Chapter 3 Flashcards

(7 cards)

1
Q

Alkanes and formula

A

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)

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2
Q

Hydrocarbon names (1-10)

A
1= meth
2= eth
3= prop
4= but
5=pent
6=hex
7=hept
8=oct
9=non
10=dec
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3
Q

Nomenclature Rules

A

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

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4
Q

Alkyl Groups

A

primary (1) only 1 R attachment
secondary (2
) two R attachments
Tertiary (3*) 3 R attachments

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5
Q

Use of Alkanes

A
C1-C2 Liquefied Natural Gas
C3-C4 Liquefied Petroleum Gas
C5-C8 Gasoline
C9-C16 Kerosene and Diesel Fuel
C16+ Mineral Oils
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6
Q

Sources of alkanes

A

Fractional Distillation of Crude Oil

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7
Q

Reactions of Alkanes

A
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
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