Biomolecular Bonding: Flashcards

1
Q

What are the main types of isomerism?

A
  • Structural Isomer

- Stereoisomer

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2
Q

What are the type of stereoisomers?

A
  • E/Z isomerism

- Optical isomerism

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3
Q

What are the types of structural isomers?

A
  • Chain isomer
  • Functional group isomer
  • Position isomer
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4
Q

Why is the way that atoms are joined together important?

A

Arranging it in any other way could affect whether it is still the same molecule

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5
Q

What could give rise to a number of structural isomers?

A

Particular atoms being rearranged in different molecular arrangements

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6
Q

Why are structural isomers likely to have different chemical properties?

A

The functional groups contained may be in a different order and so will exhibit different interactions and reactivity

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7
Q

What is similar and what is different between structural isomers?

A
  • Same composition/molecular formula

- Different order in which atoms are bonded together

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8
Q

What are stereoisomers?

A

Molecules with the same composition/molecular formula and order of bonding of particular atoms but different three-dimensional arrangement in space

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9
Q

What are optical isomers?

A

Compounds with the same molecular formula and order of bonding between particular atoms, but non-superimposable mirror images of each other (an enantiomers pair)

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10
Q

How are some analytical techniques used to find out what proportion of different enantiomers are present?

A

Using the fact that optical isomers have equal and opposite optical activity

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11
Q

What does it mean that a substance in enantiopure?

A

Contains only one enantiomer

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12
Q

What is a race mate?

A

A substance containing an equal proportion of each enantiomer

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13
Q

What is the optical activity of enantiomers?

A

The direction that enantiomers rotate plane-polarised light

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14
Q

When is it useful and mot useful to label molecules using the empirically derived (much older) system?

A

Useful when interested in practically differentiating enantiomers, but not useful for defining stereochemical arrangements for molecules where we don’t know their properties

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15
Q

List the symbols that the empirically derived system uses:

A

(+)- or (-)-

d- or l- (both lower case)

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16
Q

What does it mean that enantiomers of a compound will have an equal and opposite optical activity?

A

Each enantiomer will rotate Plane polarised light by the same degree but in different directions

17
Q

Why is stereochemistry important when understanding molecules?

A

Molecules behave in specific ways depending on their stereochemistry

18
Q

What is a stereocentre?

A

A geometric point in space