Related Experiment Video

Updated: Apr 26, 2026

Coulomb Explosion Imaging as a Tool to Distinguish Between Stereoisomers
08:51

Coulomb Explosion Imaging as a Tool to Distinguish Between Stereoisomers

Published on: August 18, 2017

9.6K

Eigen oscillations of a chiral sphere and their influence on radiation of chiral molecules

V V Klimov, I V Zabkov, A A Pavlov

    Optics Express
    |August 5, 2014
    PubMed

    More Related Videos

    Stimulated Stokes and Antistokes Raman Scattering in Microspherical Whispering Gallery Mode Resonators12:21

    Stimulated Stokes and Antistokes Raman Scattering in Microspherical Whispering Gallery Mode Resonators

    Published on: April 4, 2016

    10.7K
    Induction of Microstreaming by Nonspherical Bubble Oscillations in an Acoustic Levitation System08:19

    Induction of Microstreaming by Nonspherical Bubble Oscillations in an Acoustic Levitation System

    Published on: May 9, 2021

    2.5K

    Related Concept Videos

    Chirality in Nature02:30

    Chirality in Nature

    Chirality is the most intriguing yet essential facet of nature, governing life’s biochemical processes and precision. It can be observed from a snail shell pattern in a macroscopic world to an amino acid, the minutest building block of life. Most of the snails around the world have right-coiled shells because of the intrinsic chirality in their genes. All the amino acids present in the human body exist in an enantiomerically pure state, except for glycine - the sole achiral amino acid.
    13.4K
    Chirality02:25

    Chirality

    Chirality is a term that describes the lack of mirror symmetry in an object. In other words, chiral objects cannot be superposed on their mirror images. For example, our feet are chiral, as the mirror image of the left foot, the right foot, cannot be superposed on the left foot.
    Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
    23.1K
    Properties of Enantiomers and Optical Activity02:24

    Properties of Enantiomers and Optical Activity

    It is essential to understand the difference between chiral and achiral interactions and the implications thereof in optical activity and their applications. Just as our feet, which are chiral, interact uniquely with chiral objects, such as a pair of shoes, but identically with achiral socks, enantiomers of a molecule exhibit different properties only when they interact with other chiral media. An example of a significant implication from this facet is the phenomenon known as optical activity,...
    16.0K
    Molecules with Multiple Chiral Centers02:25

    Molecules with Multiple Chiral Centers

    Molecules that possess multiple chiral centers can afford a large number of stereoisomers. For instance, while some molecules like 2-butanol have one chiral center, defined as a tetrahedral carbon atom with four different substituents attached, several molecules like butane-2,3-diol have multiple chiral centers. A simple formula to predict the number of stereoisomers possible for a molecule with n chiral centers is 2n. However, there can be a lower number where some of the stereoisomers are...
    11.5K
    ¹H NMR Chemical Shift Equivalence: Enantiotopic and Diastereotopic Protons00:58

    ¹H NMR Chemical Shift Equivalence: Enantiotopic and Diastereotopic Protons

    Replacing each alpha-hydrogen in chloroethane by bromine (or a different functional group) yields a pair of enantiomers. Such protons are called prochiral or enantiotopic and are related by a mirror plane. Enantiotopic protons are chemically equivalent in an achiral environment. Because most proton NMR spectra are recorded using achiral solvents, enantiotopic hydrogens yield a single signal.
    In chiral compounds such as 2-butanol, replacing the methylene hydrogens at C3 produces a pair of...
    3.7K
    Radical Halogenation: Stereochemistry01:33

    Radical Halogenation: Stereochemistry

    Stereochemistry is the study of the different spatial arrangements of atoms in a given molecule. The stereochemistry of radical halogenations can be understood from three different situations:
    Halogenation to form a new chiral center:
    3.6K