C as a gas. Boiling point 100 °C 0°Carrow_forwardWrite formulas for ionic compounds composed of the following ions. Use units as a guide to your solutions. 24. sodium and nitrate 25. calcium and chlorate 26. aluminum and carbonate 27. CHALLENGE Write the formula for an ionic compound formed by ions from a group 2 element and polyatomic ions composed of only carbon and oxygen.show work step by steparrow_forward
- ADDITIONAL PRACTICE PRACTICE Problems Write formulas for ionic compounds composed of the following ions. Use units as a guide to your solutions. 24. sodium and nitrate 25. calcium and chlorate 26. aluminum and carbonate 27. CHALLENGE Write the formula for an ionic compound formed by ions from a group 2 element and polyatomic ions composed of only carbon and oxygen. ounds 1998arrow_forward7:35 < Dji Question 19 of 22 5G 50% Submit What is the pH of a buffer made from 0.350 mol of HBrO (Ka = 2.5 × 10-9) and 0.120 mol of KBRO in 2.0 L of solution? | 1 2 3 ☑ 4 5 6 C 7 8 ☐ 9 +/- Tap here for additional resources ||| 0 ×10 Гarrow_forwardaw the major substitution products you would expect for the reaction shown below. If substitution would not occur at a significant rate under these conditions, check the box underneath the drawing area instead. Be sure you use wedge and dash bonds where necessary, for example to distinguish between major products. Note for advanced students: you can assume that the reaction mixture is heated mildly, somewhat above room temperature, but strong heat or reflux is not used. B C Br HO O Substitution will not occur at a significant rate. Explanation Check + Х Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibarrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co
- World of ChemistryChemistryISBN:9780618562763Author:Steven S. ZumdahlPublisher:Houghton Mifflin College DivIntroductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning