Hey, everyone. So in this video, we're going to take a look at lipids. Now, lipids itself comes from the word "lipo," which is Greek in origin, and it means "fat". Now, when we say lipids, we're going to say that they represent hydrocarbons. So, hydrocarbon-based biomolecules that are hydrophobic, which means they'll be insoluble in polar water, and that's because they themselves are non polar. Here, we're going to say that they are very diverse structurally and functionally, and we'll see how lipids can be broken down into various groups. Lipids can be categorized based on the ability to be hydrolyzed to produce smaller molecules. We're going to say here that many lipids contain what we call fatty acids. A fatty acid is just a long unbranched hydrocarbon chain with a carboxylic acid group at the end. If we take a look here at this graph of the types of lipids, we'd see here in the top left corner, this represents a fatty acid. As you can see, it's just a long hydrocarbon chain with a carboxylic acid at the very end. Here, lipids themselves, we basically break it up into things that are hydrolyzable and things that are not. The two broad categories initially will be hydrolyzable and non hydrolyzable. The non hydrolyzable, although their structures are more complex, there's fewer of them to look at. Here we have our eicosanoids, our steroids, and our terpenes. Then, if we look at our hydrolyzable ones, we have our waxes, which are basically an alcohol ester with a fatty acid connected. We have our Glycerolipids, and here, this one can be broken down into our Triacylglycerols, sometimes called our Triglycerides. Here, it's just a glycerol molecule connected to three fatty acid groups. It then could connect to what's here in this purple box, which also connects it to our sphingolipids. Here, our Glycerolipids and our Sphingolipids, they together help to make our Phospholipids. In it, we have our Phosphoglycerides, so again we have our glycerol molecule here, but instead of being connected to three fatty acids, it's only connected to two with the third portion being a phosphate group connected to an amino alcohol. And then here with our sphingomyelins, instead of having a glycerol, we have here our sphingosine connected to a fatty acid, connected again to a phosphate group with an Amino Alcohol. Again, we can see that these groups are pretty diverse and different from each other. They share some similar characteristics, but there are some key differences between them which we'll go over in terms of many of these molecules when it comes to lipids. Alright. So just keep in mind when we're talking about lipids, fatty acids is just a key part of many of them. Not all of them possess it, but many of them do. And when we're talking about lipids, we can break it down into those that are hydrolyzable and those that are not hydrolyzable.
- 1. A Review of General Chemistry5h 5m
- Summary23m
- Intro to Organic Chemistry5m
- Atomic Structure16m
- Wave Function9m
- Molecular Orbitals17m
- Sigma and Pi Bonds9m
- Octet Rule12m
- Bonding Preferences12m
- Formal Charges6m
- Skeletal Structure14m
- Lewis Structure20m
- Condensed Structural Formula15m
- Degrees of Unsaturation15m
- Constitutional Isomers14m
- Resonance Structures46m
- Hybridization23m
- Molecular Geometry16m
- Electronegativity22m
- 2. Molecular Representations1h 14m
- 3. Acids and Bases2h 46m
- 4. Alkanes and Cycloalkanes4h 19m
- IUPAC Naming29m
- Alkyl Groups13m
- Naming Cycloalkanes10m
- Naming Bicyclic Compounds10m
