Ch 2 Alkanes and Organic Nomenclature Flashcards

1
Q

Hydrocarbon

A

carbon and hydrogen only

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2
Q

4 Cs of chemical structure

A

Composition - elements
Constitution - connectivity
Configuration - arrangement
Conformation - arrangement with bonds on different atoms

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3
Q

Alliphatic hydrocarbons

A

Alkanes - 1x bond (C n, H 2n+2)
Alkene - 2x bond (C n, H 2n)
Alkyl - 3x bond (C n, H 2n-2)

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4
Q

Aromatic hydrocarbons

A

have benzene ring

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5
Q

n-Alkane (“normal”)

A

-unbranched alkane

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6
Q

Skeletal structure

A
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7
Q

Cycloalkanes

A

Alkanes in a circular chain
-have fewer Hs

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8
Q

Isomers

A

different compounds with the same molecular formula
-connectivity: constitutional/structural isomers

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9
Q

IUPAC

A

slides 13 - 23

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10
Q

Cycloalkane nomenclature

A

IUPAC + cyclo

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11
Q

Carbon classification

A

Primary - bonded to one other C
Secondary - two other Cs
Tertiary - three other Cs
Quaternary - four other Cs

(same name applies to their hydrogens)

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12
Q

Conformations!

A

-very fast
Rotating about a single bond (double and triple are too close to move around); leads to different dihedral angles
Ways to show:
-Newman projection
-Line and wedge
-Sawhorse projection

Eclipsed conformation: torsional strain
*usually are just transition states (not set)

Staggered conformation: more stable than eclipsed (each atom has own room for electrons)
-Gauche (60 degrees)
-Anti (180 degrees)
*favored
*most stable conformation of staggered is favored

-van der Waals repulsions happen when radii are squished too close (less stable)

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13
Q

Alkanes

A

Boiling Point
-unbranched: BP increases with each carbon

Melting Point
-used to identify compounds
-narrow melting point: purer
-increases with carbon number
-lowers with branching (more SA)
-symmetry: very high MP

Dipole Moment
-negligible dipole moments
-nonpolar

Solubility
-insoluble in water

Density
-less dense than water (many oils are Alkanes)

Combustion
-least reactive of organic compounds
-react quickly with O2 to make CO2 and H2O

*make many functional groups

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14
Q

Functional Groups

A

characteristically bonded group of atoms

‘R’ - a generic functional group
‘Ph-‘ - phenyl group
‘Ar’ - commonly substituted ring (Aromatic)

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15
Q

Compound Classes

A

compounds with same functional group

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