Chapter 4 Flashcards
Hydrocarbons that lack pi bonds
saturated hydrocarbons or alkanes
nomenclature
the system of rules for naming compounds
What are the four steps of naming a compound?
- identify the parent chain
- name the substituents
- number the carbon atoms of the parent and assign a locant to each substituent
- assemble the substituents alphabetically, placing locants in front of each substituent. (for identical subst. use di, tri, tetra, penta, or hexa which are ignored when alphebetizing)
Cycloalkanes
alkanes containing a ring
Locant
number used to identify the location of a substituent
Bicycloalkane
an alkane that has two rings that are connected to one another
Differences when naming bicyclic compounds
- the term “bicyclo” is used, and bracketed numbers indicate how the bridgeheads are connected
- to number the parent, travel first along the longest path connected the bridgeheads
Heat of Combustion
(in alkanes) the negative of the change in enthalpy (-△Hº) associated with the complete combustion of 1 mol of alkane in the presence of oxygen
Can be measured experimetnally and used to compare the stability of isomeric alkanes
Cracking
a process by which C-C bonds of larger alkanes are broken, producing smalleralkanes suitable for gasoline.
Reforming
a process in which straight chain alkanes are converted into branched hydrocarbons and aromatic compounds, which exhibit less knocking during combustion
Rotation about C-C single bonds allows a compound to adopt a varitey of:
Conformations
Newman projections
a drawing style that is designed to show the conformation of a molecule
Dihedral angle
describes the relative postitions of one group on the back carbon and one group on the front carbon in a Newman projection
AKA torsional angle
torsional strain
difference in energy between staggered and eclipsed conformations of ethane
When does angle strain occur?
in cycloalkanes when bond angles are less than the preferred 109.5º