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Molecules of Life

Molecules of Life. Introduction to organic compounds. Organic Compounds – compounds that contain carbon Hydrocarbons – compounds composed of only hydrogen and carbon. Length. Prefixes. Bonding. Double and triple bonding do occur within hydrocarbons

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Molecules of Life

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  1. Molecules of Life

  2. Introduction to organic compounds • Organic Compounds – compounds that contain carbon • Hydrocarbons – compounds composed of only hydrogen and carbon

  3. Length

  4. Prefixes

  5. Bonding • Double and triple bonding do occur within hydrocarbons • Notice what the bonding does to the amount of hydrogens attached to that carbon

  6. Rings

  7. Isomers • Same formula but different structural arrangement

  8. Review • Identify the following hydrocarbons

  9. Bell Ringer • Please give the molecular formula and draw the molecular structurer of the following compounds • Ethane • Cyclopropane

  10. Functional Groups • Chemical groups that effect a molecule’s function by participation in chemical reactions

  11. Amino Acid

  12. Warm up Question • What are some examples of things that are complex yet made up of simple units.

  13. Four Categories of Macromolecules Macromolecule- a molecule containing a very large number of atoms. • Carbohydrates • Lipids • Proteins • Nucleic acids

  14. Macromolecules • Polymer – large molecule consisting of identical or similar building blocks strung together • Monomer – building blocks of polymers

  15. Macromolecules • Dehydration synthesis – removes an –H from one monomer and an –OH from another to form a polymer and water • Hydrolysis – Polymer is broken apart with the addition of water

  16. Macromolecules • Both dehydration synthesis and hydrolysis require enzymes • Enzymes= specialized proteins that speed up a chemical reaction

  17. Bell Ringer • What are the products formed after a dehydration synthesis reaction? In the picture below identify the water molecules that will leave to clear up space for the bond to form between our polymer and our monomer.

  18. Carbohydrates • Monosaccharide – the carbohydrate monomer • General formula: CnH2nOn • May have 3 to 7 carbons • Glucose, Fructose, and Ribose • May form rings in aqueous solutions

  19. Disaccharide • 2 monosaccharides linked by dehydration synthesis • - Glycosidic linkage

  20. Bell Ringer • What are the products formed after a dehydration synthesis reaction? • What is the monomer of carbohydrates called? • What is the structure called when 2 monosaccharides are connected.

  21. Disaccharide • Glucose + Glucose = Maltose • Glucose + Fructose = Sucrose • Glucose + Galactose = Lactose Maltose Sucrose Lactose

  22. Polysaccharides • Hundreds to thousands of monosaccharides linked together by dehydration synthesis • Starch – storage polysaccharide in plants made of glucose

  23. Polysaccharides • Glycogen – storage polysaccharide in animals made of glucose

  24. Polysaccharides • Cellulose – structural component of plants

  25. Polysaccharides • Chitin – structural polysaccharide in animals • Exoskeleton of insects

  26. Bell Ringer • Have your homework out so we can review the questions. • What are the the two polysaccharides used for structure?

  27. Lipids • Mostly hydrogen and carbon • Hydrophobic – water-fearing • They are neither large molecules or polymers

  28. Fats • Dehydration synthesis links a glycerol to 3 fatty acids to form a triglyceride

  29. Fats • Saturated fats – hydrocarbon chains that have the maximum number of hydrogen atoms (all single bonds) • Example – Animal fats (solid at room temperature)

  30. Fats • Unsaturated fats – has at least one double bond • Example – Plant fats (liquid at room temperature)

  31. Fats • Function: Long term energy storage

  32. Bell Ringer • What is the difference between saturated and unsaturated fats? • What does hydrophobic and hydrophilic mean? • Are fats/ lipids hydrophilic or hydrophobic? 3

  33. Phospholipids • Function: Major component of cell membranes • Organic phosphate linked to 2 fatty acid chains by a glycerol • Phosphate head is hydrophilic • Fatty acid tail is hydrophobic

  34. Waxes • Very hydrophobic • Mostly hydrocarbon chains

  35. Steroids • Four fused carbon rings • Example: Cholesterol – used in cell membrane and the starting material of testosterone and estrogen

  36. Testosterone and estrogen

  37. Building Lipids • Fatty Acid Glycerol

  38. Building Lipids • Fatty Acid Glycerol

  39. Building Lipids • Fatty Acid Glycerol

  40. Bell Ringer • What parts of our phospholipid are considered hydrophobic and hydrophilic? • What are the defining features of a steroid?

  41. Protein Structure • Monomer – Amino Acid Amino group Carboxyl group Side chain

  42. Protein Structure • There are 20 different amino acids; each with a different side chain (R group) • Some amino acids are hydrophilic, some are hydrophobic

  43. Dipeptides • Dehydration synthesis links together 2 amino acids and forms a dipeptide (held together by peptide bond)

  44. Polypeptides • Many amino acids = polypeptide

  45. Carb vs Proteins

  46. Protein Structure • Primary- unique sequence amino acids

  47. Protein Structure • Secondary – parts of the polypeptide coils or folds into patterns • Alpha helix and beta pleated sheets • Patterns are maintained by hydrogen bonds

  48. Protein Structure • Tertiary – 3D shape of a polypeptide • R groups are involved in creating the protein’s shape

  49. Protein Structure • Quaternary – 2 or more polypeptide subunits

  50. Protein Shape • Denaturation – polypeptide chains unravel, losing their shape and, consequently, their function • Caused by excessive heat, pH, or salt concentration

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