JoVE Logo
АВТОРЫ
СВЯЖИТЕСЬ С НАМИ

Войдите в систему

Core - Organic Chemistry

    Chapter 4

    Stereoisomerism

    4.1 : Chirality02:25

    4.1 : 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. ...

    23.1K views
    4.2 : Isomerism02:43

    4.2 : Isomerism

    Isomers are molecules with the same molecular formula but different structural arrangements. Isomers can be further classified into constitutional isomers ...

    17.9K views
    4.3 : Stereoisomers02:32

    4.3 : Stereoisomers

    On the basis of mirror symmetry, stereoisomers of an organic molecule can be further classified into diastereomers and enantiomers. Diastereomers are ...

    12.4K views
    4.4 : Naming Enantiomers02:21

    4.4 : Naming Enantiomers

    The naming of enantiomers employs the Cahn–Ingold–Prelog rules that involve assigning priorities to different substituent groups at a chiral ...

    19.8K views
    4.5 : Properties of Enantiomers and Optical Activity02:24

    4.5 : 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 ...

    16.7K views
    4.6 : Molecules with Multiple Chiral Centers02:25

    4.6 : 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 ...

    11.2K views
    4.7 : Fischer Projections02:18

    4.7 : Fischer Projections

    Learning to draw Fischer projections of molecules and understanding their relevance plays a crucial role in the visual depiction of organic molecules. A ...

    13.0K views
    4.8 : Racemic Mixtures and the Resolution of Enantiomers02:30

    4.8 : Racemic Mixtures and the Resolution of Enantiomers

    A racemic mixture, or racemate, is an equimolar mixture of enantiomers of a molecule that can be separated using their unique interaction with chiral ...

    18.1K views
    4.9 : Stereoisomerism of Cyclic Compounds02:33

    4.9 : Stereoisomerism of Cyclic Compounds

    In this lesson, we delve into the role of ring conformation and its stability, which determines the spatial arrangement and, consequently, the molecular ...

    8.7K views
    4.10 : Chirality at Nitrogen, Phosphorus, and Sulfur02:30

    4.10 : Chirality at Nitrogen, Phosphorus, and Sulfur

    Chirality is most prevalent in carbon-based tetrahedral compounds, but this important facet of molecular symmetry extends to sp3-hybridized nitrogen, ...

    5.7K views
    4.11 : Prochirality02:05

    4.11 : Prochirality

    The concept of prochirality leads to the nomenclature of the individual faces of a molecule and plays a crucial role in the enantioselective reaction. It ...

    3.8K views
    4.12 : Chirality in Nature02:30

    4.12 : 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 ...

    12.8K views
    JoVE Logo

    Конфиденциальность

    Условия эксплуатации

    Политика

    СВЯЖИТЕСЬ С НАМИ

    РЕКОМЕНДОВАТЬ БИБЛИОТЕКЕ

    НОВОСТИ JoVE

    Исследования

    Образование

    АВТОРЫ

    Библиотекарь

    О JoVE

    Авторские права © 2025 MyJoVE Corporation. Все права защищены