ochem chapter 2 Flashcards

1
Q

iosmers

A

are chemical compounds that have the same molecular formula but differ in structure- that is, in their atomic connectivity, or the spatial orientation of their atoms

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2
Q

structural isomers

A

are compounds that share only their molecular formula. Because their connectivities may be completely different, they often have different chemical and physical properties (such as melting point, boiling point, solubility, etc)

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3
Q

stereoisomers

A

are compounds that differ from each other only in the way that their atoms are oriented in space.

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4
Q

geometric isomers

A

are compounds that differ in the position of substituents attached to a double bond

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5
Q

cis

A

if two substituents are on the same side of the double bond

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6
Q

trans

A

if they are on opposite sides of the double bond

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7
Q

Z

A

if the two highest priority substituents on each carbon lie on the same side of the double bond

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8
Q

E

A

if they are on opposite sides

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9
Q

chiral

A

an object that is not superimposible upon its mirror image

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10
Q

achiral

A

are mirror images that can be superimposed

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11
Q

enantiomers

A

chiral objects that are non-superimposable mirror imaages

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12
Q

configuration

A

is the spatial arrangement of the atoms or groups of a stereoisomer

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13
Q

relative configuration

A

of a chiral molecule is its configuration in relation to another chrial molecule

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14
Q

absolute configuration

A

of a chiral molecule describes the spatial arrangement of these atoms or groups

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15
Q

racemic mixture

A

is a mixture of equal concentrations of both the (+) or (-) enantiomers. The rotations cancel each other and no optical activity is observed

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16
Q

polarizer

A

allows light waves oscillating only in a particular direction to pass, producing plane-polarized light

17
Q

conformational isomers

A

are compounds that differ only by rotation about one or more single bonds