Lecture 7: Structural Features of Alkanes Flashcards

1
Q

Compounds with the same molecular formula but different connections between atoms.

A

Consitutional Isomers.

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2
Q

Compounds with the same molecular formula and connections but arranged differently in space.

A

Stereoisomers

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3
Q

Molecules in which the 3D arrangement of atoms results from rotation around a single sigma bond.

A

Conformational Isomers

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4
Q

Conformation in which all atoms align with each other.

A

Eclipsed

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5
Q

Conformation in which all atoms are out of line with each other.

A

Staggered

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6
Q

Angle between the C-H bonds on the front carbon and the C-H bonds on the back carbon.

A

Dihedral Angle

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7
Q

Conformation which has the highest energy.

A

Total Eclipsed Conformation.

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8
Q

Conformation which has the lowest energy.

A

Anti conformation.

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9
Q

Dihedral Angle of eclipsed conformation.

A

0

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10
Q

Dihedral Angle of staggered conformation

A

60

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11
Q

Low/intermediate energy conformation in which the CH3 groups are close but not aligned

A

Gauche

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12
Q

Instability caused by adjacent C-H bonds eclipsing each other.

A

Torsional Strain

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13
Q

A strain-free, non-planar conformation with bond angles of 111 degrees.

A

Chair conformation.

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14
Q

H atoms lying in the same plane as the C atoms in chair conformation.

A

Equatorial

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15
Q

H atoms lying above and below the plane.

A

Axial

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16
Q

Atom interactions present in chair conformation which are highly unfavorable due to steric interactions.

A

1,3-diaxial interactions.

17
Q

Isomer which both methyl groups are on the same side of the ring.

A

Cis Isomer

18
Q

Isomer which both methyl groups are on opposite sides of the ring.

A

Trans Isomer

19
Q

Placing the _____ group in an equatorial position is preferred to reduce steric interference and 1,3-diaxial interactions.

A

Largest