Interpretation:
The reason for micelle formation by the soap molecules to suspend greasy dirt in a solution needs to be explained.
Concept introduction:
A micelle is a type of structure that is formed when different molecules such as soaps and detergents are mixed with water. The molecule contains fatty acid, a salt of fatty acid, phospholipids, or other similar types of compounds.
Answer to Problem 41A
The micelle is an aggregated form of surfactant in liquid to form a colloidal suspension.
The hydrophobic part of the soap is towards the dirt part and the hydrophilic part projects outside in the bristle’s manner.
Explanation of Solution
A micelle is a composition of surfactant molecules scattered in a liquid that is a colloid. A complete micelle form in an aqueous solution having two phases one is hydrophilic and the other one is hydrophobic. The hydrophilic head regions in contact withthe solvent, and attached hydrophobic single tail regions in the central side of the micelle.
The greasy dirt is present at the center of the micelle and surrounded by the hydrophobic part. It combines with the dirt and hydrophilic part dissolved in the water to rinse out the dirt.
The molecules of soap arrange in a rounded shape in micelle formation and it covers the dirt at the center part of the cluster. The formed micelles are remain suspended in the water resulting a colloidal solution. The hydrophobic ends attached to dirt and washout with water.
Chapter 21 Solutions
World of Chemistry, 3rd edition
- Please correct answer and don't used hand raitingarrow_forwardPlease correct answer and don't used hand raitingarrow_forward(a) The following synthesis of the molecule shown in the circle has a major problem. What is this problem? (2 pts) 1) HBr (no peroxides) 2) H- NaNH2 Br 3) NaNH, 4) CH3Br 5) H2, Pd (b) Starting with the molecule shown below and any other materials with two carbons or less, write out an alternate synthesis of the circled molecule. More than one step is needed. Indicate the reagent(s) and the major product in all the steps in your synthesis. (5 pts) 2024 Fall Term (1) Organic Chemistry 1 (Lec) CHEM 22204 02[6386] (Hunter College) (c) Using the same starting material as in part (b) and any other materials win two carpons or less, write out syntheses of the circled molecules shown below. More than one step is needed in each case. Indicate the reagent(s) and the major product in all the steps in your synthesis. You may use reactions and products from your synthesis in part (b). (5 pts)arrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY