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Soap bubbles form because fatty acid salts organize into: (A) lysosomes. (B) micelles. (C) phospholipid bilayers. (D) hydrogen bonds.

Short Answer

Expert verified
(B) micelles

Step by step solution

01

Understand the components

Identify the key term in the question: 'fatty acid salts.' These are compounds that have both hydrophobic (water-repelling) and hydrophilic (water-attracting) parts.
02

Recognize the behavior of fatty acid salts in water

In water, the hydrophobic tails of fatty acid salts avoid water and interact with each other, while the hydrophilic heads interact with the water.
03

Identify the structure formed

When fatty acid salts are in an aqueous solution, they tend to form spherical structures where the hydrophobic tails are hidden inside and hydrophilic heads face outward towards the water. This structure is known as a micelle.
04

Evaluate the answer choices

Consider each option: (A) lysosomes are cell organelles, not related to fatty acid salts; (B) micelles accurately describe the structure formed; (C) phospholipid bilayers are part of membrane structure, not spherical; (D) hydrogen bonds are types of chemical bonds, not structures.
05

Select the correct answer

Based on the analysis, the correct answer is (B) micelles.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

micelles
In aqueous solutions, fatty acid salts naturally organize into structures called micelles. These spherical formations occur because fatty acid salts have dual characteristics—hydrophobic tails that repel water and hydrophilic heads that attract water. When introduced to water, the hydrophobic tails of these molecules try to avoid interacting with water and thus, gather in the center of the micelle. The hydrophilic heads, on the other hand, face outward, engaging with the surrounding water molecules. This arrangement minimizes the unfavorable interaction between water and the hydrophobic tails, creating a stable structure.
hydrophobic and hydrophilic interactions
Hydrophobic and hydrophilic interactions play crucial roles in the behavior of molecules in biological chemistry. Hydrophobic molecules, like the tails of fatty acids, do not mix well with water. They tend to clump together to minimize their exposure to water. Conversely, hydrophilic molecules, such as the heads of fatty acids, are attracted to water and interact favorably with it. These interactions are fundamental in the formation of structures like micelles:
  • Hydrophobic tails stay inside the micelle, away from water.
  • Hydrophilic heads face the water, making the structure stable.
This dynamic is essential for understanding why soap bubbles and other similar structures form.
aqueous solutions
Aqueous solutions are simply solutions where water is the solvent. Many chemical reactions and interactions in biological systems occur in aqueous solutions. When substances like fatty acid salts are placed in water, their hydrophilic and hydrophobic parts behave differently:
  • Hydrophilic parts dissolve well and interact with water molecules.
  • Hydrophobic parts do not dissolve, leading to the formation of structured arrangements like micelles.
Understanding these behaviors is crucial for studying various biological and chemical processes, as water is the most common solvent in biological systems.
biological chemistry
Biological chemistry focuses on chemical processes within and relating to living organisms. It explains how molecules like fatty acid salts behave in environments such as the human body, largely composed of water. Knowing how hydrophobic and hydrophilic interactions work helps in understanding cellular processes and the formation of structures like membranes and micelles. For instance:
  • Fatty acids form the basic components of cell membranes.
  • Hydrophilic heads face the watery cell exterior and interior, while hydrophobic tails remain inside.
This knowledge is fundamental in fields like biochemistry and molecular biology.

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Most popular questions from this chapter

Which of the following is/are true about sphingolipids? I. They are all phospholipids. II. They all contain a sphingosine backbone. III. They can have either phosphodiester or glycosidic linkages to their polar head groups. (A) I only (B) III only (C) II and III only (D) I, II, and III

Which of the following statements about saturation is FALSE? (A) \(\quad\) It can describe the number of double or triple bonds in a fatty acid tail. (B) \(\quad\) It determines at least one of the properties of membranes. (C) \(\quad\) More saturated fatty acids make for a more fluid solution. (D) \(\quad\) Fully saturated fatty acids have only single bonds.

Which of the following best describes the structure of steroids? (A) Three cyclopentane rings, one cyclohexane ring (B) Three cyclohexane rings, one cyclopentane ring (C) Four carbon rings, differing in structure for each steroid (D) Three cyclic carbon rings and a functional group

Which of the following is true of amphipathic molecules? (A) \(\quad\) They form protective spheres in any solvent, with hydrophobic molecules interior and hydrophilic molecules exterior. (B) \(\quad\) They have two fatty acid chains and a polar head group. (C) \(\quad\) They are important to the formation of the phospholipid bilayer and soap bubbles. (D) \(\quad\) They have a glycerol base.

Why are triacylglycerols used in the human body for energy storage? (A) \(\quad\) They are highly hydrated and therefore can store lots of energy. (B) \(\quad\) They always have short fatty acid chains for easy access by metabolic enzymes. (C) \(\quad\) The carbon atoms of the fatty acid chains are highly reduced and therefore yield more energy upon oxidation. (D) \(\quad\) Polysaccharides, which would actually be a better energy storage form, would dissolve in the body.

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