Organic 3: Alkanes/Cycloalkanes - Conformations & cis-trans Stereoisomers Flashcards

1
Q

Conformations

A

different spatial arrangements of a molecule that are generated by rotation about single bonds

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2
Q

Conformational analysis

A

study of how conformational factors affect the structure of a molecule and its properties

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3
Q

Staggered conformation

A

each C-H bond of one carbon bisects an H-C-H angle of the other carbon

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4
Q

Eclipsed conformation

A

each C-H bond of one carbon is aligned with a C-H bond of the other carbon

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5
Q

Gauche

A

spatial relationship term used when the torsion angle is 60 degrees

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6
Q

Anti

A

spatial relationship term used when the torsion angle is 180 degrees

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7
Q

Torsional strain

A

conformations in which the torsion angles between adjacent bonds are other than 60 degrees

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8
Q

Steric strain

A

torsional and other sources of strain in molecules

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9
Q

Activation energy

A

the minimum energy that a reacting system must possess above its most stable state in order to undergo a chemical or structural change

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10
Q

Transition state

A

the point of maximum potential energy encountered in reactants as they proceed to products

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11
Q

van der Waals strain (steric hindrance)

A

destabilization of a molecule that results when 2 of its atoms are too close to each other; contributes to the total steric strain

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12
Q

Strain energy

A

deviations from the ideal values for bond angles/distances, etc will destabilize a particular structure and increase its potential energy

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13
Q

Angle strain

A

strain a molecule has because one or more of its bond angles deviate from the ideal value

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14
Q

Envelope

A

Nonplanar conformation of cyclopentane in which 4 of the carbon atoms are coplanar; the 5th carbon is out of the plane of the other 4

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15
Q

Half-chair

A

Nonplanar conformation of cyclopentane in which there are 3 coplanar carbons, with 1 carbon atom displaced above that plane and another below it

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16
Q

Chair conformation

A

most stable conformation of cyclohexane; with C-C-C bond angles of 111 degrees, it is nearly free of angle strain; all of its bonds are staggered, making it free of torsional strain as well

17
Q

Boat

A

much less stable nonplanar conformation of cyclohexane; bond angles are approximately tetrahedral; relatively free of angle strain; destabilized by torsional strain associated with eclipsed bonds on 4 of its carbons; two “flagpole” hydrogens contribute a small amount of van der Waals strain as well

18
Q

Twist boat (skew boat)

A

more stable nonplanar conformation of cyclohexane; reduces both torsional strain and van der Waals strain by a rotation about the carbon-carbon bond

19
Q

Axial hydrogens

A

6 of cyclohexane’s hydrogens have their bonds parallel to a vertical axis that passes through the ring’s center; alternately directed up or down on adjacent carbons

20
Q

Equatorial hydrogens

A

6 of cyclohexane’s hydrogens are located approximately along the equator of the molecule; 4 bonds to each carbon are arranged tetrahedrally

21
Q

Ring inversion (chair-chair interconversion)

A

one chair conformation is converted to another chair

22
Q

Intermediate

A

not a potential energy maximum, but a local minimum on the potential energy profile

23
Q

1,3-diaxial repulsions

A

repulsive forces between axial substituents on the same side of a cyclohexane ring

24
Q

Standard free energy

A

one of the fundamental equations of thermodynamics concerns systems at equilibrium and relates the equilibrium constant K to the difference in this between the products and the reactants

25
Q

cis

A

when substituents are on the same side they are ___ to each other

26
Q

trans

A

when substituents are on opposite sides they are ___ to each other

27
Q

Stereoisomers

A

isomers that have their atoms bonded in the same order (same constitution) but they differ in the arrangement of atoms in space; those of the cis-trans type are sometimes referred to as geometric isomers

28
Q

Polycyclic

A

compounds that contain more than 1 ring

29
Q

Spiro

A

a compound with one atom common to 2 rings

30
Q

Bridged

A

compound with 2 atoms common to 2 or more rings

31
Q

Heterocyclic compound

A

a substance with a ring that contains at least one heteroatom