
Concept explainers
(a)
Interpretation:
Hydrophilic head group and hydrophobic tail in hexadecyltrimethylammonium chloride is to be identified.
Concept introduction:
Cationic detergents are the detergents in which the active part of the molecule is a positive ion (cation). Cationic detergents are usually quaternary ammonium salts.
The ionic group in a detergent is the hydrophilic head group, and the nonpolar part of the detergent is the hydrophobic tail group.
(b)
Interpretation:
Micelle that would form, if the compound was dissolved in water, is to be drawn.
Concept introduction:
Detergents are long-chain molecules that are ionic on one end and highly non-polar on the other end. Detergents are dissolved in water as micelles, in which, the ionic head group is arranged on the exterior, and the hydrocarbon (non-polar) tails are arranged on the interior.
(c)
Interpretation:
Intermolecular forces that are primarily responsible for the solubility of micelles in water is to be determined.
Concept introduction:
In a micelle, the nonpolar tails are on the inside of the sphere, where they can interact with one another via extensive induced dipole–induced dipole interactions, whereas the cationic groups, that is, positively charged head groups are on the outside, where they can form the greatest number of ion–dipole interactions with the surrounding water molecules.

Trending nowThis is a popular solution!

Chapter 2 Solutions
Organic Chemistry: Principles And Mechanisms
- Synthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIf possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forward
- Synthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIndicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forwardWe mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forward
- Indicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forwardIndicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forwardIndicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forward
- Question 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forwardIndicate the products obtained if 2,2-dimethylpropanal and acetaldehyde are mixed with sodium ethoxide in ethanol.arrow_forwardIndicate the products obtained if 2,2-dimethylpropanal and acetaldehyde are reacted with sodium ethoxide in ethanol.arrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
- Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning





