Optical Isomerism (OCR A Level Chemistry A): Flashcards

Exam code: H432

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  • Define stereoisomers

Cards in this collection (14)

  • Define stereoisomers

    Stereoisomers are molecules that have the same structural formula but have their atoms arranged differently in space.

  • Define chiral centre

    A chiral centre is a carbon atom bonded to four different atoms or groups of atoms, giving rise to optical isomers.

  • What structural feature makes a carbon atom a chiral centre?

    A carbon atom bonded to four different atoms or groups of atoms is a chiral centre.

  • How can you confirm a carbon atom is NOT a chiral centre?

    If the carbon is bonded to two identical atoms or groups of atoms, it cannot be a chiral centre.

  • Define enantiomers

    Enantiomers are the two optical isomers of a chiral molecule, which are non-superimposable mirror images of each other.

  • Chiral centres are commonly marked with an .......... in structural drawings.

    Chiral centres are commonly marked with an asterisk in structural drawings.

  • A carbon atom bonded to .......... different atoms or groups of atoms is called a .......... carbon.

    A carbon atom bonded to four different atoms or groups of atoms is called a chiral carbon.

  • When identifying chiral centres from a molecular formula, what should you do first?

    Draw the molecule as a condensed structural formula or displayed formula so all bonds and groups are visible.

  • Why does a molecule with a chiral centre exist as two distinct optical isomers?

    The four different groups on the chiral carbon can be arranged in two non-superimposable ways, producing two enantiomers that are mirror images of each other.

  • True or False?

    A carbon atom bonded to two identical groups can be a chiral centre.

    False.

    A chiral centre requires four different groups; two identical groups mean the carbon cannot be a chiral centre.

  • True or False?

    Enantiomers are superimposable mirror images of each other.

    False.

    Enantiomers are non-superimposable mirror images, meaning one cannot be placed on top of the other to give an identical arrangement.

  • In a 3D stereochemical drawing, what does a solid wedge bond represent?

    A solid wedge represents a bond coming out of the plane of the paper towards the viewer.

  • What two types of stereoisomerism exist in organic chemistry?

    1. Geometrical (E/Z) stereoisomerism

    2. Optical stereoisomerism

  • True or False?

    A dotted line in a stereochemical drawing represents a bond receding behind the plane of the paper.

    True.

    A dotted line (or hatched wedge) shows a bond going behind the plane of the paper, away from the viewer.

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