Organic Compounds: Alkanes and Their Stereochemistry: Based On Mcmurry'S Organic Chemistry, 7 Edition

3.
Organic Compounds:
Alkanes and Their
Stereochemistry
Based on McMurry’s Organic Chemistry, 7th edition

Why this Chapter
 Alkanes are unreactive, but provide useful vehicle to
introduce important ideas about organic compounds
 Alkanes will be used to discuss basic approaches to naming

organic compounds
 We will take an initial look at 3-D aspects of molecules
2
3.1 Functional Groups
 Functional group -
collection of atoms at a site
that have a characteristic
behavior in all molecules
where it occurs
 The group reacts in a typical

way, generally independent
of the rest of the molecule
 For example, the double

bonds in simple and
complex alkenes react with
bromine in the same way
3
Functional Groups with Multiple
Carbon–Carbon Bonds
 Alkenes have a C-C
double bond
 Alkynes have a C-C
triple bond
 Arenes have special
bonds that are
represented as
alternating single
and double C-C
bonds in a six-
membered ring
4
Functional Groups with Carbon Singly
Bonded to an Electronegative Atom
5
Groups with a Carbon–Oxygen Double Bond
(Carbonyl Groups)
6
Survey of Functional Groups
7
Survey of Functional Groups
8
3.2 Alkanes and Alkane Isomers
 Alkanes: Compounds with C-C single bonds and C-H
bonds only (no functional groups)
 Connecting carbons can lead to large or small molecules
 The formula for an alkane with no rings in it must be
CnH2n+2 where the number of C’s is n
 Alkanes are saturated with hydrogen (no more can be
added
 They are also called aliphatic compounds
9
Alkane Isomers
 CH4 = methane, C2H6 = ethane, C3H8= propane
 The molecular formula of an alkane with more than
three carbons can give more than one structure
 C4 (butane) = butane and isobutane
 C5 (pentane) = pentane, 2-methylbutane, and 2,2-
dimethylpropane
 Alkanes with C’s connected to no more than 2 other
C’s are straight-chain or normal alkanes
 Alkanes with one or more C’s connected to 3 or 4 C’s
are branched-chain alkanes
10
Constitutional Isomers
 Isomers that differ in how their atoms are arranged in chains are
called constitutional isomers
 Compounds other than alkanes can be constitutional isomers
of one another
 They must have the same molecular formula to be isomers
11
Condensed Structures of Alkanes
 We can represent an alkane in a brief form or in
many types of extended form
 A condensed structure does not show bonds but lists
atoms, such as
 CH3CH2CH2CH3 (butane)
 CH3(CH2)2CH3 (butane)
12
13
3.3 Alkyl Groups
 Alkyl group – remove
one H from an alkane (a
part of a structure)
 General abbreviation “R”
(for Radical, an
incomplete species or the
“rest” of the molecule)
 Name: replace -ane
ending of alkane with -yl
ending
 CH3 is “methyl” (from
methane)
 CH2CH3 is “ethyl”
from ethane
14
15
Types of Alkyl groups
 Classified by the connection site (See Figure 3.3)
 a carbon at the end of a chain (primary alkyl group)
 a carbon in the middle of a chain (secondary alkyl
group)
 a carbon with three carbons attached to it (tertiary alkyl
group)
16
17
3.4 Naming Alkanes
 Compounds are given systematic names by a process that uses
 Follows specific rules

 Find parent hydrocarbon chain
 Carbons in that main chain are numbered in sequence
 Substituents are identified numbered
 Write compound name is single word
 Name a complex substituents as though it were a compound
itself
 See specific examples in text
 Try ThomsonNow Organic Interactive from p. 90 of
your text
18
3.5 Properties of Alkanes
 Called paraffins (low affinity compounds)
because they do not react as most chemicals
 They will burn in a flame, producing carbon
dioxide, water, and heat
 They react with Cl2 in the presence of light to
replace H’s with Cl’s (not controlled)
19
Physical Properties
 Boiling points and melting points increase as size of alkane
increases
 Dispersion forces increase as molecule size increases, resulting in
higher melting and boiling points
20
3.6 Conformations of Ethane
 Stereochemistry concerned with the 3-D
aspects of molecules
  bonds are cylindrically symmetrical
 Rotation is possible around C-C bonds in
open-chain molecules
21
Conformers
 Conformation- Different arrangement of
atoms resulting from bond rotation
 Conformations can be represented in 2 ways:
22
Torsional Strain
 We do not observe perfectly free rotation
 There is a barrier to rotation, and some
conformers are more stable than others
 Staggered- most stable: all 6 C-H bonds are
as far away as possible
 Eclipsed- least stable: all 6 C-H bonds are as
close as possible to each other
23
24
3.7 Conformations of Other
Alkanes
 The eclipsed conformer of propane has 3
interactions: two ethane-type H-H interactions, and
one H-CH3 interaction
25
Conformations of Other Alkanes
• Conformational situation is more complex for larger alkanes

• Not all staggered conformations has same energy, and not all
eclipsed conformations have same energy
26
Conformations of Butane
 Anti conformation- methyl groups are 180˚ apart
 Gauche conformation- methyl groups are 60˚ apart
Which is the most energetically stable?
27
Steric Strain
 Steric strain- repulsive interaction occurring between atoms
that are forced closer together than their atomic radii allow
28
29

Organic Compounds: Alkanes and Their Stereochemistry: Based On Mcmurry'S Organic Chemistry, 7 Edition

Uploaded by

Copyright:

Available Formats

Organic Compounds: Alkanes and Their Stereochemistry: Based On Mcmurry'S Organic Chemistry, 7 Edition

Uploaded by

Document Information

Original Title

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Organic Compounds: Alkanes and Their Stereochemistry: Based On Mcmurry'S Organic Chemistry, 7 Edition

Uploaded by

Copyright:

Available Formats

3.

Based on McMurry’s Organic Chemistry, 7th edition

 Alkanes will be used to discuss basic approaches to naming

 We will take an initial look at 3-D aspects of molecules

 The group reacts in a typical

 For example, the double

 Follows specific rules

• Conformational situation is more complex for larger alkanes

Which is the most energetically stable?

You might also like