Organic Chemistry Chapter 2: Isomers Flashcards

1
Q

What are structural isomers?

A

Share only a molecular formula. They have different physical and chemical properties.

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2
Q

What are conformational isomers?

A

They differ by rotation around a single sigma bond.

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3
Q

What are staggered conformations? anti staggered? gauche staggered?

A

have groups 60 degrees apart.
In anti-staggered, the two largest groups are 180 degrees apart, and strain is minimized.
In gauche, the two largest are 60 degrees apart.

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4
Q

What is an eclipsed conformation?

A

Have groups directly in front of each other. In totally eclipsed conformations, the two largest groups are directly in front of each other and the strain is maximized.

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5
Q

What are the three types of strain?

A

angle strain, torsional strain and non bonded strain

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6
Q

What is angle strain?

A

It is the stretching or compressing angles from their normal size, happens in cyclic molecules

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7
Q

What is torsional strain?

A

It is from eclipsing conformations

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8
Q

What is non bonded strain?

A

Happens because of interactions between substituents attached to nonadjacent carbons.

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9
Q

Which creates more non bonded strain - axial or equatorial?

A

axial

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10
Q

What are configurational isomers?

A

can only be interchanged by breaking and reforming bonds.

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11
Q

What are enantiomers?

A

Nonsuperimposable mirror images and thus have opposite stereochemistry at every chiral carbon. They have the same chemical and physical properties except for rotation of plane-polarized light and reactions in a chiral environment.

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12
Q

What is optical activity?

A

Refers to the ability of a molecule to rotate plane-polarized light d- or (+) molecules rotate light to the right; L- or (-) molecules rotate light to the left.

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13
Q

When are there chiral carbons, but no optical activity?

A

In racemic mixtures, when there are equal concentrations of two enantiomers, their rotations cancel each other out and there will be no optical activity.

Also Meso compounds - they have an internal plane of symmetry, so the two sides cancel each other out.

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14
Q

What are diastereomers?

A

non-mirror-image stereoisomers. They differ at some, but not all chiral center. They have different chemical and physical properties.

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15
Q

What are cis-trans isomers?

A

subtype of diastereomers in which groups differ in position about an immovable bond, such as a double bond or in a cycloalkane.

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16
Q

What is a chiral center?

A

A chiral center has four different groups attached to the central carbon.

17
Q

What is relative configuration?

A

Gives the stereochemistry of a compound in comparison to another molecule.

18
Q

What is absolute configuration?

A

Gives the stereochemistry of a compound in comparison to other molecules.

19
Q

What are the Cahn-Ingold-Prelog priority rules?

A

Priority is given looking at atoms connected to the chiral carbon or double bonded carbons; whichever has the highest atomic number gets highest priority. If there is a tie, move out from the chiral or double bonded carbon until broken.

20
Q

How do you determine if an alkene is Z or E?

A
Z = highest priority substituents are on the same side of the double bond. 
E = highest priority substituents are on opposite sides of the double bond.
21
Q

How do you determine if a chiral atom is in S or R configuration?

A

Lowest priority group goes in the back and a circle is drawn from group 1 to 3. If clockwise, it is R. If counterclockwise, then it is S.

22
Q

Rotating a Fischer projection 90 degrees or switching one pair of substituents…

A

inverts the stereochemistry

23
Q

Rotating Fischer projection 180 degrees or switching two pairs of substituents… retains the stereochemistry.

A

maintains the stereochemistry