- Naming Alkyl Halides7m
- Naming Alkenes3m
- Naming Alcohols8m
- Naming Amines15m
- Cis vs Trans21m
- Conformational Isomers13m
- Newman Projections14m
- Drawing Newman Projections16m
- Barrier To Rotation7m
- Ring Strain8m
- Axial vs Equatorial7m
- Cis vs Trans Conformations4m
- Equatorial Preference14m
- Chair Flip9m
- Calculating Energy Difference Between Chair Conformations17m
- A-Values17m
- Decalin7m
- 5. Chirality3h 39m
- Constitutional Isomers vs. Stereoisomers9m
- Chirality12m
- Test 1:Plane of Symmetry7m
- Test 2:Stereocenter Test17m
- R and S Configuration43m
- Enantiomers vs. Diastereomers13m
- Atropisomers9m
- Meso Compound12m
- Test 3:Disubstituted Cycloalkanes13m
- What is the Relationship Between Isomers?16m
- Fischer Projection10m
- R and S of Fischer Projections7m
- Optical Activity5m
- Enantiomeric Excess20m
- Calculations with Enantiomeric Percentages11m
- Non-Carbon Chiral Centers8m
- 6. Thermodynamics and Kinetics1h 22m
- 7. Substitution Reactions1h 48m
- 8. Elimination Reactions2h 30m
- 9. Alkenes and Alkynes2h 9m
- 10. Addition Reactions3h 18m
- Addition Reaction6m
- Markovnikov5m
- Hydrohalogenation6m
- Acid-Catalyzed Hydration17m
- Oxymercuration15m
- Hydroboration26m
- Hydrogenation6m
- Halogenation6m
- Halohydrin12m
- Carbene12m
- Epoxidation8m
- Epoxide Reactions9m
- Dihydroxylation8m
- Ozonolysis7m
- Ozonolysis Full Mechanism24m
- Oxidative Cleavage3m
- Alkyne Oxidative Cleavage6m
- Alkyne Hydrohalogenation3m
- Alkyne Halogenation2m
- Alkyne Hydration6m
- Alkyne Hydroboration2m
- 11. Radical Reactions1h 58m
- 12. Alcohols, Ethers, Epoxides and Thiols2h 42m
- Alcohol Nomenclature4m
- Naming Ethers6m
- Naming Epoxides18m
- Naming Thiols11m
- Alcohol Synthesis7m
- Leaving Group Conversions - Using HX11m
- Leaving Group Conversions - SOCl2 and PBr313m
- Leaving Group Conversions - Sulfonyl Chlorides7m
- Leaving Group Conversions Summary4m
- Williamson Ether Synthesis3m
- Making Ethers - Alkoxymercuration4m
- Making Ethers - Alcohol Condensation4m
- Making Ethers - Acid-Catalyzed Alkoxylation4m
- Making Ethers - Cumulative Practice10m
- Ether Cleavage8m
- Alcohol Protecting Groups3m
- t-Butyl Ether Protecting Groups5m
- Silyl Ether Protecting Groups10m
- Sharpless Epoxidation9m
- Thiol Reactions6m
- Sulfide Oxidation4m
- 13. Alcohols and Carbonyl Compounds2h 17m
- 14. Synthetic Techniques1h 26m
- 15. Analytical Techniques:IR, NMR, Mass Spect7h 3m
- Purpose of Analytical Techniques5m
- Infrared Spectroscopy16m
- Infrared Spectroscopy Table31m
- IR Spect:Drawing Spectra40m
- IR Spect:Extra Practice26m
- NMR Spectroscopy10m
- 1H NMR:Number of Signals26m
- 1H NMR:Q-Test26m
- 1H NMR:E/Z Diastereoisomerism8m
- H NMR Table24m
- 1H NMR:Spin-Splitting (N + 1) Rule22m
- 1H NMR:Spin-Splitting Simple Tree Diagrams11m
- 1H NMR:Spin-Splitting Complex Tree Diagrams12m
- 1H NMR:Spin-Splitting Patterns8m
- NMR Integration18m
- NMR Practice14m
- Carbon NMR4m
- Structure Determination without Mass Spect47m
- Mass Spectrometry12m
- Mass Spect:Fragmentation28m
- Mass Spect:Isotopes27m
- 16. Conjugated Systems6h 13m
- Conjugation Chemistry13m
- Stability of Conjugated Intermediates4m
- Allylic Halogenation12m
- Reactions at the Allylic Position39m
- Conjugated Hydrohalogenation (1,2 vs 1,4 addition)26m
- Diels-Alder Reaction9m
- Diels-Alder Forming Bridged Products11m
- Diels-Alder Retrosynthesis8m
- Molecular Orbital Theory9m
- Drawing Atomic Orbitals6m
- Drawing Molecular Orbitals17m
- HOMO LUMO4m
- Orbital Diagram:3-atoms- Allylic Ions13m
- Orbital Diagram:4-atoms- 1,3-butadiene11m
