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Chapter 3 Structure and Stereochemistry of Alkanes

Chapter 3. 2. Classification Review. Chapter 3. 3. Alkane Formulas. All C-C single bondsSaturated with hydrogensRatio: CnH2n 2Alkane homologs: CH3(CH2)nCH3Same ratio for branched alkanes. =>. Chapter 3. 4. Common Names. Isobutane,

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Chapter 3 Structure and Stereochemistry of Alkanes

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    1. Chapter 3 Structure and Stereochemistry of Alkanes

    2. Chapter 3 2 Classification Review

    3. Chapter 3 3 Alkane Formulas All C-C single bonds Saturated with hydrogens Ratio: CnH2n+2 Alkane homologs: CH3(CH2)nCH3 Same ratio for branched alkanes

    4. Chapter 3 4 Common Names Isobutane, isomer of butane Isopentane, isohexane, etc., methyl branch on next-to-last carbon in chain. Neopentane, most highly branched Five possible isomers of hexane, 18 isomers of octane and 75 for decane! =>

    5. Chapter 3 5 Alkane Examples

    6. Chapter 3 6 IUPAC Names Find the longest continuous carbon chain. Number the carbons, starting closest to the first branch. Name the groups attached to the chain, using the carbon number as the locator. Alphabetize substituents. Use di-, tri-, etc., for multiples of same substituent. =>

    7. Chapter 3 7 Longest Chain The number of carbons in the longest chain determines the base name: ethane, hexane. (Listed in Table 3.2, page 82.) If there are two possible chains with the same number of carbons, use the chain with the most substituents.

    8. Chapter 3 8 Number the Carbons Start at the end closest to the first attached group. If two substituents are equidistant, look for the next closest group.

    9. Chapter 3 9 Name Alkyl Groups CH3-, methyl CH3CH2-, ethyl CH3CH2CH2-, n-propyl CH3CH2CH2CH2-, n-butyl

    10. Chapter 3 10 Propyl Groups

    11. Chapter 3 11 Butyl Groups

    12. Chapter 3 12 Isobutyl Groups

    13. Chapter 3 13 Alphabetize Alphabetize substituents by name. Ignore di-, tri-, etc. for alphabetizing.

    14. Chapter 3 14 Complex Substituents If the branch has a branch, number the carbons from the point of attachment. Name the branch off the branch using a locator number. Parentheses are used around the complex branch name.

    15. Chapter 3 15 Physical Properties Solubility: hydrophobic Density: less than 1 g/mL Boiling points increase with increasing carbons (little less for branched chains).

    16. Chapter 3 16 Boiling Points of Alkanes

    17. Chapter 3 17 Melting Points of Alkanes

    18. Chapter 3 18 Branched Alkanes Lower b.p. with increased branching Higher m.p. with increased branching Examples:

    19. Chapter 3 19 Major Uses of Alkanes C1-C2: gases (natural gas) C3-C4: liquified petroleum (LPG) C5-C8: gasoline C9-C16: diesel, kerosene, jet fuel C17-up: lubricating oils, heating oil Origin: petroleum refining =>

    20. Chapter 3 20 Reactions of Alkanes Combustion

    21. Chapter 3 21 Conformers of Alkanes Structures resulting from the free rotation of a C-C single bond May differ in energy. The lowest-energy conformer is most prevalent. Molecules constantly rotate through all the possible conformations. =>

    22. Chapter 3 22 Ethane Conformers Staggered conformer has lowest energy. Dihedral angle = 60 degrees

    23. Chapter 3 23 Ethane Conformers (2) Eclipsed conformer has highest energy Dihedral angle = 0 degrees

    24. Chapter 3 24 Conformational Analysis Torsional strain: resistance to rotation. For ethane, only 12.6 kJ/mol

    25. Chapter 3 25 Propane Conformers Note slight increase in torsional strain due to the more bulky methyl group.

    26. Chapter 3 26 Butane Conformers C2-C3 Highest energy has methyl groups eclipsed. Steric hindrance Dihedral angle = 0 degrees

    27. Chapter 3 27 Butane Conformers (2) Lowest energy has methyl groups anti. Dihedral angle = 180 degrees

    28. Chapter 3 28 Butane Conformers (3) Methyl groups eclipsed with hydrogens Higher energy than staggered conformer Dihedral angle = 120 degrees

    29. Chapter 3 29 Butane Conformers (4) Gauche, staggered conformer Methyls closer than in anti conformer Dihedral angle = 60 degrees

    30. Chapter 3 30 Conformational Analysis

    31. Chapter 3 31 Higher Alkanes Anti conformation is lowest in energy. Straight chain actually is zigzag.

    32. Chapter 3 32 Cycloalkanes Rings of carbon atoms (-CH2- groups) Formula: CnH2n Nonpolar, insoluble in water Compact shape Melting and boiling points similar to branched alkanes with same number of carbons =>

    33. Chapter 3 33 Naming Cycloalkanes Cycloalkane usually base compound Number carbons in ring if >1 substituent. First in alphabet gets lowest number. May be cycloalkyl attachment to chain.

    34. Chapter 3 34 Cis-Trans Isomerism Cis: like groups on same side of ring Trans: like groups on opposite sides of ring =>

    35. Chapter 3 35 Cycloalkane Stability 5- and 6-membered rings most stable Bond angle closest to 109.5? Angle (Baeyer) strain Measured by heats of combustion per -CH2 - =>

    36. Chapter 3 36 Heats of Combustion/CH2 Alkane + O2 ? CO2 + H2O

    37. Chapter 3 37 Cyclopropane Large ring strain due to angle compression Very reactive, weak bonds

    38. Chapter 3 38 Cyclopropane (2) Torsional strain because of eclipsed hydrogens

    39. Chapter 3 39 Cyclobutane Angle strain due to compression Torsional strain partially relieved by ring-puckering

    40. Chapter 3 40 Cyclopentane If planar, angles would be 108?, but all hydrogens would be eclipsed. Puckered conformer reduces torsional strain.

    41. Chapter 3 41 Cyclohexane Combustion data shows its unstrained. Angles would be 120?, if planar. The chair conformer has 109.5? bond angles and all hydrogens are staggered. No angle strain and no torsional strain. =>

    42. Chapter 3 42 Chair Conformer

    43. Chapter 3 43 Boat Conformer

    44. Chapter 3 44 Conformational Energy

    45. Chapter 3 45 Axial and Equatorial Positions

    46. Chapter 3 46 Monosubstituted Cyclohexanes

    47. Chapter 3 47 1,3-Diaxial Interactions

    48. Chapter 3 48 Disubstituted Cyclohexanes

    49. Chapter 3 49 Cis-Trans Isomers Bonds that are cis, alternate axial-equatorial around the ring.

    50. Chapter 3 50 Bulky Groups Groups like t-butyl cause a large energy difference between the axial and equatorial conformer. Most stable conformer puts t-butyl equatorial regardless of other substituents.

    51. Chapter 3 51 Bicyclic Alkanes Fused rings share two adjacent carbons. Bridged rings share two nonadjacent Cs.

    52. Chapter 3 52 Cis- and Trans-Decalin Fused cyclohexane chair conformers Bridgehead Hs cis, structure more flexible Bridgehead Hs trans, no ring flip possible.

    53. Chapter 3 53 Bicyclo[4.4.0]decane

    54. Chapter 3 54

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