Multiple Choice
Draw a cephalin with stearic acid at C1 and oleic acid at C2.
Table of contents
- 1. Matter and Measurements4h 31m
- What is Chemistry?7m
- The Scientific Method9m
- Classification of Matter16m
- States of Matter8m
- Physical & Chemical Changes19m
- Chemical Properties8m
- Physical Properties5m
- Intensive vs. Extensive Properties13m
- Temperature (Simplified)9m
- Scientific Notation13m
- SI Units (Simplified)5m
- Metric Prefixes24m
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- Dimensional Analysis22m
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- 2. Atoms and the Periodic Table5h 23m
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- Subatomic Particles (Simplified)12m
- Isotopes17m
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- Atomic Mass (Simplified)17m
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- Ions and the Octet Rule9m
- Ions and the Octet Rule (Simplified)8m
- Valence Electrons of Elements (Simplified)5m
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- 3. Ionic Compounds2h 18m
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- Naming Monoatomic Cations6m
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- Multiple Bonds4m
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- Lewis Dot Structures: Ions (Simplified)8m
- Lewis Dot Structures: Exceptions (Simplified)12m
- Resonance Structures (Simplified)5m
- Valence Shell Electron Pair Repulsion Theory (Simplified)4m
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- Molecular Geometry (Simplified)11m
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- 5. Classification & Balancing of Chemical Reactions3h 17m
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- Law of Conservation of Mass5m
- Balancing Chemical Equations (Simplified)13m
- Solubility Rules16m
- Molecular Equations18m
- Types of Chemical Reactions12m
- Complete Ionic Equations18m
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- Redox Reactions17m
- Spontaneous Redox Reactions8m
- Balancing Redox Reactions: Acidic Solutions17m
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- Solutions6m
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- Strong Acid Strong Base Titrations (Simplified)10m
- 11. Nuclear Chemistry56m
- BONUS: Lab Techniques and Procedures1h 38m
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- 12. Introduction to Organic Chemistry1h 34m
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- 18. Amino Acids and Proteins1h 51m
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- 20. Carbohydrates1h 41m
- Intro to Carbohydrates4m
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- D vs L Enantiomers8m
- Cyclic Hemiacetals8m
- Intro to Haworth Projections4m
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- Mutarotation4m
- Reduction of Monosaccharides10m
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- Glycosidic Linkage14m
- Disaccharides7m
- Polysaccharides2m
- 21. The Generation of Biochemical Energy2h 8m
- 22. Carbohydrate Metabolism2h 22m
- 23. Lipids2h 26m
- Intro to Lipids6m
- Fatty Acids25m
- Physical Properties of Fatty Acids6m
- Waxes4m
- Triacylglycerols12m
- Triacylglycerol Reactions: Hydrogenation8m
- Triacylglycerol Reactions: Hydrolysis13m
- Triacylglycerol Reactions: Oxidation7m
- Glycerophospholipids15m
- Sphingomyelins13m
- Steroids15m
- Cell Membranes7m
- Membrane Transport10m
- 24. Lipid Metabolism1h 45m
- 25. Protein and Amino Acid Metabolism1h 37m
- 26. Nucleic Acids and Protein Synthesis2h 54m
- Intro to Nucleic Acids4m
- Nitrogenous Bases16m
- Nucleoside and Nucleotide Formation9m
- Naming Nucleosides and Nucleotides13m
- Phosphodiester Bond Formation7m
- Primary Structure of Nucleic Acids11m
- Base Pairing10m
- DNA Double Helix6m
- Intro to DNA Replication20m
- Steps of DNA Replication11m
- Types of RNA10m
- Overview of Protein Synthesis4m
- Transcription: mRNA Synthesis9m
- Processing of pre-mRNA5m
- The Genetic Code6m
- Introduction to Translation7m
- Translation: Protein Synthesis18m
23. Lipids
Glycerophospholipids
Struggling with GOB Chemistry?
Join thousands of students who trust us to help them ace their exams!Watch the first videoMultiple Choice
Draw a glycerophospholipid with lauric acid at C1, myristic acid at C2, and choline bonded to phosphate.
A
B
C
D
Verified step by step guidance1
Identify the structure of a glycerophospholipid, which consists of a glycerol backbone, two fatty acid chains, a phosphate group, and an alcohol group attached to the phosphate.
Recognize that lauric acid is a 12-carbon saturated fatty acid and should be attached to the C1 position of the glycerol backbone.
Recognize that myristic acid is a 14-carbon saturated fatty acid and should be attached to the C2 position of the glycerol backbone.
Understand that choline is a quaternary ammonium compound that should be bonded to the phosphate group, forming a phosphatidylcholine.
Draw the glycerophospholipid structure by placing lauric acid at C1, myristic acid at C2, and choline bonded to the phosphate group, ensuring the correct connectivity and orientation of each component.
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