- Orbital Diagram:5-atoms- Allylic Ions10m
- Orbital Diagram:6-atoms- 1,3,5-hexatriene13m
- Orbital Diagram:Excited States4m
- Pericyclic Reaction10m
- Thermal Cycloaddition Reactions26m
- Photochemical Cycloaddition Reactions26m
- Thermal Electrocyclic Reactions14m
- Photochemical Electrocyclic Reactions10m
- Cumulative Electrocyclic Problems25m
- Sigmatropic Rearrangement17m
- Cope Rearrangement9m
- Claisen Rearrangement15m
- 17. Ultraviolet Spectroscopy51m
- 18. Aromaticity2h 34m
- 19. Reactions of Aromatics: EAS and Beyond5h 1m
- Electrophilic Aromatic Substitution9m
- Benzene Reactions11m
- EAS:Halogenation Mechanism6m
- EAS:Nitration Mechanism9m
- EAS:Friedel-Crafts Alkylation Mechanism6m
- EAS:Friedel-Crafts Acylation Mechanism5m
- EAS:Any Carbocation Mechanism7m
- Electron Withdrawing Groups22m
- EAS:Ortho vs. Para Positions4m
- Acylation of Aniline9m
- Limitations of Friedel-Crafts Alkyation19m
- Advantages of Friedel-Crafts Acylation6m
- Blocking Groups - Sulfonic Acid12m
- EAS:Synergistic and Competitive Groups13m
- Side-Chain Halogenation6m
- Side-Chain Oxidation4m
- Reactions at Benzylic Positions31m
- Birch Reduction10m
- EAS:Sequence Groups4m
- EAS:Retrosynthesis29m
- Diazo Replacement Reactions6m
- Diazo Sequence Groups5m
- Diazo Retrosynthesis13m
- Nucleophilic Aromatic Substitution28m
- Benzyne16m
- 20. Phenols55m
- 21. Aldehydes and Ketones: Nucleophilic Addition4h 56m
- Naming Aldehydes8m
- Naming Ketones7m
- Oxidizing and Reducing Agents9m
- Oxidation of Alcohols28m
- Ozonolysis7m
- DIBAL5m
- Alkyne Hydration9m
- Nucleophilic Addition8m
- Cyanohydrin11m
- Organometallics on Ketones19m
- Overview of Nucleophilic Addition of Solvents13m
- Hydrates6m
- Hemiacetal9m
- Acetal12m
- Acetal Protecting Group16m
- Thioacetal6m
- Imine vs Enamine15m
- Addition of Amine Derivatives5m
- Wolff Kishner Reduction7m
- Baeyer-Villiger Oxidation39m
- Acid Chloride to Ketone7m
- Nitrile to Ketone9m
- Wittig Reaction18m
- Ketone and Aldehyde Synthesis Reactions14m
- 22. Carboxylic Acid Derivatives: NAS2h 51m
- Carboxylic Acid Derivatives7m
- Naming Carboxylic Acids9m
- Diacid Nomenclature6m
- Naming Esters5m
- Naming Nitriles3m
- Acid Chloride Nomenclature5m
- Naming Anhydrides7m
- Naming Amides5m
- Nucleophilic Acyl Substitution18m
- Carboxylic Acid to Acid Chloride6m
- Fischer Esterification5m
- Acid-Catalyzed Ester Hydrolysis4m
- Saponification3m
- Transesterification5m
- Lactones, Lactams and Cyclization Reactions10m
- Carboxylation5m
- Decarboxylation Mechanism14m
- Review of Nitriles46m
- 23. The Chemistry of Thioesters, Phophate Ester and Phosphate Anhydrides1h 10m
- 24. Enolate Chemistry: Reactions at the Alpha-Carbon1h 53m
- Tautomerization9m
- Tautomers of Dicarbonyl Compounds6m
- Enolate4m
- Acid-Catalyzed Alpha-Halogentation4m
- Base-Catalyzed Alpha-Halogentation3m
- Haloform Reaction8m
- Hell-Volhard-Zelinski Reaction3m
- Overview of Alpha-Alkylations and Acylations5m
- Enolate Alkylation and Acylation12m
- Enamine Alkylation and Acylation16m
- Beta-Dicarbonyl Synthesis Pathway7m
- Acetoacetic Ester Synthesis13m
- Malonic Ester Synthesis15m
- 25. Condensation Chemistry2h 9m
- 26. Amines1h 43m
- 27. Heterocycles2h 0m
- Nomenclature of Heterocycles15m
- Acid-Base Properties of Nitrogen Heterocycles10m
- Reactions of Pyrrole, Furan, and Thiophene13m
- Directing Effects in Substituted Pyrroles, Furans, and Thiophenes16m
- Addition Reactions of Furan8m
- EAS Reactions of Pyridine17m
- SNAr Reactions of Pyridine18m
- Side-Chain Reactions of Substituted Pyridines20m
