Test 2 Materials Flashcards

End of Chapter 3, Chapter 4 and Chapter 5

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.

A

Anti

17
Q

general formula of a cycloalkane

A

CnH2n

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.

A

angle strain

20
Q

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

A

equatorial

21
Q

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

A

handedness

22
Q

non-superimposable mirror images which come in pairs

A

Enantiomers

23
Q

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

A

achiral

24
Q

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

A

chiral

25
Q

if a molecule has a plane of symmetry it is

A

achiral

26
Q

an enantiomer which rotates light counter clockwise is labeled negative and is called

A

levorotatory

27
Q

an enantiomer which rotates light clockwise is labeled positive and is called

A

dextrorotatory

28
Q

the extent to which an enantiomer rotates light is dependent on

A

the # of optically active molecules in the sample

29
Q

when ranking atoms to determine configuration, atoms are ranked by their __

A

atomic number

30
Q

R configuration

A

a clockwise path from atom 1 to 3 around the chiral center

31
Q

s configuration

A

a counter clockwise path from atom 1 to 3 around the chiral center

32
Q

Optical rotation sign (is/is not) related to R/S configuration.

A

IS NOT

33
Q

This stereoisomer is oppositely configured at every chiral center.

A

Enantiomers

34
Q

This stereoisomer is identical except for 1 chiral center

A

epimer

35
Q

this stereoisomer is oppositely configured at some chiral centers

A

diastereomer

36
Q

a molecule which contains chiral centers but do have a plane of symmetry. These molecules do not rotate polarized light.

A

meso compound

37
Q

a 50:50 mixture of enantiomers

A

racemic mixture, a racemate