Chapter 3 Flashcards
(7 cards)
Alkanes and formula
fully saturated hydrocarbons.
Solubilities= good in nonpolar solvents and hyrdophobic
Denisty= less dense than water(1.0) at .7
Boiling and Melting Point= increases with size and molecular mass
Formula –> Cn H(2n+2)
Hydrocarbon names (1-10)
1= meth 2= eth 3= prop 4= but 5=pent 6=hex 7=hept 8=oct 9=non 10=dec
Nomenclature Rules
1) Find the longest chain of C atoms and name it
2) Number the longest chain beginning with the nearest constituent and least amount of branches
3) Name the substituent groups attached to the longest chain as alkyl groups. Give location of each alkyl groups by the number of the main-chain C atom to which it is attached
4) When two or more substituents are present, list them in alphabetical order. When two or more of the same alkyl groups are present use prefixes to avoid naming the same group twice
Alkyl Groups
primary (1) only 1 R attachment
secondary (2) two R attachments
Tertiary (3*) 3 R attachments
Use of Alkanes
C1-C2 Liquefied Natural Gas C3-C4 Liquefied Petroleum Gas C5-C8 Gasoline C9-C16 Kerosene and Diesel Fuel C16+ Mineral Oils
Sources of alkanes
Fractional Distillation of Crude Oil
Reactions of Alkanes
Combustion- O2 always present, CO2 and H20 ALWAYS FORMED Catalytic Hydrocracking (Heat and H2 as a catalyst)- Forms shorter-chain alkanes (hydrated) Catalytic Cracking (Heat catalyst) - form shorter-chain alkanes and alkenes Halogenation (heat or light)- add halogen which breaks up hydrocarbon into random derivatives