An introduction to A level organic chemistry Flashcards

1
Q

Explain what is meant by delocalized electrons in benzene.

A

Electrons that are free to move around the molecule in the pi bonding system above and below the plane of carbon atoms in benzene ring.

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2
Q

Define racemic mixture.

A

A mixture containing equal amount of a pair of enantiomers.

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3
Q

Explain the meaning of optically active.

A

A substance that is able to rotate the plane of polarised light.

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4
Q

Give two reasons why it might be desirable to synthesise a single optical isomer for use as a drug.

A
  1. Other isomer can have side effects.
  2. Avoid the need to separate the optical isomer to form the pure active isomer.
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5
Q

How to produce a single / pure enantiomer?

A

Chiral catalyst.

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6
Q

How to separate two enantiomers?

A

Optical resolution using chiral auxiliary.

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7
Q

Define chiral auxiliary.

A

A special molecule that only interact with one type of isomer in a mix.

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8
Q

Define enantiomers.

A

Molecules that rotate the plane of polarised light in opposite directions.

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9
Q

Suggest one disadvantage of producing two enantiomers in a synthesis.

A

Lower yield of biologically active molecule.

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