Ch' 22: Organic Chemistry - PowerPoint PPT Presentation

1 / 14
About This Presentation
Title:

Ch' 22: Organic Chemistry

Description:

each C has 4 atoms bonded to it. all C have tetrahedral arrangement. sp3 hybridization. straight-chained, normal, unbranched hydrocarbons. with no substituent groups ... – PowerPoint PPT presentation

Number of Views:37
Avg rating:3.0/5.0
Slides: 15
Provided by: abi93
Category:

less

Transcript and Presenter's Notes

Title: Ch' 22: Organic Chemistry


1
Ch. 22 Organic Chemistry
  • 22.1 Alkanes

2
Alkanes
  • saturated hydrocarbons
  • only single bonds
  • each C has 4 atoms bonded to it
  • all C have tetrahedral arrangement
  • sp3 hybridization
  • straight-chained, normal, unbranched hydrocarbons
  • with no substituent groups
  • are long chain alkanes

3
Alkanes
  • really a zigzag shape because of 109.5 in C-C-C
    bond
  • structural isomers-
  • different molecules with same atoms (formula)
  • different bonding
  • have different properties

C4H10
C4H10
4
Naming
  • Find the longest chain of carbons
  • count the number and find the prefix
  • name is prefix and ane ending for alkanes
  • If there are substituent groups, number the
    carbons in the chain from one end to the other
  • make the s for groups as small as can
  • Name the groups by taking the prefix for the
    number of carbons in the group and add -yl

5
Naming
  • the positions of each group are given by the s
    of the carbon they are attached to
  • put hyphen between and group and a comma
    between s
  • For more than 1 group, list then in alphabetical
    order
  • add prefix (di, tri, etc) if there are more than
    one of the same type

6
Practice Naming
  • longest chain is 3
  • name propane
  • 1 C group methyl group
  • off of 2 carbon
  • 2-methylpropane
  • longest chain is 3
  • 2- methyl groups
  • 2,2-dimethylpropane

7
Practice Naming
8
Reactions with Alkanes
  • fairly unreactive
  • combustion
  • always added to O2
  • always makes CO2 and H2O
  • substitution
  • when a halogen is added to it, one halogen may
    replace one hydrogen
  • CH4 Cl2 ? CH3Cl HCl
  • dehydrogenation
  • 2H atom are removed to form unsaturated
  • CH3CH3 ? CH2CH2 H2

9
Cyclic Alkanes
  • cyclopropane
  • planar unstable
  • cyclobutane
  • planar and unstable
  • cyclopentane
  • planar and stable
  • cyclohexane
  • puckered and stable

10
Unsaturated Alkenes and Alkynes
  • alkenes contain at least one double bond
  • alkynes contain at least one triple bond
  • change the ending of name to ene or yne
  • add a telling the starting position of the
    special bond

11
Unsaturated Alkenes and Alkynes
  • can also have unsaturated rings
  • cyclohexene
  • double bonds prevent rotation
  • cis-trans isomerism
  • cis- identical groups on same side of bond
  • trans identical groups on opp side of bond

12
Reactions Alkenes and Alkynes
  • Addition Reactions
  • Hydrogenation
  • add hydrogen pair to remove special bond
  • CH2CHCH3 H2 ? CH3-CH2-CH3
  • Halogenation
  • add halogen pair to remove special bond
  • CH2CHCH3 Br2 ? CH2Br-CHBr-CH3

13
Aromatic Hydrocarbons
  • cyclic unsaturated hydrocarbons
  • benzene
  • phenyl group when attached to a chain

14
functional groups
Write a Comment
User Comments (0)
About PowerShow.com