Organic Chemistry
8th Edition
ISBN: 9781305580350
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 26, Problem 26.27P
Interpretation Introduction
Interpretation:
The hydrophobic and hydrophilic regions of a phospholipid have to be identified.
Concept-Introduction:
Hydrophobic:
- Hydrophobic means repelling of water molecules. Hydrophobic molecules are insoluble in water and non-polar in nature.
- Due to its non-solvation, hydrophobic molecules aggregate in polar solvents like water.
- This aggregation of hydrophobic molecules leads to membrane formation, surfactant action, protein folding, and protein-protein recognition.
Hydrophilic:
Hydrophilic molecules tend to attract water molecules. These are water soluble and mostly polar in nature.
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
What is the difference between lyophobic sol and lyophilic sol?
Describe the basic structure of phospholipids and glycolipids. What functions do these lipids have in living organisms?
11
Chapter 26 Solutions
Organic Chemistry
Ch. 26.1 - Prob. 26.1PCh. 26.6 - Prob. AQCh. 26.6 - Prob. BQCh. 26.6 - Prob. CQCh. 26.6 - Prob. DQCh. 26.6 - Prob. FQCh. 26 - Prob. 26.2PCh. 26 - Identify the hydrophobic and hydrophilic region(s)...Ch. 26 - Prob. 26.4PCh. 26 - Prob. 26.5P
Ch. 26 - Prob. 26.6PCh. 26 - Prob. 26.7PCh. 26 - Prob. 26.8PCh. 26 - Prob. 26.9PCh. 26 - How many moles of H2 are used in the catalytic...Ch. 26 - Prob. 26.11PCh. 26 - Prob. 26.12PCh. 26 - Prob. 26.13PCh. 26 - Prob. 26.14PCh. 26 - Prob. 26.15PCh. 26 - Prob. 26.16PCh. 26 - Prob. 26.17PCh. 26 - Prob. 26.18PCh. 26 - Prob. 26.20PCh. 26 - Prob. 26.21PCh. 26 - Prob. 26.22PCh. 26 - Prob. 26.23PCh. 26 - Following is a structural formula for cortisol...Ch. 26 - Prob. 26.25PCh. 26 - Draw the structural formula of a lecithin...Ch. 26 - Prob. 26.27PCh. 26 - Prob. 26.28PCh. 26 - Prob. 26.29PCh. 26 - Prob. 26.30PCh. 26 - Prob. 26.31PCh. 26 - Prob. 26.32PCh. 26 - Prob. 26.33P
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- 2. Draw the skeletal carbon structure of triacylglycerol and highlight the ester linkage.arrow_forwardPart 4 - Lipids The cow milk B-lactoglobulin protein can bind to several lipids among which myristic acid, palmitic acid, stearic acid, and oleic acid. Question 4-1 b) Draw the semi-developed formula of both the palmitic acid and the oleic acid at physiological pH. Circle the hydrophilic part of each molecule. Do not forget to number the carbon atoms.arrow_forwardWhat happens if glycerol reacts with acetyl chloride in the formation of esters?arrow_forward
- Which of the following is not true of a lipid? They are composed of both hydrophobic and hydrophilic components. They can contain both sp2 hybridised and sp3 hybridised carbon atoms. They are always long and linear molecules. The primary biological functions of lipids include energy storage, signalling and functioning as structural components of cell membranes. They are important biomolecules for life.arrow_forwardCompare the strength of intermolecular forces in straight and branched-chain organic compounds.arrow_forwardWhat is produced from triacylglycerol that forms a mixture of long chain carboxylate salts?arrow_forward
- Why do fatty acid esters (the biodiesel) and glycerin separate into different layers?arrow_forward4. Write the two chemical equations that show the titration reactions of the carboxylic acid group and the protonated amino group of glycylglycine with sodium hydroxide.arrow_forwardWhich of the terms characterize compounds with significant solubility in the water phase? i) lipophilic ii)hydrophobic iii)hydrophilic iv) lipophobicarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningIntroductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage LearningChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
- Chemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,