All
Research
Education
Badania
Edukacja
Business
Rozwiązania
PL
EN - English
CN - 中文
DE - Deutsch
ES - Español
KR - 한국어
IT - Italiano
FR - Français
PT - Português
TR - Türkçe
JA - 日本語
PL - Polski
RU - Русский
HE - עִברִית
AR - العربية
Zaloguj się
Chapter 3
The formation of carbon-carbon bonds leading to the creation of the carbon chain is the basis of organic chemistry. August Kekulé and Archibald Scott ...
Organic compounds of the same molecular formula can have different structural formulas called constitutional isomers, and the phenomenon is known as ...
In the late 19th-century, the number of new chemical compounds discovered increased tremendously. Hence, the necessity arose to develop a naming system ...
Alkanes are nonpolar molecules due to the presence of only carbon and hydrogen atoms. The electronegativity difference between carbon and hydrogen is ...
Different notations are used to represent the three-dimensional structure of molecules on two-dimensional surfaces. One of the most commonly used ...
In an organic molecule, free rotation about the carbon-carbon single bond results in energetically different conformers of the molecule. Due to this ...
Unlike ethane and propane that have only two major conformations, butane has more than two conformers. The staggered form of butane in which the bulky ...
Cycloalkanes are saturated cyclic hydrocarbons with carbon atoms arranged in the form of rings. They have two fewer hydrogen atoms than the corresponding ...
Adolf von Baeyer attempted to explain the instabilities of small and large cycloalkane rings using the concept of angle strain — the strain caused ...
Cyclohexane does not exist in a planar form due to the high angle and torsional strain it would experience in the planar structure. Instead, it adopts ...
The chair conformation is the most stable form of cyclohexane due to the absence of angle and torsional strain. The absence of angle strain is a result of ...
This lesson discusses the stability of substituted cyclohexanes with a focus on energies of various conformers and the effect of 1,3-diaxial ...
Depending upon the different spatial orientation of the substituents, the disubstituted cycloalkanes exhibit two types of stereoisomers. The cis isomers ...
The low reactivity in alkanes can be attributed to the non-polar nature of C–C and C–H σ bonds. Alkanes, therefore, were initially ...
Prywatność
Warunki Korzystania
Zasady
Skontaktuj Się z Nami
Poleć Bibliotece
BIULETYNY JoVE
JoVE Journal
Methods Collections
JoVE Encyclopedia of Experiments
Archiwum
JoVE Core
JoVE Science Education
JoVE Lab Manual
JoVE Quiz
JoVE Playlist
Autorzy
Bibliotekarze
Dostęp
O JoVE
JoVE Sitemap
Copyright © 2025 MyJoVE Corporation. Wszelkie prawa zastrzeżone