- 28. Carbohydrates5h 53m
- Monosaccharide20m
- Monosaccharides - D and L Isomerism9m
- Monosaccharides - Drawing Fischer Projections18m
- Monosaccharides - Common Structures6m
- Monosaccharides - Forming Cyclic Hemiacetals12m
- Monosaccharides - Cyclization18m
- Monosaccharides - Haworth Projections13m
- Mutarotation11m
- Epimerization9m
- Monosaccharides - Aldose-Ketose Rearrangement8m
- Monosaccharides - Alkylation10m
- Monosaccharides - Acylation7m
- Glycoside6m
- Monosaccharides - N-Glycosides18m
- Monosaccharides - Reduction (Alditols)12m
- Monosaccharides - Weak Oxidation (Aldonic Acid)7m
- Reducing Sugars23m
- Monosaccharides - Strong Oxidation (Aldaric Acid)11m
- Monosaccharides - Oxidative Cleavage27m
- Monosaccharides - Osazones10m
- Monosaccharides - Kiliani-Fischer23m
- Monosaccharides - Wohl Degradation12m
- Monosaccharides - Ruff Degradation12m
- Disaccharide30m
- Polysaccharide11m
- 29. Amino Acids3h 20m
- Proteins and Amino Acids19m
- L and D Amino Acids14m
- Polar Amino Acids14m
- Amino Acid Chart18m
- Acid-Base Properties of Amino Acids33m
- Isoelectric Point14m
- Amino Acid Synthesis: HVZ Method12m
- Synthesis of Amino Acids: Acetamidomalonic Ester Synthesis16m
- Synthesis of Amino Acids: N-Phthalimidomalonic Ester Synthesis13m
- Synthesis of Amino Acids: Strecker Synthesis13m
- Reactions of Amino Acids: Esterification7m
- Reactions of Amino Acids: Acylation3m
- Reactions of Amino Acids: Hydrogenolysis6m
- Reactions of Amino Acids: Ninhydrin Test11m
- 30. Peptides and Proteins2h 42m
- Peptides12m
- Primary Protein Structure4m
- Secondary Protein Structure17m
- Tertiary Protein Structure11m
- Disulfide Bonds17m
- Quaternary Protein Structure10m
- Summary of Protein Structure7m
- Intro to Peptide Sequencing2m
- Peptide Sequencing: Partial Hydrolysis25m
- Peptide Sequencing: Partial Hydrolysis with Cyanogen Bromide7m
- Peptide Sequencing: Edman Degradation28m
- Merrifield Solid-Phase Peptide Synthesis18m
- 31. Catalysis in Organic Reactions1h 30m
- 32. Lipids 2h 50m
- 34. Nucleic Acids1h 32m
- 35. Transition Metals5h 33m
- Electron Configuration of Elements45m
- Coordination Complexes20m
- Ligands24m
- Electron Counting10m
- The 18 and 16 Electron Rule13m
- Cross-Coupling General Reactions40m
- Heck Reaction40m
- Stille Reaction13m
- Suzuki Reaction25m
- Sonogashira Coupling Reaction17m
- Fukuyama Coupling Reaction15m
- Kumada Coupling Reaction13m
- Negishi Coupling Reaction16m
- Buchwald-Hartwig Amination Reaction19m
- Eglinton Reaction17m
- 36. Synthetic Polymers1h 49m
- Introduction to Polymers6m
- Chain-Growth Polymers10m
- Radical Polymerization15m
- Cationic Polymerization8m
- Anionic Polymerization8m
- Polymer Stereochemistry3m
- Ziegler-Natta Polymerization4m
- Copolymers6m
- Step-Growth Polymers11m
- Step-Growth Polymers: Urethane6m
- Step-Growth Polymers: Polyurethane Mechanism10m
- Step-Growth Polymers: Epoxy Resin8m
- Polymers Structure and Properties8m
Intro to Lipids - Online Tutor, Practice Problems & Exam Prep
Lipids, derived from the Greek word "lipo" meaning fat, are diverse hydrocarbon-based biomolecules that are hydrophobic and insoluble in polar water. They can be categorized into hydrolyzable lipids, like triglycerides and phospholipids, which contain fatty acids, and non-hydrolyzable lipids, such as steroids and terpenes. Key functions of lipids include energy storage, insulation, bio-signaling, and forming cell membrane structures, facilitating nutrient transport and ion passage within biological systems.
