Isomerism in Organic Chemistry
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Questions and Answers

What type of isomers have different positions of a functional group on the carbon chain?

  • Positional isomers (correct)
  • Functional group isomers
  • Chain isomers
  • Structural isomers
  • Stereoisomers have the same molecular formula and different sequences of atoms.

    False (B)

    What are the two main types of stereoisomers?

    Cis-trans isomers and optical isomers

    Keto-enol tautomerism involves the movement of a ______ and a double bond.

    <p>hydrogen atom</p> Signup and view all the answers

    Match the following isomers with their descriptions:

    <p>Chain isomers = Differ in branching of the carbon chain Cis-trans isomers = Result from restricted rotation due to double bonds Optical isomers = Non-superimposable mirror images Functional group isomers = Differ in the type of functional group present</p> Signup and view all the answers

    What is a racemic mixture?

    <p>A mixture with equimolar amounts of two enantiomers. (D)</p> Signup and view all the answers

    The optical inactivity of meso-tartaric acid is due to external compensation.

    <p>False (B)</p> Signup and view all the answers

    Which of the following statements about chiral molecules is true?

    <p>Chiral molecules are asymmetric and do not have superimposable mirror images. (C)</p> Signup and view all the answers

    What does external compensation explain about racemic mixtures?

    <p>The optical inactivity due to equal rotation in opposite directions by the enantiomers.</p> Signup and view all the answers

    Achiral molecules have a plane of symmetry and their mirror images are non-superimposable.

    <p>False (B)</p> Signup and view all the answers

    What does the symbol '(-)' signify in the context of isomer nomenclature?

    <p>It indicates that the isomer rotates the plane of polarization of light in an anticlockwise direction.</p> Signup and view all the answers

    The term used for a mixture containing two optical isomers in equal amounts is called a __________ mixture.

    <p>racemic</p> Signup and view all the answers

    Match the isomer types to their descriptions:

    <p>Racemic mixture = Optically inactive due to external compensation Meso-tartaric acid = Achiral with a symmetric plane Chiral carbon = Carbon atom bonded to four different groups Optical isomer = Compounds that are non-superimposable mirror images</p> Signup and view all the answers

    A carbon atom that is attached to four different types of atoms or groups of atoms is called a ______.

    <p>chiral carbon</p> Signup and view all the answers

    Match the following terms with their definitions:

    <p>Chiral molecule = Does not possess a plane of symmetry Achiral molecule = Possesses a plane of symmetry Enantiomers = Non-superimposable mirror images Meso compound = Identical compounds with a plane of symmetry</p> Signup and view all the answers

    Flashcards

    Isomers

    Different compounds with the same molecular formula but different structural arrangements.

    Structural Isomers

    Isomers with the same molecular formula but different arrangements of the atoms within the molecule.

    Positional Isomers

    Isomers with the same functional group but at different positions along the carbon chain.

    Stereoisomers

    Isomers with the same molecular formula but different spatial arrangements of the atoms, without breaking or changing any bonds.

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    Optical Isomers (Enantiomers)

    Stereoisomers that are mirror images of each other and cannot be superimposed.

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    Chiral Carbon

    A carbon atom bonded to four different atoms or groups.

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    Chiral Molecule

    A molecule without a plane of symmetry and a non-superimposable mirror image.

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    Achiral Molecule

    A molecule with a plane of symmetry and a superimposable mirror image.

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    Dextrorotatory Isomer (+)

    An isomer that rotates the plane of polarized light in a clockwise direction.

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    Levorotatory Isomer (-)

    An isomer that rotates the plane of polarized light in an anticlockwise direction.

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    Racemic Mixture

    A mixture containing equal amounts of two enantiomers, resulting in no net optical rotation.

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    Internal Compensation

    The cancellation of optical activity in a molecule due to the presence of two chiral centers with opposite configurations.

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    External Compensation

    Optical inactivity of a racemic mixture caused by the equal and opposite rotations of its enantiomers.

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    Meso Isomer

    An isomer that is optically inactive due to internal compensation, possessing a plane of symmetry that divides the molecule into two identical halves.

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    Resolution of a Racemic Mixture

    The process of separating a racemic mixture into its individual enantiomers.

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