Optical Isomers and Enantiomers Quiz
8 Questions
5 Views

Choose a study mode

Play Quiz
Study Flashcards
Spaced Repetition
Chat to lesson

Podcast

Play an AI-generated podcast conversation about this lesson

Questions and Answers

What defines a chiral centre in a molecule?

  • A carbon atom bonded to three identical groups.
  • A carbon atom that is connected to a double bond.
  • A carbon atom with four different groups bonded to it. (correct)
  • A carbon atom that has no bonds with hydrogen.

    • What are enantiomers?

  • Isomers that differ in the arrangement of atoms but not bonds.
  • Optical isomers that are mirror images of each other. (correct)
  • Isomers that rotate plane polarized light in the same direction.
  • Molecules that have the same structural formula.

    • What occurs in a racemic mixture?

  • It consists of only one enantiomer.
  • It is formed from a symmetrical carbon.
  • It rotates polarized light in one direction.
  • It has a 1:1 ratio of two different enantiomers. (correct)

    • How do nucleophilic addition reactions lead to the formation of optical isomers?

    <p>By allowing nucleophiles to attack from both sides of the carbon-oxygen double bond.</p> Signup and view all the answers

    What is the effect of enantiomers on plane polarized light?

    <p>Each enantiomer rotates polarized light in opposite directions.</p> Signup and view all the answers

    Which statement about optical isomers is correct?

    <p>They must contain at least one chiral centre.</p> Signup and view all the answers

    What is the overall effect of a racemic mixture on polarized light?

    <p>It has a neutral effect and does not rotate light.</p> Signup and view all the answers

    How can the presence of a chiral centre in a molecule be indicated?

    <p>By marking the carbon with an asterisk (*)</p> Signup and view all the answers

    Study Notes

    Optical Isomers

    • Optical isomerism is a type of stereoisomerism where molecules have the same molecular formula but a different spatial arrangement of atoms.
    • Optical isomers occur when there is an asymmetrical carbon within an organic molecule known as a chiral centre.
    • A chiral centre is a carbon atom with four different groups bonded around it so there is no line of symmetry to the molecule.

    Enantiomers

    • The presence of a chiral centre leads to the presence of two possible isomers that are mirror images of each other.
    • These are optical isomers, also known as enantiomers.
    • Enantiomers are unique because they have different effects on plane polarised light.
    • Each enantiomer rotates plane polarised light by 90 degrees in opposite directions.

    Racemic Mixtures

    • A racemate is formed when optical isomers are produced as a pair of enantiomers in a 1:1 ratio.
    • The opposite directions of rotation of the enantiomers in a racemic mixture cancel each other out, making the mixture optically inactive.
    • Racemic mixtures are formed as a result of nucleophilic addition reactions.

    Nucleophilic Addition Reactions

    • Nucleophiles can attack a molecule with a carbonyl group from above or below the carbon-oxygen double bond.
    • This produces two possible products that are mirror images, and therefore optical isomers.

    Studying That Suits You

    Use AI to generate personalized quizzes and flashcards to suit your learning preferences.

    Quiz Team

    Related Documents

    AQA Chemistry A-level 3.3.7: Optical Isomers PDF

    Description

    Test your knowledge on optical isomerism and enantiomers with this quiz. Explore the concepts of chiral centers, racemic mixtures, and their effects on plane polarized light. Perfect for students of organic chemistry.

    More Like This

    Use Quizgecko on...
    Browser
    Open
    Browser
    Browser