Test 2 Materials Flashcards

End of Chapter 3, Chapter 4 and Chapter 5 (37 cards)

1
Q

isopropyl

A

a 2 carbon branch plus a methyl

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2
Q

isobutyl

A

a 3 carbon branch plus a methyl on the second carbon

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3
Q

isopentyl

A

a 4 carbon branch plus a methyl

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4
Q

sec-butyl

A

a 3 carbon branch plus a methyl on the first carbon

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5
Q

neopentyl

A

a 3 carbon branch with 2 methyl groups on the 2nd carbon

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6
Q

tert-pentyl

A

a 3 carbon branch with 2 methyl groups on the 1st carbon

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7
Q

Alkanes are relatively ___ (reactive or inert). They do react with ___, and ___ under ultraviolet light.

A

Inert; Oxygen; Halides

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8
Q

Alkanes with higher molecular weights have ___ boiling points.

A

Higher

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9
Q

Alkanes with equal molecular weights but more branching have ___ boiling points due to dispersion forces.

A

Lower

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10
Q

Different arrangements of atoms due to bond rotation are called:

A

conformations

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11
Q

A dihedral angle

A

The angle between two intersecting planes (planes created by two sets of three atoms).

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12
Q

Which conformation is more stable, staggered or eclipsed?

A

Staggered. The dihedral angles are greater.

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13
Q

Electron repulsion between eclipsed bonds.

A

torsional strain

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14
Q

Repulsion interaction when atoms are forced closer together than atomic radii allows

A

steric hindrance

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15
Q

a staggered conformation with two high energy substituents next to each other.

A

Gauche

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16
Q

a staggered conformation with two high energy substituents opposing each other.

17
Q

general formula of a cycloalkane

18
Q

These isomers have atoms connected in the same order but different 3D orientation.

A

stereoisomers

19
Q

Strain caused by bond angles forced to deviate from ideal 109 degrees.

20
Q

Larger substituents experience greater steric hindrance and are happier in the ___ position.

21
Q

the consequence of the tetrahedral stereochemistry of sp3-hybridized C atoms. Sp3 hybridized C atoms with 4 unique substituents have this quality.

22
Q

non-superimposable mirror images which come in pairs

23
Q

a molecule that is superimposable on it’s mirror image is

24
Q

a molecule that is not identical to its mirror image is said to be

25
if a molecule has a plane of symmetry it is
achiral
26
an enantiomer which rotates light counter clockwise is labeled negative and is called
levorotatory
27
an enantiomer which rotates light clockwise is labeled positive and is called
dextrorotatory
28
the extent to which an enantiomer rotates light is dependent on
the # of optically active molecules in the sample
29
when ranking atoms to determine configuration, atoms are ranked by their __
atomic number
30
R configuration
a clockwise path from atom 1 to 3 around the chiral center
31
s configuration
a counter clockwise path from atom 1 to 3 around the chiral center
32
Optical rotation sign (is/is not) related to R/S configuration.
IS NOT
33
This stereoisomer is oppositely configured at every chiral center.
Enantiomers
34
This stereoisomer is identical except for 1 chiral center
epimer
35
this stereoisomer is oppositely configured at some chiral centers
diastereomer
36
a molecule which contains chiral centers but do have a plane of symmetry. These molecules do not rotate polarized light.
meso compound
37
a 50:50 mixture of enantiomers
racemic mixture, a racemate