Intro to Lipids Concept 1
Video transcript
Intro to Lipids Concept 2
Video transcript
Now remember, we said that lipids can be very diverse structurally and functionally. Here are some primary lipid functions; we have our energy source and storage when it comes to certain types of them. Next, we have insulation and protection. So, this person shivering can be helped by lipids that provide insulation to keep us warm. Next, we have Bio Signaling. We can utilize them to communicate between different biomolecules within a living system. And then finally, we have our cell membrane structure. Some of these diverse forms of lipids form integral parts of different types of cells, in terms of their cell membranes. They help with the transportation of nutrients into the cell and aid in the passage between membranes of ions and different types of helpful components for any biological system. So, these are just some of the main primary functions of a lipid.
Intro to Lipids Example 1
Video transcript
In this example question it asks, which of the following statements about lipids are not true?
Option A: Steroids are a class of lipids which cannot be hydrolyzed by water. Remember when we looked at that graph where we had the two broad groups where lipids are either hydrolyzable or not hydrolyzable, we saw that steroids were indeed in the not hydrolyzable category. So, this statement here is true.
Option B: All lipids are insoluble in non-polar solvents but soluble in polar solvents. Lipids themselves, we said that they are hydrophobic because they are non-polar. Because they're non-polar, they would be soluble in non-polar solvents such as hexanes, but they would be insoluble in solvents like water. Thus, this statement is false, and it is our answer.
Option C: Certain lipids play an important role as components of biological membranes. Yes, when we're talking about our phospholipids, we know that from biology we have a connection between phospholipids and biological membranes, so this is true.
Option D: Lipids contain a large number of non-polar Carbon Hydrogen bonds making them overall non-polar. This is true. Although they possess a polar carboxylic acid end when it comes to fatty acids for those types of lipids, not all lipids have that. Lipids, basically overall, are non-polar because of the large presence of Carbon Hydrogen bonds. So, this statement here is true.
So, out of all our choices, only option B is an incorrect statement and therefore our final answer.
Do you want more practice?
More setsHere’s what students ask on this topic:
What are the main types of lipids and their functions?
Lipids are categorized into hydrolyzable and non-hydrolyzable types. Hydrolyzable lipids include triglycerides, phospholipids, and waxes, which contain fatty acids. Non-hydrolyzable lipids include steroids, terpenes, and eicosanoids. The main functions of lipids are energy storage, insulation and protection, bio-signaling, and forming cell membrane structures. Triglycerides store energy, phospholipids form cell membranes, and steroids like cholesterol are involved in signaling and membrane fluidity. Waxes provide protective coatings, while terpenes and eicosanoids play roles in signaling and metabolic pathways.
How are lipids classified based on their ability to be hydrolyzed?
Lipids are classified into hydrolyzable and non-hydrolyzable categories. Hydrolyzable lipids can be broken down into smaller molecules and include triglycerides, phospholipids, and waxes. These lipids contain fatty acids that can be released through hydrolysis. Non-hydrolyzable lipids, such as steroids, terpenes, and eicosanoids, cannot be broken down into smaller molecules through hydrolysis. These lipids have more complex structures and serve various functions, including signaling and structural roles in cell membranes.
What is the structure of a fatty acid?
A fatty acid is a long, unbranched hydrocarbon chain with a carboxylic acid group at one end. The general structure can be represented as R-COOH, where R is the hydrocarbon chain. The length of the hydrocarbon chain can vary, typically ranging from 4 to 28 carbon atoms. Fatty acids can be saturated, with no double bonds between carbon atoms, or unsaturated, with one or more double bonds. The presence of double bonds affects the physical properties and functions of the fatty acid.
What roles do lipids play in cell membrane structure?
Lipids, particularly phospholipids, play crucial roles in cell membrane structure. Phospholipids form a bilayer, with hydrophobic tails facing inward and hydrophilic heads facing outward, creating a semi-permeable membrane. This bilayer structure allows for the selective transport of nutrients and ions into and out of the cell. Additionally, cholesterol, a type of steroid lipid, is embedded within the membrane, contributing to membrane fluidity and stability. Sphingolipids also play a role in cell signaling and membrane structure.
What are the primary functions of lipids in biological systems?
Lipids serve several primary functions in biological systems. They act as energy storage molecules, with triglycerides storing energy in adipose tissue. Lipids provide insulation and protection, helping to maintain body temperature and protect organs. They are involved in bio-signaling, with molecules like steroids and eicosanoids participating in cellular communication. Additionally, lipids are essential components of cell membranes, forming the lipid bilayer that regulates the passage of substances into and out of cells and maintaining membrane integrity.