Carbocation Stability: Definition, Factors, Order

Carbocation Stability

A carbocation is a positively charged carbon atom that is cation. Carbocations are intermediates in many organic processes. They are typically unstable and short-lived, but can be sustained by resonance or nearby functional groups that can contribute electron density. Continue … Read more

Enolates and Formation of Enolates

Enolates and Formation of Enolates

Enolates have an essential role as organic reactive intermediates. They have the properties of both alkoxide and carbanion. Enolates may be made from carbonyl compounds like aldehydes and ketones by protonating the oxygen atom and then deprotonating the alpha-carbon atom. … Read more

Enantiomers vs Diastereomers: Differences and Similarities

Enantiomers vs Diastereomers

The main difference between enantiomers vs diastereomers is that enantiomers are found as mirror images whereas diastereomers are not. Enantiomers and diastereomers are two different types of stereoisomers. Stereoisomers are groups of molecules with identical connectivity and chemical composition but differing spatial arrangements … Read more

Types of Isomers

Types of isomers

There are two main types of isomers: structural isomers and stereoisomers. Isomers are structures that share the same molecular formula and chemical composition but have distinct atomic arrangements in space. Introduction to Isomer Isomers are chemical compounds that have the … Read more

Beckmann Rearrangement Reaction: Definition, Mechanism

Beckmann Rearrangement Reaction

The Beckmann rearrangement reaction, named after the German scientist Ernst Otto Beckmann (1853–1923), is an acid-catalyzed conversion of an oxime to an amide. In the synthesis of pharmaceuticals and natural compounds, the Beckmann rearrangement is a sophisticated transformation that is … Read more