Organic 7: Stereochemistry Flashcards

1
Q

Stereoisomers

A

isomers that have the same constitution but differ in the spatial arrangement of their atoms

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2
Q

Chiral

A

object not superimposable on its mirror image; a molecule is this if its 2 mirror-image forms are not superimposable in 3 dimensions

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3
Q

Achiral

A

a molecule that is superimposable on its mirror image

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4
Q

Enantiomers

A

stereoisomers that are related as an object and its nonsuperimposable mirror image; describes a particular relationship between 2 objects; a chiral molecule can have only one of these

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5
Q

Chirality center

A

an atom that has 4 nonequivalent atoms or groups attached to it; at various times, these have been called asymmetric centers or stereogenic centers

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6
Q

Plane of symmetry

A

bisects a molecule so that one half of the molecules is the mirror image of the other half

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7
Q

Center of symmetry

A

a point in the center of a molecule is this if any line drawn from it to some element of the structure will, when extended an equal distance in the opposite direction, encounter an identical element

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8
Q

Optical activity

A

ability of a chiral substance to rotate the plane of plane-polarized light

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9
Q

Polarimeter

A

instrument that measures optical activity

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10
Q

Racemic mixtures

A

mixtures containing equal quantities of enantiomers; optically inactive

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11
Q

Optically pure

A

at the limit, where all the molecules are of the same handedness

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12
Q

Enantiomeric excess

A

optical purity; percent of major enantiomer - percent of minor enantiomer

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13
Q

Specific rotation

A

effects of path length and concentration symbolized by alpha; a physical property; optical purity can be calculated [(___ of sample/___ of pure enantiomer) x 100]

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14
Q

Absolute configuration

A

the exact 3D spatial arrangement of substituents at a chirality center

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15
Q

Relative configurations

A

stereochemical configuration on a comparative, rather than an absolute, basis; terms such as D, L, erythro, threo, alpha, and beta describe relative configuration

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16
Q

Cahn-Ingold-Prelog System

A

AKA the sequence rules; system that deals with the problem of the absolute configuration at a chirality center

17
Q

Fischer Projections

A

always generated the same way - the molecule is oriented so that the vertical bonds at the chirality center are directed away from you and the horizontal bonds point toward you; a projection onto the page is a cross; the chirality center lies at the center of the cross but is not explicitly shown

18
Q

Prochiral

A

addition to either face converts an achiral reactant to a chiral product

19
Q

Enantiotopic

A

product from reaction at 1 face is the enantiomer of the product from reaction at the other

20
Q

Prochirality center

A

an atom of a molecule that becomes a chirality center when 1 of its attached atoms or groups is replaced by a different atom or group

21
Q

Diastereomers

A

stereoisomers that are not mirror images; cis & trans isomers of a particular compound are ___ of each other

22
Q

Erythro

A

when the carbon chain is vertical and like substituents are on the same side of the Fischer projection, the molecule is described as this type of diastereomer

23
Q

Threo

A

when like substituents are on opposite sides of the Fischer projection, the molecules is described as this type of diastereomer

24
Q

Meso forms

A

achiral molecules that have chirality centers

25
Q

Conformational enantiomers

A

enantiomers interconvertible by a conformational change

26
Q

Stereospecific reaction

A

reaction in which stereoisomeric starting materials yield products that are stereoisomers of each other

27
Q

Diastereotopic

A

describing 2 atoms or groups in a molecule that are attached to the same atom but are in stereochemically different environments that are not mirror images of each other

28
Q

Resolution

A

the separation of a racemic mixture into its enantiomeric components

29
Q

Kinetic resolution

A

separation of enantiomers based on their unequal rates of reaction with a chiral reactant

30
Q

Enzymatic resolution

A

resolution of a mixture of enantiomers based on the selective reaction of one of them under conditions of enzyme catalysis